A form of frontotemporal lobar degeneration and a progressive form of dementia characterized by motor speech impairment and AGRAMMATISM, with relative sparing of single word comprehension and semantic memory.
A progressive form of dementia characterized by the global loss of language abilities and initial preservation of other cognitive functions. Fluent and nonfluent subtypes have been described. Eventually a pattern of global cognitive dysfunction, similar to ALZHEIMER DISEASE, emerges. Pathologically, there are no Alzheimer or PICK DISEASE like changes, however, spongiform changes of cortical layers II and III are present in the TEMPORAL LOBE and FRONTAL LOBE. (From Brain 1998 Jan;121(Pt 1):115-26)
An aphasia characterized by impairment of expressive LANGUAGE (speech, writing, signs) and relative preservation of receptive language abilities (i.e., comprehension). This condition is caused by lesions of the motor association cortex in the FRONTAL LOBE (BROCA AREA and adjacent cortical and white matter regions).
A cognitive disorder marked by an impaired ability to comprehend or express language in its written or spoken form. This condition is caused by diseases which affect the language areas of the dominant hemisphere. Clinical features are used to classify the various subtypes of this condition. General categories include receptive, expressive, and mixed forms of aphasia.
The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight.
Heterogeneous group of neurodegenerative disorders characterized by frontal and temporal lobe atrophy associated with neuronal loss, gliosis, and dementia. Patients exhibit progressive changes in social, behavioral, and/or language function. Multiple subtypes or forms are recognized based on presence or absence of TAU PROTEIN inclusions. FTLD includes three clinical syndromes: FRONTOTEMPORAL DEMENTIA, semantic dementia, and PRIMARY PROGRESSIVE NONFLUENT APHASIA.
Tests designed to assess neurological function associated with certain behaviors. They are used in diagnosing brain dysfunction or damage and central nervous system disorders or injury.
An acquired organic mental disorder with loss of intellectual abilities of sufficient severity to interfere with social or occupational functioning. The dysfunction is multifaceted and involves memory, behavior, personality, judgment, attention, spatial relations, language, abstract thought, and other executive functions. The intellectual decline is usually progressive, and initially spares the level of consciousness.
Non-invasive method of demonstrating internal anatomy based on the principle that atomic nuclei in a strong magnetic field absorb pulses of radiofrequency energy and emit them as radiowaves which can be reconstructed into computerized images. The concept includes proton spin tomographic techniques.
A form of multiple sclerosis characterized by a progressive deterioration in neurologic function which is in contrast to the more typical relapsing remitting form. If the clinical course is free of distinct remissions, it is referred to as primary progressive multiple sclerosis. When the progressive decline is punctuated by acute exacerbations, it is referred to as progressive relapsing multiple sclerosis. The term secondary progressive multiple sclerosis is used when relapsing remitting multiple sclerosis evolves into the chronic progressive form. (From Ann Neurol 1994;36 Suppl:S73-S79; Adams et al., Principles of Neurology, 6th ed, pp903-914)
A language dysfunction characterized by the inability to name people and objects that are correctly perceived. The individual is able to describe the object in question, but cannot provide the name. This condition is associated with lesions of the dominant hemisphere involving the language areas, in particular the TEMPORAL LOBE. (From Adams et al., Principles of Neurology, 6th ed, p484)
Decrease in the size of a cell, tissue, organ, or multiple organs, associated with a variety of pathological conditions such as abnormal cellular changes, ischemia, malnutrition, or hormonal changes.
A verbal or nonverbal means of communicating ideas or feelings.
Tests designed to assess language behavior and abilities. They include tests of vocabulary, comprehension, grammar and functional use of language, e.g., Development Sentence Scoring, Receptive-Expressive Emergent Language Scale, Parsons Language Sample, Utah Test of Language Development, Michigan Language Inventory and Verbal Language Development Scale, Illinois Test of Psycholinguistic Abilities, Northwestern Syntax Screening Test, Peabody Picture Vocabulary Test, Ammons Full-Range Picture Vocabulary Test, and Assessment of Children's Language Comprehension.
A group of cognitive disorders characterized by the inability to perform previously learned skills that cannot be attributed to deficits of motor or sensory function. The two major subtypes of this condition are ideomotor (see APRAXIA, IDEOMOTOR) and ideational apraxia, which refers to loss of the ability to mentally formulate the processes involved with performing an action. For example, dressing apraxia may result from an inability to mentally formulate the act of placing clothes on the body. Apraxias are generally associated with lesions of the dominant PARIETAL LOBE and supramarginal gyrus. (From Adams et al., Principles of Neurology, 6th ed, pp56-7)
Loss or impairment of the ability to write (letters, syllables, words, or phrases) due to an injury to a specific cerebral area or occasionally due to emotional factors. This condition rarely occurs in isolation, and often accompanies APHASIA. (From Adams et al., Principles of Neurology, 6th ed, p485; APA, Thesaurus of Psychological Index Terms, 1994)
Communication through a system of conventional vocal symbols.
Treatment for individuals with speech defects and disorders that involves counseling and use of various exercises and aids to help the development of new speech habits.
The relationships between symbols and their meanings.
The most common clinical variant of MULTIPLE SCLEROSIS, characterized by recurrent acute exacerbations of neurologic dysfunction followed by partial or complete recovery. Common clinical manifestations include loss of visual (see OPTIC NEURITIS), motor, sensory, or bladder function. Acute episodes of demyelination may occur at any site in the central nervous system, and commonly involve the optic nerves, spinal cord, brain stem, and cerebellum. (Adams et al., Principles of Neurology, 6th ed, pp903-914)
A form of apraxia characterized by an acquired inability to carry out a complex motor activity despite the ability to mentally formulate the action. This condition has been attributed to a disruption of connections between the dominant parietal cortex and supplementary and premotor cortical regions in both hemispheres. (From Adams et al., Principles of Neurology, 6th ed, p57)

Making sense of progressive non-fluent aphasia: an analysis of conversational speech. (1/21)

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Familial Creutzfeldt-Jakob disease with a V180I mutation: comparative analysis with pathological findings and diffusion-weighted images. (2/21)

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Speech errors in progressive non-fluent aphasia. (3/21)

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Gray and white matter water diffusion in the syndromic variants of frontotemporal dementia. (4/21)

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Frontal lobe damage impairs process and content in semantic memory: evidence from category-specific effects in progressive non-fluent aphasia. (5/21)

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Why are patients with progressive nonfluent aphasia nonfluent? (6/21)

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Multimodal predictors for Alzheimer disease in nonfluent primary progressive aphasia. (7/21)

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Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis. (8/21)

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Primary Progressive Nonfluent Aphasia (PPNA) is a rare type of dementia that primarily affects language abilities. According to the National Aphasia Association, it is characterized by progressive difficulty with speaking and writing, while comprehension of single words and object knowledge remains relatively intact. The "nonfluent" descriptor refers to the hesitant, effortful, and halting speech pattern observed in individuals with this condition.

