Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.
about
PMP22 exon 4 deletion causes ER retention of PMP22 and a gain-of-function allele in CMT1E.Hereditary neuropathy with liability to pressure palsy (HNPP): report of a family with a new point mutation in PMP22 gene.Pain in hereditary neuropathy with liability to pressure palsy: an association with fibromyalgia syndrome?Effect of low frequency transcutaneous magnetic stimulation on sensory and motor transmission.Characterisation of pain in people with hereditary neuropathy with liability to pressure palsy.
P2860
Clinical, electrophysiological and magnetic resonance findings in a family with hereditary neuropathy with liability to pressure palsies caused by a novel PMP22 mutation.
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh
2013年學術文章
@zh-hant
name
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@en
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@nl
type
label
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@en
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@nl
prefLabel
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@en
Clinical, electrophysiological ...... sed by a novel PMP22 mutation.
@nl
P50
P1476
Clinical, electrophysiological ...... used by a novel PMP22 mutation
@en
P2093
Izaskun Yurrebaso
Oscar L Casado
P356
10.1016/J.NMD.2013.09.005
P577
2013-09-13T00:00:00Z