标题
Therapeutic strategies for congenital myasthenic syndromes
作者
关键词
-
出版物
Annals of the New York Academy of Sciences
Volume 1412, Issue 1, Pages 129-136
出版商
Wiley
发表日期
2018-01-31
DOI
10.1111/nyas.13538
参考文献
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注意:仅列出部分参考文献,下载原文获取全部文献信息。- Congenital myasthenic syndromes
- (2016) David Beeson CURRENT OPINION IN NEUROLOGY
- Clinical features of the myasthenic syndrome arising from mutations in GMPPB
- (2016) Pedro M Rodríguez Cruz et al. JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY
- Antidepressant Use Late in Pregnancy and Risk of Persistent Pulmonary Hypertension of the Newborn
- (2015) Krista F. Huybrechts et al. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION
- Editorial by concerned physicians: Unintended effect of the orphan drug act on the potential cost of 3,4-diaminopyridine
- (2015) Ted M. Burns et al. MUSCLE & NERVE
- Salbutamol and ephedrine in the treatment of severe AChR deficiency syndromes
- (2015) Pedro M. Rodríguez Cruz et al. NEUROLOGY
- Impaired Synaptic Development, Maintenance, and Neuromuscular Transmission in LRP4-Related Myasthenia
- (2015) Duygu Selcen et al. JAMA Neurology
- Congenital myasthenic syndromes due to mutations inALG2andALG14
- (2013) Judith Cossins et al. BRAIN
- Salbutamol-responsive limb-girdle congenital myasthenic syndrome due to a novel missense mutation and heteroallelic deletion in MUSK
- (2013) Constanze Gallenmüller et al. NEUROMUSCULAR DISORDERS
- Mutations in DPAGT1 Cause a Limb-Girdle Congenital Myasthenic Syndrome with Tubular Aggregates
- (2012) Katsiaryna Belaya et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Pregnancy in congenital myasthenic syndrome
- (2012) L. Servais et al. JOURNAL OF NEUROLOGY
- Vertebrate protein glycosylation: diversity, synthesis and function
- (2012) Kelley W. Moremen et al. NATURE REVIEWS MOLECULAR CELL BIOLOGY
- Salbutamol benefits children with congenital myasthenic syndrome due to DOK7 mutations
- (2012) Georgina Burke et al. NEUROMUSCULAR DISORDERS
- Neuromuscular Junction Acetylcholinesterase Deficiency Responsive to Albuterol
- (2012) Sophelia H.S. Chan et al. PEDIATRIC NEUROLOGY
- A retrospective clinical study of the treatment of slow-channel congenital myasthenic syndrome
- (2011) Amina Chaouch et al. JOURNAL OF NEUROLOGY
- Congenital myasthenic syndrome with tubular aggregates caused by GFPT1 mutations
- (2011) Velina Guergueltcheva et al. JOURNAL OF NEUROLOGY
- Beneficial effects of albuterol in congenital endplate acetylcholinesterase deficiency and Dok-7 myasthenia
- (2011) Teerin Liewluck et al. MUSCLE & NERVE
- Clinical features in a series of fast channel congenital myasthenia syndrome
- (2011) Jacqueline Palace et al. NEUROMUSCULAR DISORDERS
- Mutations in MUSK causing congenital myasthenic syndrome impair MuSK–Dok-7 interaction
- (2010) Ricardo A. Maselli et al. HUMAN MOLECULAR GENETICS
- Ephedrine treatment in congenital myasthenic syndrome due to mutations in DOK7
- (2010) D. Lashley et al. NEUROLOGY
- Identification of an Agrin Mutation that Causes Congenital Myasthenia and Affects Synapse Function
- (2009) Caroline Huzé et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Ephedrine therapy in eight patients with congenital myasthenic syndrome due to DOK7 mutations
- (2009) U. Schara et al. NEUROMUSCULAR DISORDERS
- The congenital myasthenic syndromes
- (2008) Jackie Palace et al. JOURNAL OF NEUROIMMUNOLOGY
- Transient neonatal Lambert-Eaton syndrome
- (2008) U. Reuner et al. JOURNAL OF NEUROLOGY
- Therapeutic strategies in congenital myasthenic syndromes
- (2008) Ulrike Schara et al. Neurotherapeutics
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