Literature DB >> 19289485

Novel epsilon subunit mutation of the muscle acetylcholine receptor causing a slow-channel congenital myasthenic syndrome.

O Outteryck, P Richard, A Lacour, E Fournier, H Zéphir, K Gaudon, B Eymard, D Hantaï, P Vermersch, T Stojkovic.   

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Year:  2009        PMID： 19289485     DOI： 10.1136/jnnp.2008.148189

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN： 0022-3050            Impact factor:   10.154


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  3 in total

1.  Pregnancy in congenital myasthenic syndrome.

Authors:  L Servais; H Baudoin; K Zehrouni; P Richard; D Sternberg; E Fournier; B Eymard; T Stojkovic
Journal:  J Neurol       Date:  2012-10-30       Impact factor: 4.849

2.  A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome.

Authors:  Amina Chaouch; Juliane S Müller; Velina Guergueltcheva; Marina Dusl; Ulrike Schara; Vidosava Rakocević-Stojanović; Christopher Lindberg; Rosana H Scola; Lineu C Werneck; Jaume Colomer; Andres Nascimento; Juan J Vilchez; Nuria Muelas; Zohar Argov; Angela Abicht; Hanns Lochmüller
Journal:  J Neurol       Date:  2011-08-07       Impact factor: 4.849

3.  Determinants of the repetitive-CMAP occurrence and therapy efficacy in slow-channel myasthenia.

Authors:  Li Di; Hai Chen; Yan Lu; Duygu Selcen; Andrew G Engel; Yuwei Da; Xin-Ming Shen
Journal:  Neurology       Date:  2020-09-09       Impact factor: 9.910
  3 in total

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