Congenital myasthenic syndrome due to mutation in CHRNE gene with clinical worsening and thymic hyperplasia attributed to association with autoimmune-myasthenia gravis
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health
Reference23 articles.
1. Current status of the congenital myasthenic syndromes;Engel;Neuromuscul Disord,2012
2. Clinical, pathological, HLA antigen and immunological evidence for disease heterogeneity in myasthenia gravis;Compston;Brain,1980
3. Genetic factors in autoimmune myasthenia gravis;Giraud;Ann N Y Acad Sci,2008
4. Recent advances in genetic predisposition of myasthenia gravis;Zagoriti;Biomed Res Int,2013
5. Human muscle acetylcholine receptor alpha-subunit gene (CHRNA1) association with autoimmune myasthenia gravis in black, mixed-ancestry and Caucasian subjects;Heckmann;J Autoimmun,1996
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2. Innovative Therapeutic Approaches in Congenital Myasthenic Syndromes;Neurology Clinical Practice;2024-06
3. Les syndromes myasthéniques congénitaux avec anomalies cinétiques du récepteur à l’acétylcholine;médecine/sciences;2023-11
4. Oculopharyngeal muscular dystrophy coexisting with myasthenia gravis;Practical Neurology;2022-05-09
5. Pharmacological Strategy for Congenital Myasthenic Syndrome with CHRNE Mutations: A Meta-Analysis of Case Reports;Current Neuropharmacology;2021-04-29
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