Results 131 to 140 of about 427,255 (213)

RFC1 Repeat Expansions in Chronic Idiopathic Axonal Polyneuropathy: Prevalence, Phenotype, and Diagnostic Implications. [PDF]

open access: yesJ Peripher Nerv Syst
Gajate-García V   +5 more
europepmc   +1 more source

Amyloid-Like Immunoglobulin Deposition Neuropathy. [PDF]

open access: yesJ Peripher Nerv Syst
Sawaya C   +5 more
europepmc   +1 more source

A study concept of expeditious clinical enrollment for genetic modifier studies in Charcot-Marie-Tooth neuropathy 1A

open access: yes
: BackgroundCaused by duplications of the gene encoding peripheral myelin protein 22 (PMP22), Charcot-Marie-Tooth disease type 1A (CMT1A) is the most common hereditary neuropathy.
Xu, Isaac R.L.   +20 more
core  

Human Disharmony Loop: The Role of the Pectoralis Minor in Thoracic Outlet Syndrome. [PDF]

open access: yesPlast Reconstr Surg Glob Open
Sharma K, Iyengar JJ, Friedman J.
europepmc   +1 more source

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