Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

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Intermediate Charcot-Marie-Tooth disease: an electrophysiological reappraisal and systematic review.

P2860

Q39212369-2267E03E-AC44-4ED1-A4DD-2F0096E9EC32

P2860

Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

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http://www.wikidata.org/entity/Q41004180

description

2016 nî lūn-bûn

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2016年の論文

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2016年論文

@yue

2016年論文

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2016年論文

@zh-hk

2016年論文

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2016年論文

@zh-tw

2016年论文

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2016年论文

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2016年论文

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name

Clinical, neurophysiological a ...... Marie-Tooth type C neuropathy.

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type

Item

label

Clinical, neurophysiological a ...... Marie-Tooth type C neuropathy.

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Clinical, neurophysiological a ...... Marie-Tooth type C neuropathy.

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P1476

Clinical, neurophysiological a ...... Marie-Tooth type C neuropathy.

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P2093

Albena Jordanova

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Boryana Ishpekova

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Chitharanjan V Rao

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Florian P Thomas

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Francisco A A Gondim

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Ivailo Tournev

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Ivan Litvinenko

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Laurence J Kinsella

http://www.w3.org/2001/XMLSchema#string

Peter De Jonghe

http://www.w3.org/2001/XMLSchema#string

Steven S Scherer

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P2860

Glycyl tRNA synthetase mutations in Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V.

Dominant intermediate Charcot-Marie-Tooth type C maps to chromosome 1p34-p35

Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2.

Mutations in the pleckstrin homology domain of dynamin 2 cause dominant intermediate Charcot-Marie-Tooth disease

Disrupted function and axonal distribution of mutant tyrosyl-tRNA synthetase in dominant intermediate Charcot-Marie-Tooth neuropathy

Dominant mutations in the tyrosyl-tRNA synthetase gene recapitulate in Drosophila features of human Charcot-Marie-Tooth neuropathy.

Psychometric evaluation of a new sensory scale in immune-mediated polyneuropathies. Inflammatory Neuropathy Cause and Treatment (INCAT) Group.

A major determinant for binding and aminoacylation of tRNA(Ala) in cytoplasmic Alanyl-tRNA synthetase is mutated in dominant axonal Charcot-Marie-Tooth disease

Compound heterozygosity for loss-of-function lysyl-tRNA synthetase mutations in a patient with peripheral neuropathy.

Lower motor and primary sensory neuron diseases with peroneal muscular atrophy. I. Neurologic, genetic, and electrophysiologic findings in hereditary polyneuropathies.

P2888

s00415-015-7989-8

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467-476

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scholarly article

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10.1007/S00415-015-7989-8

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263

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2016-01-02T00:00:00Z

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289355604

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26725087

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P921

neurophysiology

Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

about

P2860

P2860

Clinical, neurophysiological and morphological study of dominant intermediate Charcot-Marie-Tooth type C neuropathy.

description

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P1433

P1476

P2093

P2860

P2888

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P31

P356

P433

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P5875

P698

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P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P577

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P921