These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
12. Genetic basis and phenotypic features of congenital myasthenic syndromes. Engel AG Handb Clin Neurol; 2018; 148():565-589. PubMed ID: 29478601 [TBL] [Abstract][Full Text] [Related]
18. [Congenital myasthenic syndromes with kinetic abnormalities of the acetylcholine receptor]. Islam Kediha M; Tazir M; Sternberg D; Eymard B; Ali Pacha L Med Sci (Paris); 2023 Nov; 39 Hors série n° 1():58-63. PubMed ID: 37975772 [TBL] [Abstract][Full Text] [Related]
19. Clinical and Genetic Features of Congenital Myasthenic Syndromes due to CHAT Mutations: Case Report and Literature Review. Arican P; Gencpinar P; Cavusoglu D; Olgac Dundar N Neuropediatrics; 2018 Aug; 49(4):283-288. PubMed ID: 29783273 [TBL] [Abstract][Full Text] [Related]
20. Congenital myasthenic syndromes in 2012. Engel AG Curr Neurol Neurosci Rep; 2012 Feb; 12(1):92-101. PubMed ID: 21997714 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]