The Medical Subject Headings (MeSH) term provided by the National Library of Medicine defines PPNA as:

"A progressive aphasia characterized by agrammatism and/or anomia with relatively preserved single word comprehension and object knowledge. This condition often, but not always, begins between the sixth and seventh decades of life. As the disorder progresses, it may be accompanied by ideomotor apraxia, alien hand syndrome, and elements of corticobasal degeneration."

It is important to note that PPNA is a clinical diagnosis, and there are currently no established biomarkers or imaging techniques to definitively diagnose this condition. The underlying neuropathology may vary between individuals with PPNA, but the most common causes include frontotemporal lobar degeneration (FTLD) and corticobasal degeneration (CBD).

Primary Progressive Aphasia (PPA) is a neurological disorder characterized by progressive loss of language capabilities, while other cognitive abilities remain preserved. It is a type of dementia that primarily affects speech and language. Unlike other forms of aphasia that result from stroke or head injury, PPA is degenerative and gets worse over time.

There are three main types of PPA:

1. Semantic Variant PPA (svPPA): This type is characterized by difficulty in understanding words and objects, despite having no trouble with the mechanics of speech or writing. Over time, people with svPPA may lose their ability to understand spoken or written language, as well as to recognize objects and faces.

2. Nonfluent/Agrammatic Variant PPA (nfvPPA): This type is characterized by difficulty with speaking and writing, including producing grammatical sentences and articulating words. People with nfvPPA may also have problems with understanding spoken language, particularly when it comes to complex sentences or ambiguous phrases.

3. Logopenic Variant PPA (lvPPA): This type is characterized by difficulty with word-finding and sentence repetition, while speech remains fluent. People with lvPPA may also have problems with understanding spoken language, particularly when it comes to complex sentences or ambiguous phrases.

The exact cause of PPA is not known, but it is believed to be related to degeneration of specific areas of the brain involved in language processing, such as Broca's area and Wernicke's area. There is currently no cure for PPA, but speech and language therapy can help to slow down the progression of the disorder and improve communication skills.

Broca's aphasia, also known as expressive aphasia or nonfluent aphasia, is a type of language disorder that results from damage to the brain's Broca's area, which is located in the frontal lobe of the dominant hemisphere (usually the left).

Individuals with Broca's aphasia have difficulty producing spoken or written language. They often know what they want to say but have trouble getting the words out, resulting in short and grammatically simplified sentences. Speech may be slow, laborious, and agrammatic, with limited vocabulary and poor sentence structure. Comprehension of language is typically less affected than expression, although individuals with Broca's aphasia may have difficulty understanding complex grammatical structures or following rapid speech.

It's important to note that the severity and specific symptoms of Broca's aphasia can vary depending on the extent and location of the brain damage. Rehabilitation and therapy can help improve language skills in individuals with Broca's aphasia, although recovery may be slow and limited.

Aphasia is a medical condition that affects a person's ability to communicate. It is caused by damage to the language areas of the brain, most commonly as a result of a stroke or head injury. Aphasia can affect both spoken and written language, making it difficult for individuals to express their thoughts, understand speech, read, or write.

There are several types of aphasia, including:

1. Expressive aphasia (also called Broca's aphasia): This type of aphasia affects a person's ability to speak and write clearly. Individuals with expressive aphasia know what they want to say but have difficulty forming the words or sentences to communicate their thoughts.
2. Receptive aphasia (also called Wernicke's aphasia): This type of aphasia affects a person's ability to understand spoken or written language. Individuals with receptive aphasia may struggle to follow conversations, comprehend written texts, or make sense of the words they hear or read.
3. Global aphasia: This is the most severe form of aphasia and results from extensive damage to the language areas of the brain. People with global aphasia have significant impairments in both their ability to express themselves and understand language.
4. Anomic aphasia: This type of aphasia affects a person's ability to recall the names of objects, people, or places. Individuals with anomic aphasia can speak in complete sentences but often struggle to find the right words to convey their thoughts.

Treatment for aphasia typically involves speech and language therapy, which aims to help individuals regain as much communication ability as possible. The success of treatment depends on various factors, such as the severity and location of the brain injury, the individual's motivation and effort, and the availability of support from family members and caregivers.

Frontotemporal dementia (FTD) is a group of disorders caused by progressive degeneration of the frontal and temporal lobes of the brain. These areas of the brain are associated with personality, behavior, and language.

There are three main types of FTD:

1. Behavioral variant FTD (bvFTD): This type is characterized by changes in personality, behavior, and judgment. Individuals may become socially inappropriate, emotionally indifferent, or impulsive. They may lose interest in things they used to enjoy and have difficulty with tasks that require planning and organization.

2. Primary progressive aphasia (PPA): This type affects language abilities. There are two main subtypes of PPA: semantic dementia and progressive nonfluent aphasia. Semantic dementia is characterized by difficulty understanding words and objects, while progressive nonfluent aphasia is characterized by problems with speech production and articulation.

3. Motor neuron disease (MND) associated FTD: Some individuals with FTD may also develop motor neuron disease, which affects the nerves that control muscle movement. This can lead to weakness, stiffness, and wasting of muscles, as well as difficulty swallowing and speaking.

FTD is a degenerative disorder, meaning that symptoms get worse over time. There is no cure for FTD, but there are treatments available to help manage symptoms and improve quality of life. The exact cause of FTD is not known, but it is believed to be related to abnormalities in certain proteins in the brain. In some cases, FTD may run in families and be caused by genetic mutations.

Frontotemporal lobar degeneration (FTLD) is a group of disorders characterized by the progressive degeneration of the frontal and temporal lobes of the brain. These areas of the brain are involved in decision-making, behavior, emotion, and language. FTLD can be divided into several subtypes based on the specific clinical features and the underlying protein abnormalities.

