Results 131 to 140 of about 120,926 (203)

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  

Peroneal neuropathy with foot drop after bariatric surgery: A neurosurgical perspective. [PDF]

open access: yesDusunen Adam
Gunduz HB   +6 more
europepmc   +1 more source

Talus Bipartitus: A Rare Anatomical Variant Presenting as an Entrapment Neuropathy of the Tibial Nerve within the Tarsal Tunnel. [PDF]

open access: yesCase Rep Orthop, 2018
Abrego MO   +6 more
europepmc   +1 more source

Dorsal scapular nerve entrapment: a systematic review. [PDF]

open access: yesJSES Rev Rep Tech
Afshar A, Tabrizi A, Shariyate MJ.
europepmc   +1 more source

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