about
Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.Distal amyotrophy of predominantly the upper limbs with pyramidal features in a large kinship.Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.Palmoplantar keratoderma, nail dystrophy, and hereditary motor and sensory neuropathy: an autosomal dominant trait.Sensory neuropathy in hereditary spastic paraplegia.Peroneal muscular atrophy with pyramidal tract features (hereditary motor and sensory neuropathy type V): a clinical, neurophysiological, and pathological study of a large kindred.Hereditary spastic paraparesis: a review of new developments.Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.Distal hereditary upper limb muscular atrophySpinal muscular atrophy: clinical classification and disease heterogeneity.Central motor conduction in a family with hereditary motor and sensory neuropathy with pyramidal signs (HMSN V)Spastic paraparesis and sensory neuropathy.Autosomal dominant juvenile amyotrophic lateral sclerosis.Central motor pathway evaluation using magnetic coil stimulation in hereditary motor and sensory neuropathy type I (HMSN type I, Charcot-Marie-Tooth disease).NEFL E396K mutation is associated with a novel dominant intermediate Charcot-Marie-Tooth disease phenotype.
P2860
Q24538838-491659A2-9523-4D62-BF29-C8718296BAD4Q33620866-57B4E744-0EF9-42F1-A781-0DFCEFBB6EB1Q33629602-18271EF7-63A7-442A-8B54-B82BDFE0B789Q33682048-936F0705-3479-4C59-840E-018A021EB316Q33732596-2332C584-F78A-4736-A494-21E673EB2EA6Q33733242-DCDB83E6-F0BD-4EE0-BEEE-581F38BA86B7Q33969651-B5329D7D-9EC3-411D-B7B5-75ACEC24DEE5Q35198918-3A6B77AC-8C13-47B3-9C08-23F54D73A596Q36317832-669AECDC-B445-4D2C-9742-8BA79EB0239EQ36924707-880A1F25-5FCD-4F68-8864-8517FC15F234Q36948759-4EA317D7-B27D-4ED8-9566-C484412607A5Q39517121-CD7CC482-297E-479E-AAD9-C5F1FC3DC609Q48147320-94BC214E-6209-4E39-A21C-3DB3FE375FEBQ48498360-D6AB79CC-E08F-4642-B9C8-5B4092BF74DCQ50448017-303B1850-9A70-490D-8777-BC9B1620F638
P2860
description
1984 nî lūn-bûn
@nan
1984 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
1984 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
name
Peroneal muscular atrophy with pyramidal features
@ast
Peroneal muscular atrophy with pyramidal features
@en
type
label
Peroneal muscular atrophy with pyramidal features
@ast
Peroneal muscular atrophy with pyramidal features
@en
prefLabel
Peroneal muscular atrophy with pyramidal features
@ast
Peroneal muscular atrophy with pyramidal features
@en
P2860
P356
P1476
Peroneal muscular atrophy with pyramidal features
@en
P2093
P2860
P304
P356
10.1136/JNNP.47.2.168
P407
P577
1984-02-01T00:00:00Z