The three main subtypes of FTLD are:

1. Behavioral variant frontotemporal dementia (bvFTD): This subtype is characterized by changes in personality, behavior, and judgment. People with bvFTD may lose their social inhibitions, become impulsive, or develop compulsive behaviors. They may also have difficulty with emotional processing and empathy.
2. Primary progressive aphasia (PPA): This subtype is characterized by the gradual deterioration of language skills. People with PPA may have difficulty speaking, understanding spoken or written language, or both. There are three subtypes of PPA: nonfluent/agrammatic variant, semantic variant, and logopenic variant.
3. Motor neuron disease (MND) with FTLD: This subtype is characterized by the degeneration of motor neurons, which are the nerve cells responsible for controlling voluntary muscle movements. People with MND with FTLD may develop symptoms of amyotrophic lateral sclerosis (ALS), such as muscle weakness, stiffness, and twitching, as well as cognitive and behavioral changes associated with FTLD.

The underlying protein abnormalities in FTLD include:

1. Tau protein: In some forms of FTLD, the tau protein accumulates and forms clumps called tangles inside nerve cells. This is also seen in Alzheimer's disease.
2. TDP-43 protein: In other forms of FTLD, the TDP-43 protein accumulates and forms clumps inside nerve cells.
3. Fused in sarcoma (FUS) protein: In a small number of cases, the FUS protein accumulates and forms clumps inside nerve cells.

FTLD is typically a progressive disorder, meaning that symptoms worsen over time. There is currently no cure for FTLD, but there are treatments available to help manage symptoms and improve quality of life.

Neuropsychological tests are a type of psychological assessment that measures cognitive functions, such as attention, memory, language, problem-solving, and perception. These tests are used to help diagnose and understand the cognitive impact of neurological conditions, including dementia, traumatic brain injury, stroke, Parkinson's disease, and other disorders that affect the brain.

The tests are typically administered by a trained neuropsychologist and can take several hours to complete. They may involve paper-and-pencil tasks, computerized tasks, or interactive activities. The results of the tests are compared to normative data to help identify any areas of cognitive weakness or strength.

Neuropsychological testing can provide valuable information for treatment planning, rehabilitation, and assessing response to treatment. It can also be used in research to better understand the neural basis of cognition and the impact of neurological conditions on cognitive function.

Dementia is a broad term that describes a decline in cognitive functioning, including memory, language, problem-solving, and judgment, severe enough to interfere with daily life. It is not a specific disease but rather a group of symptoms that may be caused by various underlying diseases or conditions. Alzheimer's disease is the most common cause of dementia, accounting for 60-80% of cases. Other causes include vascular dementia, Lewy body dementia, frontotemporal dementia, and Huntington's disease.

The symptoms of dementia can vary widely depending on the cause and the specific areas of the brain that are affected. However, common early signs of dementia may include:

* Memory loss that affects daily life
* Difficulty with familiar tasks
* Problems with language or communication
* Difficulty with visual and spatial abilities
* Misplacing things and unable to retrace steps
* Decreased or poor judgment
* Withdrawal from work or social activities
* Changes in mood or behavior

Dementia is a progressive condition, meaning that symptoms will gradually worsen over time. While there is currently no cure for dementia, early diagnosis and treatment can help slow the progression of the disease and improve quality of life for those affected.

Medical Definition:

Magnetic Resonance Imaging (MRI) is a non-invasive diagnostic imaging technique that uses a strong magnetic field and radio waves to create detailed cross-sectional or three-dimensional images of the internal structures of the body. The patient lies within a large, cylindrical magnet, and the scanner detects changes in the direction of the magnetic field caused by protons in the body. These changes are then converted into detailed images that help medical professionals to diagnose and monitor various medical conditions, such as tumors, injuries, or diseases affecting the brain, spinal cord, heart, blood vessels, joints, and other internal organs. MRI does not use radiation like computed tomography (CT) scans.

Multiple Sclerosis (MS), Chronic Progressive is a form of Multiple Sclerosis, a chronic autoimmune disease that affects the central nervous system (CNS). In this form, the disease follows a steady progression with no distinct relapses or remissions. The symptoms worsen over time, leading to a decline in physical functioning and increased disability.

The term "chronic progressive" is used to describe the course of the disease, which is characterized by a continuous worsening of neurological functions from the onset, or after an initial relapsing-remitting phase. There are two types of chronic progressive MS: primary and secondary.

1. Primary Chronic Progressive MS (PCP): This form of MS shows a steady progression of symptoms from the beginning, with no distinct remissions or relapses. The disability accumulates gradually over time, and the person may experience varying degrees of physical and cognitive impairment.

2. Secondary Chronic Progressive MS (SCP): In this form, an individual initially has a relapsing-remitting course of MS (RRMS), characterized by unpredictable relapses followed by periods of partial or complete recovery (remissions). However, after some time, the disease transitions to a steady progression of symptoms and disability, even without distinct relapses. This is known as secondary chronic progressive MS.

The exact cause of Multiple Sclerosis remains unknown; however, it is believed to be influenced by genetic, environmental, and immunological factors. The disease involves the immune system attacking the myelin sheath, a protective covering surrounding nerve fibers in the CNS. This results in lesions or scars (scleroses) that disrupt communication between the brain, spinal cord, and other parts of the body, leading to various physical, cognitive, and sensory symptoms.

Management of Chronic Progressive MS typically involves a multidisciplinary approach, focusing on symptom management, rehabilitation, and maintaining quality of life. Currently, there are no approved disease-modifying therapies specifically for chronic progressive MS; however, some medications used to treat relapsing-remitting MS may help slow the progression of disability in certain individuals with secondary chronic progressive MS.

Anomia is a language disorder that affects a person's ability to name objects, places, or people. It is often caused by damage to the brain, such as from a stroke, brain injury, or neurological condition. In anomia, a person has difficulty retrieving words from their memory, and may substitute similar-sounding words, describe the object instead of naming it, or be unable to come up with a name at all. Anomia can range from mild to severe and can significantly impact a person's ability to communicate effectively.

Atrophy is a medical term that refers to the decrease in size and wasting of an organ or tissue due to the disappearance of cells, shrinkage of cells, or decreased number of cells. This process can be caused by various factors such as disuse, aging, degeneration, injury, or disease.

For example, if a muscle is immobilized for an extended period, it may undergo atrophy due to lack of use. Similarly, certain medical conditions like diabetes, cancer, and heart failure can lead to the wasting away of various tissues and organs in the body.

