Results 191 to 200 of about 2,449,997 (351)

The Diverse Neuromuscular Spectrum of VPS13A Disease

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective VPS13A disease (chorea‐acanthocytosis) is a rare neurodegenerative disorder caused by biallelic variants in VPS13A, typically presenting with hyperkinetic movement disorders, while neuromuscular signs are often mild. The aim of the project was to investigate the frequency and severity of neuromuscular impairment in VPS13A disease ...
Anne Buchberger   +16 more
wiley   +1 more source

Agreement Between a Wireless Sleeve and a Goniometer in Measuring Elbow and Knee Range of Motion. [PDF]

open access: yesCureus
Neufeld EV   +6 more
europepmc   +1 more source

Active range of motion of the head and cervical spine: a three‐dimensional investigation in healthy young adults [PDF]

open access: bronze, 2002
Virgilio F. Ferrario   +4 more
openalex   +1 more source

Purkinje Cell Loss in Essential Tremor: Collective Data From 215 Brains Over a 21‐Year Period

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Essential tremor is a highly prevalent movement disorder. Pathological changes observed in essential tremor cerebella center around Purkinje cells and neighboring neuronal populations. Postmortem studies have variably, but not always, shown reduced Purkinje cell counts in essential tremor compared to controls.
Chloë A. Kerridge   +4 more
wiley   +1 more source

Metamorphic Flexure Bearings for Extended Range of Motion. [PDF]

open access: yesJ Mech Des N Y
Taylor CR   +5 more
europepmc   +1 more source

Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Hereditary spastic paraplegias (HSP) are rare neurodegenerative disorders marked by spasticity and lower limb weakness. The most common type, SPG4, is usually autosomal dominant and caused by SPAST gene variants, typically presenting as pure HSP.
Gregorio A. Nolasco   +18 more
wiley   +1 more source

The Reliability and Validity of an Instrumented Device for Tracking the Shoulder Range of Motion. [PDF]

open access: yesSensors (Basel)
Roos RE   +18 more
europepmc   +1 more source

Tender Point Sensitivity, Range of Motion, and Perceived Disability in Subjects With Neck Pain

open access: bronze, 2000
S L Olson   +4 more
openalex   +1 more source

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