Results 61 to 70 of about 4,302 (188)

Spectrum of MND registered in Peking Union Medical College Hospital (n = 143). [PDF]

open access: yes, 2015
ALS, amyotrophic lateral sclerosis; MND, motor neuron disease; PBP, progressive bulbar palsy; PLS, progressive lateral sclerosis; PMA, progressive muscular atrophy.
Mingsheng Liu (749595)   +6 more
core   +1 more source

Case Report: Guillain-Barré syndrome mimicking acute brainstem stroke with severe autonomic dysfunction-complete recovery after early plasma exchange

open access: yesFrontiers in Physiology
Acute onset of bilateral ptosis, bulbar palsy, and quadriparesis typically raises suspicion for brainstem infarction. However, when neuroimaging is unrevealing, immune-mediated neuropathies such as Guillain-Barré syndrome (GBS) should be considered. This
Jianming Zhu   +9 more
doaj   +1 more source

AGRN‐, LRP4‐, MUSK‐Related CMS: Clinical, Neurophysiological, Morphological, Genetic and Pathological Mechanisms

open access: yesMuscle &Nerve, EarlyView.
ABSTRACT Congenital myasthenic syndromes (CMS) are inherited disorders caused by mutations in genes encoding proteins essential for neuromuscular junction (NMJ) function. Pathogenic variants have been identified in more than 35 genes, underscoring the complexity of synaptic biology and the wide range of mechanisms that can compromise neuromuscular ...
Rocio‐Nur Villar‐Quiles   +5 more
wiley   +1 more source

Carcinoma of the tongue and bulbar-onset amyotrophic lateral sclerosis: unusual differential diagnosis. [PDF]

open access: yes, 2007
We present a 72-year-old woman with progressive dysphagia, dysarthria and tongue palsy who was initially diagnosed with bulbar-onset amyotrophic lateral sclerosis (ALS).
VOLANTI P   +3 more
core   +1 more source

Utilizing speech analysis to differentiate progressive supranuclear palsy from Parkinson's disease [PDF]

open access: yes, 2023
Introduction: Distinguishing Parkinson\u27s disease (PD) from Progressive supranuclear palsy (PSP) at early disease stages is important for clinical trial enrollment and clinical care/prognostication. Methods: We recruited 21 participants with PSP(n = 11)
Bijan Najafi   +25 more
core   +1 more source

Progressive Supranuclear Palsy (PSP):An Atypical Case [PDF]

open access: yes, 2023
Progressive Supranuclear Palsy (PSP), also known as Steele-Richardson-Olszewski syndrome, is recognized as one of the most common extrapyramidal neurodegenerative disorders, following in prevalence after Parkinson's disease.
Zafirov, Stojance   +3 more
core  

Incidence of unplanned gastrostomy tube replacements and associated complications in people with motor neurone disease and other conditions: A retrospective audit of an Australian dietitian‐led clinic

open access: yesNutrition in Clinical Practice, EarlyView.
Abstract Background Gastrostomy tube placement is a common intervention for long‐term nutrition in people with dysphagia. Minimising complications such as tube dislodgement is integral in gastrostomy management, as unplanned replacements may require urgent care to prevent stoma closure.
Emily Farrugia   +6 more
wiley   +1 more source

Identifying Novel Modifiable Risk Factors in Progressive Supranuclear Palsy (PSP): A Secondary Use Analysis of Clinical Trial Data [PDF]

open access: yes, 2023
Much of the current research efforts to treat neurological diseases have been focused on identifying novel disease biomarkers to aid in diagnosis, provide prognostic information, and monitor disease progression.
Sharma, Mansi
core  

Oral Health Care Services, Barriers and Enablers to Maintaining Good Oral Health in Motor Neurone Disease: A Scoping Review

open access: yesCommunity Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Objectives The objective of this scoping review was to map existing literature on oral health and related care in individuals with Motor Neurone Disease (MND). Specifically, the review aimed to identify barriers and facilitators to maintaining oral hygiene, summarise available clinical guidelines and patient‐facing resources, and examine how ...
Mariam A. Khokhar   +3 more
wiley   +1 more source

Expanding Spectrum of FIG4‐Related Neurological Disorders of Lysosomal Homeostasis: Case Report and Overview of the Potential Genotype–Phenotype Correlations

open access: yesClinical Genetics, EarlyView.
FIG4 is essential for lysosomal homeostasis. FIG4‐related disorders present as a continuous spectrum from the juvenile lethality in Yunis‐Varon syndrome to an increased risk of amyotrophic lateral sclerosis (ALS) in adult life. FIG4‐related disorders comprise a novel group of disorders of lysosomal homeostasis and can be classified into severe ...
Pankaj Prasun, Matthew Rasberry
wiley   +1 more source

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