Atrophy can also occur as a result of natural aging processes, leading to decreased muscle mass and strength in older adults. In general, atrophy is characterized by a decrease in the volume or weight of an organ or tissue, which can have significant impacts on its function and overall health.

In the context of medicine, particularly in neurolinguistics and speech-language pathology, language is defined as a complex system of communication that involves the use of symbols (such as words, signs, or gestures) to express and exchange information. It includes various components such as phonology (sound systems), morphology (word structures), syntax (sentence structure), semantics (meaning), and pragmatics (social rules of use). Language allows individuals to convey their thoughts, feelings, and intentions, and to understand the communication of others. Disorders of language can result from damage to specific areas of the brain, leading to impairments in comprehension, production, or both.

A language test is not a medical term per se, but it is commonly used in the field of speech-language pathology, which is a medical discipline. A language test, in this context, refers to an assessment tool used by speech-language pathologists to evaluate an individual's language abilities. These tests typically measure various aspects of language, including vocabulary, grammar, syntax, semantics, and pragmatics.

Language tests can be standardized or non-standardized and may be administered individually or in a group setting. The results of these tests help speech-language pathologists diagnose language disorders, develop treatment plans, and monitor progress over time. It is important to note that language testing should be conducted by a qualified professional who has experience in administering and interpreting language assessments.

Apraxia is a motor disorder characterized by the inability to perform learned, purposeful movements despite having the physical ability and mental understanding to do so. It is not caused by weakness, paralysis, or sensory loss, and it is not due to poor comprehension or motivation.

There are several types of apraxias, including:

1. Limb-Kinematic Apraxia: This type affects the ability to make precise movements with the limbs, such as using tools or performing complex gestures.
2. Ideomotor Apraxia: In this form, individuals have difficulty executing learned motor actions in response to verbal commands or visual cues, but they can still perform the same action when given the actual object to use.
3. Ideational Apraxia: This type affects the ability to sequence and coordinate multiple steps of a complex action, such as dressing oneself or making coffee.
4. Oral Apraxia: Also known as verbal apraxia, this form affects the ability to plan and execute speech movements, leading to difficulties with articulation and speech production.
5. Constructional Apraxia: This type impairs the ability to draw, copy, or construct geometric forms and shapes, often due to visuospatial processing issues.

Apraxias can result from various neurological conditions, such as stroke, brain injury, dementia, or neurodegenerative diseases like Parkinson's disease and Alzheimer's disease. Treatment typically involves rehabilitation and therapy focused on retraining the affected movements and compensating for any residual deficits.

Agraphia is a neurological disorder that affects the ability to write, either by hand or through mechanical means like typing. It is often caused by damage to specific areas of the brain involved in language and writing skills, such as the left parietal lobe. Agraphia can manifest as difficulty with spelling, forming letters or words, organizing thoughts on paper, or expressing ideas in writing. Depending on the severity and location of the brain injury, agraphia may occur in isolation or alongside other language or cognitive impairments.

Speech is the vocalized form of communication using sounds and words to express thoughts, ideas, and feelings. It involves the articulation of sounds through the movement of muscles in the mouth, tongue, and throat, which are controlled by nerves. Speech also requires respiratory support, phonation (vocal cord vibration), and prosody (rhythm, stress, and intonation).

Speech is a complex process that develops over time in children, typically beginning with cooing and babbling sounds in infancy and progressing to the use of words and sentences by around 18-24 months. Speech disorders can affect any aspect of this process, including articulation, fluency, voice, and language.

In a medical context, speech is often evaluated and treated by speech-language pathologists who specialize in diagnosing and managing communication disorders.

Speech Therapy, also known as Speech-Language Pathology, is a medical field that focuses on the assessment, diagnosis, treatment, and prevention of communication and swallowing disorders in children and adults. These disorders may include speech sound production difficulties (articulation disorders or phonological processes disorders), language disorders (expressive and/or receptive language impairments), voice disorders, fluency disorders (stuttering), cognitive-communication disorders, and swallowing difficulties (dysphagia).

Speech therapists, who are also called speech-language pathologists (SLPs), work with clients to improve their communication abilities through various therapeutic techniques and exercises. They may also provide counseling and education to families and caregivers to help them support the client's communication development and management of the disorder.

Speech therapy services can be provided in a variety of settings, including hospitals, clinics, schools, private practices, and long-term care facilities. The specific goals and methods used in speech therapy will depend on the individual needs and abilities of each client.

I'm sorry for any confusion, but "semantics" is not a term that has a specific medical definition. Semantics is actually a branch of linguistics that deals with the study of meaning, reference, and the interpretation of signs and symbols, either individually or in combination. It is used in various fields including computer science, anthropology, psychology, and philosophy.

However, if you have any medical terms or concepts that you would like me to explain, I'd be happy to help!

Relapsing-remitting multiple sclerosis (RRMS) is a type of multiple sclerosis (MS), which is a chronic autoimmune disease that affects the central nervous system (CNS). In RRMS, the immune system attacks the protective covering of nerve fibers (myelin sheath) in the CNS, leading to the formation of lesions or scars (scleroses). These attacks result in episodes of new or worsening symptoms, known as relapses or exacerbations.

The distinguishing feature of RRMS is that these relapses are followed by periods of partial or complete recovery (remissions), during which symptoms may improve, stabilize, or even disappear temporarily. The duration and severity of relapses and remissions can vary significantly among individuals with RRMS. Over time, the accumulation of damage to the nervous system can lead to progressive disability.

Approximately 85% of people with MS are initially diagnosed with the relapsing-remitting form. With appropriate treatment and management, many people with RRMS can effectively manage their symptoms and maintain a good quality of life for several years.

Ideomotor apraxia is a neurological disorder that affects the ability to perform learned, purposeful movements in the absence of muscle weakness or paralysis. It results from damage to specific areas of the brain that are responsible for motor planning and execution.

In ideomotor apraxia, the person has difficulty translating an intention or idea into the appropriate movement. For example, if asked to pantomime using a toothbrush, they may not be able to recall and execute the correct sequence of movements required for this task, even though they understand what is being asked of them and have no problem moving their arm or hand.

This disorder can manifest as awkward, poorly coordinated, or incomplete movements, often with inconsistent errors. Ideomotor apraxia is typically seen following lesions to the left hemisphere of the brain, particularly in regions associated with language and motor function, such as Broca's area and the parietal lobe. Treatment usually involves occupational therapy and strategies to help compensate for the impaired motor skills.

