Results 141 to 150 of about 1,542,715 (367)
ABSTRACT Objective To quantify the number and volume of whole brain perivascular spaces (PVS) using a detection and segmentation algorithm in participants with multiple sclerosis (MS) and patients with disorders mimicking MS known to potentially influence PVS, such as cerebrovascular disease.
Elle M. Levit+5 more
wiley +1 more source
Association of clear vs blue-light filtering intraocular lenses with mental and behavioral disorders and diseases of the nervous system among patients receiving bilateral cataract surgery. [PDF]
Karesvuo M+4 more
europepmc +1 more source
THE RELATIONSHIP OF THE SO-CALLED FAMILY DISEASES TO A PREMATURE PHYSIOLOGICAL SENESCENCE LOCALISED TO CERTAIN ORGANIC SYSTEMS, AND CONSIDERED WITH SPECIAL REFERENCE TO THE NERVOUS SYSTEM. [PDF]
F. Lucy Raymond
openalex +1 more source
The Diverse Neuromuscular Spectrum of VPS13A Disease
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
Lettsomian Lectures on Syphilis as a Cause of Disease of the Nervous System [PDF]
W. H. Broadbent
+6 more sources
LESIONS OF THE NERVOUS SYSTEM ETIOLOGICALLY RELATED TO CUTANEOUS DISEASE [PDF]
H. Radcliffe Crocker
openalex +1 more source
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini+7 more
wiley +1 more source
Pregnancy and Autoimmune Disease. [PDF]
Merz WM+4 more
europepmc +1 more source
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano+27 more
wiley +1 more source