Ephedrine for myasthenia gravis, neonatal myasthenia and the congenital myasthenic syndromes

Author:

Vrinten Charlotte1,van der Zwaag Angeli M1,Weinreich Stephanie S1,Scholten Rob JPM2,Verschuuren Jan JGM3

Affiliation:

1. VU University Medical Center; Community Genetics Section, Clinical Genetics; BS7, D450 PO Box 7057 Amsterdam Netherlands 1007 MB

2. Julius Center for Health Sciences and Primary Care / University Medical Center Utrecht; Dutch Cochrane Centre; Room Str. 6.126 P.O. Box 85500 Utrecht Netherlands 3508 GA

3. Leiden University Medical Center; Department of Neurology; PO Box 9600 Leiden Netherlands 2300 RC

Publisher

Wiley

Subject

Pharmacology (medical)

Reference135 articles.

1. Treatment of congenital myasthenia with ephedrine: a case report;Edvardson;European Journal of Paediatric Neurology,2007

2. Abicht A Lochmüller H Congenital Myasthenic Syndromes GeneReviews at Gene Tests: Medical Genetics Information Resource (database online) Seattle University of Washington. Available at www.ncbi.nlm.nih.gov/books/NBK1168/

3. Congenital myasthenia as a cause of respiratory failure in two infants and a toddler: case reports;Adamovičová;Ceska a Slovenska Neurologie a Neurochirurgie,2012

4. Variable phenotypes associated with mutations in DOK7;Anderson;Muscle & Nerve,2008

5. Novel truncating RAPSN mutations causing congenital myasthenic syndrome responsive to 3,4-diaminopyridine;Banwell;Neuromuscular Disorders,2004

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