Agramatic variant of primary progressive aphasia. *Non-fluent variant PPA. *Prevalence: 1-9 / 100 000 ... Progressive non-fluent aphasia. Disease definition Progressive non-fluent aphasia (PNFA) is a form of frontotemporal dementia ( ...
... S. M. Wilson;N. F. Dronkers; ... In the nonfluent variant of primary progressive aphasia (PPA), degeneration of the posterior IFC is associated with expressive ... In the nonfluent variant of primary progressive aphasia (PPA), degeneration of the posterior IFC is associated with expressive ... In nonfluent PPA patients, the posterior IFC was atrophic and, unlike controls, showed an equivalent level of functional ...
... which he called primary progressive aphasia (PPA) included patients with progressive nonfluent (aphasia, semantic dementia, and ... "The new classification of primary progressive aphasia into semantic, logopenic, or nonfluent/agrammatic variants". Current ... Progressive nonfluent aphasia (PNFA) is one of three clinical syndromes associated with frontotemporal lobar degeneration. PNFA ... Based on these imaging methods, progressive nonfluent aphasia can be regionally dissociated from the other subtypes of ...
Primary Progressive Nonfluent Aphasia / pathology Grants and funding * P30 HD003110/HD/NICHD NIH HHS/United States ... and 9 progressive nonfluent aphasia (PNFA)] and 21 controls. Compared to controls, SD displayed severe atrophy of the whole ...
What Is Non-Fluent Primary Progressive Aphasia?. Medically reviewed by Alana Biggers, M.D., MPH ... Swallowing may become a challenge for people with primary progressive aphasia. Learn here how to manage the symptom. ...
Progressive non-fluent aphasia People with this condition have trouble speaking and make mistakes in how they say words or ... Information in this booklet is for anyone who wants to know more about primary progressive aphasia (PPA). This includes people ... With all types of primary progressive aphasia (PPA), speech and language are affected first. Symptoms vary depending on what ... People with logopenic aphasia have trouble finding the words they want to use. For example, they may:. *Have trouble ...
... memory.ucsf.edu/dementia/primary-progressive-aphasia/nonfluent-variant-primary-progressive-aphasia ... Loss of language skills commonly present as aphasia:[4][5]. *Primary progressive aphasia involves trouble finding words and ... Primary progressive aphasia - Known as PPA, this type of FTD degeneration focuses on the loss of language abilities in both the ... Progressive nonfluent aphasia - Known as nfvPPA, this type of FTD dementia affects ones ability to produce speech, which ...
... non-fluent variant primary progressive aphasia; svPPA, semantic variant primary progressive aphasia. ... eight with semantic variant primary progressive aphasia (svPPA), five with non-fluent variant primary progressive aphasia ( ... svPPA and non-fluent variant primary progressive aphasia (nfvPPA). Flavour identification was assessed using a new battery, in ... Classification of primary progressive aphasia and its variants. Neurology 2011;76:1006-14. ...
progressive nonfluent aphasia; PPA=. primary progressive aphasia; rc=. repeat counts; SNP=. single nucleotide polymorphism. ... the latter is subdivided into semantic dementia or semantic variant PPA and progressive nonfluent aphasia (PNFA) or nonfluent/ ... Classification of primary progressive aphasia and its variants. Neurology 2011;76:1006-1014. ... Genetic screen in a large series of patients with primary progressive aphasia. Alzheimers Dement 2019;15:553-560. ...
However, her prominent memory decline prompted a revised diagnosis of logopenic variant of primary progressive aphasia due to ... She was originally diagnosed with the FTD subtype, progressive nonfluent aphasia. ... Primary Papers. * Levy-Lahad E, Wasco W, Poorkaj P, Romano DM, Oshima J, Pettingell WH, Yu CE, Jondro PD, Schmidt SD, Wang K. ... One mutation carrier developed progressive dementia at age 51 and died at age 61 following a disease characterized by memory ...
Three participants with progressive agrammatism participated (n=2 with nonfluent/agrammatic primary progressive aphasia, or ... Findings support the utility of implicit modes of training for syntax production in agrammatic progressive aphasia, consistent ... Retraining Syntactic Structures via Script Training in Progressive Aphasia: Evidence for Implicit Learning in Agrammatism. ... Retraining Syntactic Structures via Script Training in Progressive Aphasia: Evidence for Implicit Learning in Agrammatism}, ...
Non-fluent/agrammatic variant primary progressive aphasia (nfvPPA). There is a third form of primary progressive aphasia (PPA) ... A Healthcare Providers Guide to the Nonfluent Variant of Primary Progressive Aphasia (PDF) ... A Healthcare Providers Guide to the Semantic Variant of Primary Progressive Aphasia (PDF) ... called logopenic variant primary progressive aphasia (lvPPA). At autopsy, patients with lvPPA are often found to have ...
Patterns of language decline in non-fluent primary progressive aphasia. CK Thompson, KJ Ballard, ME Tait, S Weintraub, M ... speech and phonological errors in the diagnosis of nonfluent/agrammatic and logopenic variants of primary progressive aphasia. ... Subtypes of progressive aphasia: application of the international consensus criteria and validation using β-amyloid imaging. CE ... Training and Generalized Production of wh- and NP-Movement Structures in Agrammatic Aphasia. CK Thompson, LP Shapiro, KJ ...
As the condition worsened she was referred to a behavioral neurologist who diagnosed primary progressive aphasia, non-fluent ... A. Primary progressive aphasia (PPA) is a language disorder that affects a persons ability to speak, read, write and ... PPA is distinct from aphasia caused by stroke. In 2011, PPA was reclassified into three clinical subtypes: nonfluent/agrammatic ... Q: If non-fluent/agrammatic is one type of PPA, what are the others? How do the subtypes differ? ...
Findings of Impaired Hearing in Patients with Nonfluent/Agrammatic Variant Primary Progressive Aphasia. JAMA Neurol. 2019;76: ... Alzheimers Disease (AD) is an acquired condition characterized by progressive cognitive and behavioural decline and is the ... Synaptopathy in the noise-exposed and aging cochlea: Primary neural degeneration in acquired sensorineural hearing loss. Hear ...
Healthy brain connectivity predicts atrophy progression in non-fluent variant of primary progressive aphasia. Brain. 2016 10; ... White matter damage in primary progressive aphasias: a diffusion tensor tractography study. Brain. 2011 Oct; 134(Pt 10):3011-29 ... Frontal white matter tracts sustaining speech production in primary progressive aphasia. J Neurosci. 2014 Jul 16; 34(29):9754- ... Onset of secondary progressive MS after long-term rituximab therapy - a case report. Ann Clin Transl Neurol. 2017 Jan; 4(1):46- ...
