Muscle magnetic resonance imaging in congenital myasthenic syndromes. - Wikidata - awgldk - TriplyDB

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

http://www.wikidata.org/entity/Q37169452

about

Design and test of a double-nuclear RF coil for (1)H MRI and (13)C MRSI at 7T.Clinical features of the myasthenic syndrome arising from mutations in GMPPB.Congenital Myasthenic Syndrome due to DOK7 mutations in a family from Chile.

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Muscle magnetic resonance imaging in congenital myasthenic syndromes.

http://www.wikidata.org/entity/Q37169452

description

article científic

@ca

article scientifique

@fr

articolo scientifico

@it

artigo científico

@pt

bilimsel makale

@tr

scientific article published on 20 January 2016

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@en

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@nl

type

label

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@en

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@nl

prefLabel

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@en

Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@nl

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Muscle and Nerve

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Muscle magnetic resonance imaging in congenital myasthenic syndromes.

@en

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Arne Fischmann

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Christopher D J Sinclair

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David Beeson

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Jasper M Morrow

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John S Thornton

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Mel White

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Michal Al-Hajjar

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Nicola Carboni

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Pedro M Rodriguez Cruz

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Sandeep Jayawant

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P2860

Approach to the diagnosis of congenital myopathies

Congenital myasthenic syndromes due to mutations in ALG2 and ALG14.

DPAGT1 myasthenia and myopathy: genetic, phenotypic, and expression studies.

Upper girdle imaging in facioscapulohumeral muscular dystrophy.

Myasthenia gravis: recommendations for clinical research standards. Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America.

Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7

Neuromuscular imaging in inherited muscle diseases

Congenital myasthenic syndromes in 2012.

Mutations in DPAGT1 cause a limb-girdle congenital myasthenic syndrome with tubular aggregates.

The use of MRI in the evaluation of myopathy.

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211-219

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scholarly article

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10.1002/MUS.25035

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2

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54

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Jacqueline Palace

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2016-01-20T00:00:00Z

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