Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease. - Wikidata - awgldk - TriplyDB

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

http://www.wikidata.org/entity/Q33828930

about

Hirayama's disease: an Italian single center experience and review of the literature Targeting Glioma with a Dual Mode Optical and Paramagnetic Nanoprobe across the Blood-brain Tumor Barrier Cervical spine MR imaging findings of patients with Hirayama disease in North America: a multisite study.

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P2860

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

http://www.wikidata.org/entity/Q33828930

description

2010 nî lūn-bûn

@nan

2010 թուականի Յունուարին հրատարակուած գիտական յօդուած

@hyw

2010 թվականի հունվարին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

@zh-hk

2010年論文

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2010年論文

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2010年论文

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name

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

@ast

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

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type

label

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

@ast

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

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prefLabel

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

@ast

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

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Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders

P1476

Mutational analysis of glycyl-tRNA synthetase (GARS) gene in Hirayama disease.

@en

P2093

Baruch El-Ad

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Galina B Groozman

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Lev G Goldfarb

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Menachem Sadeh

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Sergiu C Blumen

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Uri Soimu

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Vivian E Drory

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P2860

Non familial juvenile distal spinal muscular atrophy of upper extremity

Juvenile muscular atrophy of distal upper extremity (Hirayama disease).

Phenotypic spectrum of disorders associated with glycyl-tRNA synthetase mutations.

The G526R glycyl-tRNA synthetase gene mutation in distal hereditary motor neuropathy type V.

Long-term follow-up of 44 patients with brachial monomelic amyotrophy.

A clinical, magnetic resonance imaging, and survival motor neuron gene deletion study of Hirayama disease.

Familial Juvenile Focal Amyotrophy of the Upper Extremity (Hirayama Disease)

Morphological changes of the lower cervical spinal cord under neutral and fully flexed position by MRI in Chinese patients with Hirayama's disease

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237-239

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scholarly article

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10.3109/17482960902849823

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1-2

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11

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Jean-Pierre Bouchard

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2010-01-01T00:00:00Z

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24399190

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19412816

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