Cases of elderly patients with progressive language deterioration have been described since Arnold Picks landmark case report ... Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis. Neurology. 2010 Aug 17. 75(7):603- ... Progressive nonfluent aphasia. In progressive nonfluent aphasia, speech is effortful and halting, with phoneme or speech sound ... Primary Progressive Aphasia. For the subgroup of patients with frontotemporal lobe dementia (FTD) who have primary progressive ...
Their clinical diagnoses range from FTD, AD, PD, primary progressive aphasia (PPA), and progressive nonfluent aphasia (PNFA)- ...
Non-verbal auditory impairment is increasingly recognised in the primary progressive aphasias (PPAs) but its relationship to ... nfvPPA patient group with non-fluent primary progressive aphasia, svPPA patient group with semantic variant primary progressive ... Receptive prosody in nonfluent primary progressive aphasias. Cortex. 2012;48:308-16. ... Delayed auditory feedback simulates features of nonfluent primary progressive aphasia. J Neurol Sci. 2014;347:345-8. ...
Cases of elderly patients with progressive language deterioration have been described since Arnold Picks landmark case report ... Syndromes of nonfluent primary progressive aphasia: a clinical and neurolinguistic analysis. Neurology. 2010 Aug 17. 75(7):603- ... Progressive nonfluent aphasia. In progressive nonfluent aphasia, speech is effortful and halting, with phoneme or speech sound ... Primary Progressive Aphasia. For the subgroup of patients with frontotemporal lobe dementia (FTD) who have primary progressive ...
Symptom-led staging for semantic and non-fluent/agrammatic variants of primary progressive aphasia  Hardy, CJD; Taylor-Rubin, ...
... progressive non-fluent aphasia (speech disorder), and Alzheimers disease - to rate how much the participants liked and were ... A recent study in the United Kingdom asked the primary caregivers of people with different subtypes of dementia - ...
... is a progressive neurodegenerative disease of the frontal and/or temporal lobe generally caused by mutations to proteins in the ... Two variants of primary progressive aphasia (PPA): * Progressive nonfluent aphasia (PNFA; also known as nonfluent agrammatic ... variant primary progressive aphasia) * Semantic dementia (SD; fluent type, also known as semantic variant primary progressive ... Progressive Non Fluent Aphasia (PNFA): language impairment (e.g., grammatical errors, apraxia). * Semantic dementia (SD): ...
Semantic and lexical features of words dissimilarly affected by non-fluent, logopenic, and semantic primary progressive aphasia ... with a focus on Alzheimers disease and primary progressive aphasia. Previous work has focused on detecting subtle semantic ... Systematic review of subjective memory measures to inform assessing memory limitations after stroke and stroke-related aphasia ...
Patterns of language decline in non-fluent primary progressive aphasia. [Journal (Paginated)] ... Murray, L. L. and Holland, A. L. and Beeson, P. M. (1997) Accuracy monitoring and task demand evaluation in aphasia. [Journal ( ... Wertz, R. T. and Auther, L. L. and Ross, K. B. (1997) Aphasia in African-Americans and Caucasians: Severity, improvement, and ... Marshall, R. C. and Freed, D. B. and Phillips, D. S. (1997) Communicative efficiency in severe aphasia. [Journal (Paginated)] ...
5. Motor speech disorders in the nonfluent, semantic and logopenic variants of primary progressive aphasia. Supplementary data ...
The spectrum of sporadic frontotemporal lobar degeneration associated with tau pathology includes progressive supranuclear ... progressive supranuclear palsy, corticobasal degeneration and Picks disease. ... resulting in a progressive accumulation of intracellular tau aggregates. ... Atypical variants of PSP include frontotemporal dementia (FTD) [46], nonfluent/agrammatic primary progressive aphasia and ...
Multimodal 18F-AV-1451 and MRI findings in nonfluent variant of primary progressive aphasia: Possible insights on nodal ... Posterior primary progressive prosopagnosia: Structural and molecular imaging. Pascual, B., Masdeu, J. C., Funk, Q., Zanotti- ...
  • Progressive nonfluent aphasia (PNFA) is one of three clinical syndromes associated with frontotemporal lobar degeneration. (wikipedia.org)
  • PNFA has an insidious onset of language deficits over time as opposed to other stroke-based aphasias, which occur acutely following trauma to the brain. (wikipedia.org)
  • The subjects included 19 AD and 35 FTLD patients [13 frontotemporal dementia (FTD), 13 semantic dementia (SD), and 9 progressive nonfluent aphasia (PNFA)] and 21 controls. (nih.gov)
  • Their clinical diagnoses range from FTD, AD, PD, primary progressive aphasia (PPA), and progressive nonfluent aphasia (PNFA)-all from having inherited the same mutation. (alzforum.org)
  • Two types make up PPA: semantic dementia (SD) and progressive non-fluent aphasia (PNFA). (rarerevolutionmagazine.com)
  • Progressive nonfluent aphasia - Known as nfvPPA, this type of FTD dementia affects one's ability to produce speech, which becomes increasingly halting. (mentalhealth.com)
  • Methods We studied flavour identification prospectively in 25 patients with FTLD (12 with behavioural variant frontotemporal dementia (bvFTD), eight with semantic variant primary progressive aphasia (svPPA), five with non-fluent variant primary progressive aphasia (nfvPPA)) and 17 healthy control subjects, using a new test based on cross-modal matching of flavours to words and pictures. (bmj.com)
  • Based on these imaging methods, progressive nonfluent aphasia can be regionally dissociated from the other subtypes of frontotemporal lobar degeneration, frontotemporal dementia and semantic dementia. (wikipedia.org)
  • Mesulam's original description in 1982 of progressive language problems caused by neurodegenerative disease (which he called primary progressive aphasia (PPA) included patients with progressive nonfluent (aphasia, semantic dementia, and logopenic progressive aphasia. (wikipedia.org)
  • However, as research shed light on this condition and related neurodegenerative diseases, Pick's disease was grouped with semantic dementia and primary progressive aphasia under the umbrella term frontotemporal dementia. (mentalhealth.com)
  • 1-6 Impairments of flavour processing and particularly flavour agnosia have been associated with focal anterior temporal lobe damage and, in the neurodegenerative disease spectrum, with frontotemporal lobar degeneration (FTLD), especially the syndrome of semantic dementia or semantic variant primary progressive aphasia (svPPA). (bmj.com)
  • One mutation carrier developed progressive dementia at age 51 and died at age 61 following a disease characterized by memory loss, rigidity, and generalized tonic-clonic seizures. (alzforum.org)
