Double trouble: Spinal muscular atrophy type II and seropositive myasthenia gravis in the same patient
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference8 articles.
1. Spinal muscular atrophies;Rudnik-Schöneborn,2004
2. Spinal muscular atrophy: survival pattern and functional status;Chung;Pediatrics,2004
3. X-linked spinal and bulbar muscular atrophy with myasthenic symptoms;Yamada;J Neurol Sci,1997
4. Ocular myasthenia gravis associated with x-linked recessive spinal and bulbar muscular atrophy;Boz;J Clin Neuromuscul Dis,2004
5. Amyotrophic lateral sclerosis with anti-acetylcholine receptor antibody;Okuyama;Intern Med,1997
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Double trouble: A case of spinal muscular atrophy type III found to be complicated by myasthenia gravis due to subacute dysphagia;Clinical and Experimental Neuroimmunology;2022-06-10
2. Neurofibromatosis type 1 (NF1) with an unusually severe phenotype due to digeny for NF1 and ryanodine receptor 1 associated myopathy;European Journal of Pediatrics;2014-04-08
3. Myasthenic symptoms in a patient with Kennedy’s disease;Acta Neurologica Belgica;2013-02-27
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