Results 101 to 110 of about 2,123,328 (356)
DIVISION OF MEDIAN NERVE FOLLOWED BY GANGRENE OF FOREFINGER, AND THREATENED GANGRENE OF MIDDLE AND RING FINGER. [PDF]
, 1871 W.A. I'Anson
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Outcome of contralateral C7 nerve transferring to median nerve
Chinese Medical Journal, 2013 Background Contralateral C7 (cC7) transfer had been widely used in many organizations in the world, but the outcomes were significantly different. So the purpose of the study was to evaluate the outcome of patients treated with cC7 transferring to median
Kaiming Gao +3 more
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INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
Annals of Clinical and Translational Neurology, EarlyView.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
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The degenerative changes observed in the structures of the hand, fifteen years after division of the median nerve above the elbow [PDF]
, 1894 Joseph Griffiths
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Expanding Hereditary Spastic Paraplegias Limits: Biallelic SPAST Variants in Cerebral Palsy Mimics
Annals 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
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Case Report: Median Nerve Cavernous Hemangioma
Basic and Clinical Neuroscience, 2017 Hemangiomas of the median nerve are extremely rare; only 12 cases have been reported in the literature. We discuss a patient who presented with paresthesia and pain along the distribution of the left median nerve secondary to a cavernoma of the proximal ...
Mohammed Al-Garnawee, Marwan Najjar
doaj
SUTURE OF SEVERED MEDIAN NERVE, WITH RAPID RECOVERY OF FUNCTION [PDF]
, 1921 Edward D. Wirth
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Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann +6 more
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An unusual case of neuroma of the median nerve. [PDF]
, 1969 R. Kanagasuntheram, Wai‐Choong Wong
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