  • Frontotemporal dementia (FTD) is a group of related conditions resulting from the progressive degeneration of the temporal and frontal lobes of the brain. (ucsf.edu)
  • Alzheimer's Disease (AD) is an acquired condition characterized by progressive cognitive and behavioural decline and is the second most common form of dementia in the general population after mild cognitive impairment[ 1 ]. (tinnitusjournal.com)
  • In 1982, Mesulam reported 6 patients with progressive aphasia, gradually worsening over a number of years, who did not develop a more generalized dementia. (medscape.com)
  • Subsequently, the PPA syndrome was defined as a disorder limited to progressive aphasia, without general cognitive impairment or dementia, over a 2-year period. (medscape.com)
  • In England and Europe, cases of frontal lobe dementia were described with progressive dysfunction of the frontal lobes. (medscape.com)
  • The condition described in the North American literature as primary progressive aphasia and that described in the European literature as frontal dementia have been combined under the term frontotemporal lobe dementia (FTD) or frontotemporal lobar degeneration (FTLD). (medscape.com)
  • The progressive aphasias have been divided into 3 groups: progressive nonfluent aphasia, semantic dementia, and logopenic progressive aphasia. (medscape.com)
  • In recent years, the term frontotemporal dementia has become an umbrella term referring to clinical syndromes of frontal dementia or progressive aphasia. (medscape.com)
  • A recent study in the United Kingdom asked the primary caregivers of people with different subtypes of dementia - frontotemporal , semantic, progressive non-fluent aphasia (speech disorder), and Alzheimer's disease - to rate how much the participants liked and were exposed to different types of humor. (dementia.org)
  • Frontotemporal dementia (FTD) is a progressive neurodegenerative disease of the frontal and/or temporal lobe generally caused by mutations to proteins in the brain (e.g. (amboss.com)
  • Her overall goal is to investigate the evolution of language use and cognitive decline throughout the course of dementia to help accurate and timely diagnosis, with a focus on Alzheimer's disease and primary progressive aphasia. (ucsf.edu)
  • Frontotemporal dementia (FTD) is a progressive neurodegenerative condition characterized by clinical, genetic and neuropathologic heterogeneity. (biomedcentral.com)
  • His Clinical psychology research incorporates themes from Epidemiology, Progressive nonfluent aphasia, Semantic dementia, Primary progressive aphasia and Comorbidity. (research.com)
  • His primary areas of study are Neuroscience, Cognitive psychology, Frontotemporal dementia, Interoception and Brain network. (research.com)
  • Under the primary progressive aphasias there are two subtypes: progressive nonfluent aphasia and semantic dementia. (rarerevolutionmagazine.com)
  • Language deficits in major forms of dementia and primary progressive aphasias: an update according to new diagnostic criteria]. (ulaval.ca)
  • Atypical Parkinsonism affects about five to ten percent of patients with Parkinsonism and includes the diseases Corticobasal Degeneration, Progressive Supranuclear Palsy, Lewy Body Dementia and Multiple System Atrophy. (bz-bx.net)
  • Atypical Parkinsonian syndromes (APS) feature a heterogeneous group of progressive neurodegenerative diseases, to which multiple system atrophy (MSA), dementia with Lewy bodies (DLB), progressive supranuclear palsy (PSP) and corticobasal degeneration (CBD) are counted. (bz-bx.net)
  • Pick disease (named after Arnold Pick) is a progressive dementia defined by clinical and pathologic criteria. (medscape.com)
  • Two types of primary progressive aphasia are identified: (1) semantic dementia, in which meaning systems are lost from language, and (2) nonfluent primary progressive aphasia. (medscape.com)
  • There is a growing population of individuals diagnosed with various forms of Frontotemporal Dementia (FTD) and Primary Progressive Aphasia (PPA), and this number is likely to increase as medical practitioners and speech-language pathologists (SLPs) become more expert at identifying these conditions. (edu.au)
  • Progressive supranuclear palsy is a rare, degenerative central nervous system disorder that progressively impairs voluntary eye movements and causes bradykinesia, muscular rigidity with progressive axial dystonia, pseudobulbar palsy, and dementia. (msdmanuals.com)
  • Language deficits in Alzheimer's disease and in nonfluent/agrammatic and semantic variants of primary progressive aphasia are well documented. (ulaval.ca)
  • Motor speech disorders in the nonfluent, semantic and logopenic variants of primary progressive aphasia. (uni-muenchen.de)
  • Language deficits are also the core features of three variants of primary progressive aphasia, namely the nonfluent/agrammatic, semantic and logopenic variants. (ulaval.ca)
  • Apraxia of speech (AOS) is a core diagnostic feature of nonfluent/agrammatic primary progressive aphasia (naPPA). (pennftdcenter.org)
  • Each chapter provides a comprehensive outline of testing that will assist in the diagnosis of the cognitive-communication disorders associated with FTD, PPAs, and primary progressive apraxia of speech (PPAOS). (edu.au)
  • Hematoxylin and eosin stain of the left frontal cortex from a patient with primary progressive aphasia. (medscape.com)
  • His Cognitive psychology research incorporates elements of Primary progressive aphasia and Frontal lobe. (research.com)
  • However, her prominent memory decline prompted a revised diagnosis of logopenic variant of primary progressive aphasia due to AD. (alzforum.org)
  • The identification of logopenic variant of primary progressive aphasia is very recent, and more research is needed to complete the clinical description and identification of the functional origin of the disorders. (ulaval.ca)
  • His case study "On the relationship between aphasia and senile atrophy of the brain" still serves as a frame of reference for apparently focal brain syndromes in diffuse or generalized degenerative diseases of the brain. (medscape.com)
  • As the condition worsened she was referred to a behavioral neurologist who diagnosed primary progressive aphasia, non-fluent type (PPA), also known as "agrammatic PPA. (theaftd.org)
  • We conclude that in nonfluent PPA, the posterior IFC is not only structurally damaged, but also functionally abnormal, suggesting a critical role for this region in the breakdown of syntactic processing in this syndrome. (unitn.it)
  • Corticobasal syndrome (CBS), also called corticobasal degeneration (CBD), and progressive supranuclear palsy (PSP) are two related diseases that are not classified as FTD but often share symptoms with FTD. (ucsf.edu)
