Literature DB >> 21498094

Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes.

Nina Barišić1, Amina Chaouch, Juliane S Müller, Hanns Lochmüller.   

Abstract

Congenital myasthenic syndromes (CMS) are a rare heterogeneous group of inherited neuromuscular disorders associated with distinctive clinical, electrophysiological, ultrastructural and genetic abnormalities. These genetic defects either impair neuromuscular transmission directly or result in secondary impairments, which eventually compromise the safety margin of neuromuscular transmission. In this report we will explore the significant progress made in understanding the molecular pathogenesis of CMS, which is important for both patients and clinicians in terms of reaching a definite diagnosis and selecting the most appropriate treatment.
Copyright © 2011 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 21498094     DOI: 10.1016/j.ejpn.2011.03.006

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  8 in total

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Review 2.  Ephedrine for myasthenia gravis, neonatal myasthenia and the congenital myasthenic syndromes.

Authors:  Charlotte Vrinten; Angeli M van der Zwaag; Stephanie S Weinreich; Rob J P M Scholten; Jan J G M Verschuuren
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3.  Congenital myasthenic syndromes in adult neurology clinic: A long road to diagnosis and therapy.

Authors:  Justin C Kao; Margherita Milone; Duygu Selcen; Xin-Ming Shen; Andrew G Engel; Teerin Liewluck
Journal:  Neurology       Date:  2018-10-05       Impact factor: 9.910

4.  Defective presynaptic choline transport underlies hereditary motor neuropathy.

Authors:  Katy E S Barwick; Jane Wright; Saeed Al-Turki; Meriel M McEntagart; Ajith Nair; Barry Chioza; Ali Al-Memar; Hamid Modarres; Mary M Reilly; Katherine J Dick; Alicia M Ruggiero; Randy D Blakely; Matt E Hurles; Andrew H Crosby
Journal:  Am J Hum Genet       Date:  2012-11-08       Impact factor: 11.025

Review 5.  Neuromuscular disorders in zebrafish: state of the art and future perspectives.

Authors:  Andrea Pappalardo; Letizia Pitto; Chiara Fiorillo; M Alice Donati; Claudio Bruno; Filippo M Santorelli
Journal:  Neuromolecular Med       Date:  2013-04-13       Impact factor: 3.843

6.  Mutations in the Mitochondrial Citrate Carrier SLC25A1 are Associated with Impaired Neuromuscular Transmission.

Authors:  Amina Chaouch; Vito Porcelli; Daniel Cox; Shimon Edvardson; Pasquale Scarcia; Anna De Grassi; Ciro L Pierri; Judith Cossins; Steven H Laval; Helen Griffin; Juliane S Müller; Teresinha Evangelista; Ana Töpf; Angela Abicht; Angela Huebner; Maja von der Hagen; Kate Bushby; Volker Straub; Rita Horvath; Orly Elpeleg; Jacqueline Palace; Jan Senderek; David Beeson; Luigi Palmieri; Hanns Lochmüller
Journal:  J Neuromuscul Dis       Date:  2014

Review 7.  Genetic neurological channelopathies: molecular genetics and clinical phenotypes.

Authors:  J Spillane; D M Kullmann; M G Hanna
Journal:  J Neurol Neurosurg Psychiatry       Date:  2015-11-11       Impact factor: 10.154

8.  Truncating SLC5A7 mutations underlie a spectrum of dominant hereditary motor neuropathies.

Authors:  Claire G Salter; Danique Beijer; Holly Hardy; Katy E S Barwick; Matthew Bower; Ines Mademan; Peter De Jonghe; Tine Deconinck; Mark A Russell; Meriel M McEntagart; Barry A Chioza; Randy D Blakely; John K Chilton; Jan De Bleecker; Jonathan Baets; Emma L Baple; David Walk; Andrew H Crosby
Journal:  Neurol Genet       Date:  2018-03-23
  8 in total

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