Diagnose und Therapie der kongenitalen Myastheniesyndrome-Reference-Cited by-同舟云学术

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Diagnose und Therapie der kongenitalen Myastheniesyndrome

Published:2005-05 Issue:5 Volume:153 Page:453-462
ISSN:0026-9298
Container-title:Monatsschrift Kinderheilkunde
language:de
Short-container-title:Monatsschr Kinderheilkd

Author:

Sieb J. P.,Hans M.,Swandulla D.,Marquard K.,Steinlein O. K.

Publisher

Springer Science and Business Media LLC

Subject

Surgery,Pediatrics, Perinatology and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00112-003-0874-z.pdf

Reference39 articles.

1. AAEM Quality Assurance Commitee (2001) Literature review of the usefulness of repetitive nerve stimulation and single fiber EMG in the electrodiagnostic evaluation of patients with suspected myasthenia gravis or Lambert-Eaton myasthenic syndrome. Muscle Nerve 24:1239–1247

2. AAEM Quality Assurance Commitee (2001) Practice parameter for repetitive nerve stimulation and single fiber EMG evaluation of adults with suspected myasthenia gravis or Lambert-Eaton myasthenic syndrome: summary statement. Muscle Nerve 24:1236–1238

3. Abicht A, Stucka R, Karcagi V et al. (1999) A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin. Neurology 53:1564–1569

4. Bergoffen J, Zmijewski CM, Fischbeck KH (1994) Familial autoimmune myasthenia gravis. Neurology 44:551–554

5. Brownlow S, Webster R, Croxen R et al. (2001) Acetylcholine receptor δ subunit mutations underlie a fast-channel myasthenic syndrome and arthrogryposis multiplex congenita. J Clin Invest 108:125–130

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1. Erworbene Erkrankungen der peripheren Nerven und der Muskulatur;Therapie der Krankheiten im Kindes- und Jugendalter

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