  • A surprising finding of this investigation is that AOS is not associated with an underlying motor disorder such as corticobasal syndrome or progressive supranuclear palsy. (pennftdcenter.org)
  • Definition: Multiple system atrophy (MSA) is a progressive, neurodegenerative disease, which may present clinically in the form of autonomous dysfunction, Parkinsonian syndrome, cerebellar symptoms or pyramidal tract signs. (bz-bx.net)
  • Primary progressive aphasia is a focal atrophy syndrome that may be associated with Pick disease, Alzheimer disease, or other pathology. (medscape.com)
  • People with learning disabilities such as dyslexia may be at higher risk of FTD, but it is not known whether this is generally true or if it is true only for certain patterns of learning disability and, whether only certain types of symptoms, such as the syndrome complex of primary progressive aphasia, may be more common in people with a learning disability history. (medscape.com)
  • The main clinical features are signature language progressive difficulties with speech production. (wikipedia.org)
  • Because the biofluid arm participants do not undergo the same detailed clinical and functional assessments required for the longitudinal arm, participants may be included regardless of primary language, as long as an appropriately translated consent is available. (ucsf.edu)
  • Primary Progressive Aphasia and Other Frontotemporal Dementias is targeted toward practicing clinicians, graduate students, and clinical researchers who are interested in the latest conceptualization of FTD spectrum disorders. (edu.au)
  • The primary progressive aphasias (PPAs) continue to present substantial problems of classification and diagnosis. (biomedcentral.com)
  • Primary Progressive Aphasia and Other Frontotemporal Dementias: Diagnosis and Treatment of Associated Communication Disorders is the second volume in the 'Medical Speech-Language Pathology' book series. (edu.au)
  • Aphasia -- Diagnosis. (edu.au)
  • Using structural and functional magnetic resonance imaging, we quantified tissue volumes and functional responses to a syntactic comprehension task in eight patients with nonfluent PPA, compared to healthy age-matched controls. (unitn.it)
  • In nonfluent PPA patients, the posterior IFC was atrophic and, unlike controls, showed an equivalent level of functional activity for syntactically complex and simpler sentences. (unitn.it)
  • [ 1 , 2 ] Cases of elderly patients with progressive language deterioration have been described since Arnold Pick's landmark case report of 1892. (medscape.com)
  • Patients exhibit progressive changes in social, behavioral, and/or language function. (bvsalud.org)
  • Neurodegeneration in patients with Primary Progressive Aphasia (PPA) decreases local blood flow affecting both language and domain-general performance. (easychair.org)
  • Our objective was to determine whether the atrophic posterior IFC is differentially recruited for the processing of syntactically complex sentences in nonfluent PPA. (unitn.it)
  • There is a third form of primary progressive aphasia (PPA) called logopenic variant primary progressive aphasia (lvPPA). (ucsf.edu)
  • We use the overall umbrella term of FTD, there are two types: there is a behavioural variant and primary progressive aphasia. (rarerevolutionmagazine.com)
  • Non-verbal auditory impairment is increasingly recognised in the primary progressive aphasias (PPAs) but its relationship to speech processing and brain substrates has not been defined. (biomedcentral.com)
  • She was originally diagnosed with the FTD subtype, progressive nonfluent aphasia. (alzforum.org)
  • Some members may present primarily with amyotrophy, and others may present with primary supranuclear gaze palsy, parkinsonism, schizophrenialike thought disorder, or progressive aphasia and/or apraxia. (medscape.com)
  • This disorder commonly has a primary effect on the left hemisphere, causing the symptomatic display of expressive language deficits (production difficulties) and sometimes may disrupt receptive abilities in comprehending grammatically complex language. (wikipedia.org)
  • Studies have documented the benefits of script training for functional communication in aphasia, but few have examined whether script training can remediate underlying linguistic deficits. (easychair.org)
  • [ 3 ] As Pick stated, "simple progressive brain atrophy can lead to symptoms of local disturbance through local accentuation of the diffuse process. (medscape.com)
  • We examined the effects of script training with embedded syntactic targets on the ability of participants with progressive agrammatic aphasia to accurately produce complex syntactic structures in constrained tasks and spontaneous speech. (easychair.org)
  • eg difficulty using or understanding words (aphasia) and difficulty speaking properly (e.g., slurred speech). (bestbulksmsonline.com)
  • Primary progressive aphasia - Known as PPA, this type of FTD degeneration focuses on the loss of language abilities in both the receptive and expressive realms. (mentalhealth.com)
  • 2. Primary progressive aphasia PPA: Changes in the ability to communicate (use of language to speak, read, write, and understand what others are saying). (bestbulksmsonline.com)
  • Progressive supranuclear palsy (PSP), rare neurological movement disorders associated with FTD, may affect thinking and language abilities. (bestbulksmsonline.com)
  • As neurons in these areas stop working, the primary FTD symptoms discussed below begin to appear. (mentalhealth.com)
  • Primary lateral sclerosis Amyotrophic lateral sclerosis and other motor neuron diseases are characterized by steady, relentless, progressive degeneration of corticospinal tracts, anterior horn cells, bulbar motor nuclei. (msdmanuals.com)
  • however, individuals with FTD experience a progressive decline in behaviour and changes in their personality. (rarerevolutionmagazine.com)
  • Fewer Pick bodies may be present in these regions if the primary symptoms are behavioral (behavioral variant), compared with the primary symptoms of aphasia. (medscape.com)
  • Symptoms of progressive supranuclear palsy usually begin in late middle age. (msdmanuals.com)
  • Findings support the utility of implicit modes of training for syntax production in agrammatic progressive aphasia, consistent with evidence of implicit learning and positive effects of implicit priming in treatment for stroke-induced agrammatic aphasia. (easychair.org)
  • however, the functional status of this region in nonfluent PPA is not well understood. (unitn.it)
  • His Social cognition study which covers Empathy that intersects with Primary progressive aphasia. (research.com)

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