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Neuromuscular Disorders : NMD|July 26, 2020
SMALED2 with BICD2 gene mutations: Report of two cases and portrayal of a classical phenotypeVincent Picher-Martel, Clément Morin, Denis Brunet, et al.
Neuromuscular Disorders : NMD|January 25, 2015
Targeted sequencing and identification of genetic variants in sporadic inclusion body myositisConrad C Weihl, Robert H Baloh, Youjin Lee, et al.
Neuromuscular Disorders : NMD|February 2, 2015
Mitochondrial pathology in inclusion body myositisUlrika Lindgren, Sara Roos, Carola Hedberg Oldfors, et al.
Neuromuscular Disorders : NMD|October 16, 2012
Presymptomatic late-onset Pompe disease identified by the dried blood spot testMatias Wagner, Amina Chaouch, Juliane S Müller, et al.
Neuromuscular Disorders : NMD|February 10, 2015
SCN4A mutation as modifying factor of myotonic dystrophy type 2 phenotypeE Bugiardini, I Rivolta, A Binda, et al.
Neuromuscular Disorders : NMD|January 31, 2015
Studying the role of dystrophin-associated proteins in influencing Becker muscular dystrophy disease severityJ C van den Bergen, B H A Wokke, M A Hulsker, et al.
Neuromuscular Disorders : NMD|July 25, 2012
Brown-Vialetto-van Laere and Fazio-Londe overlap syndromes: a clinical, biochemical and genetic studyMarianna Ciccolella, Michela Catteruccia, Sabina Benedetti, et al.
Neuromuscular Disorders : NMD|April 27, 2021
Ranolazine-induced lipid storage myopathy presenting with respiratory failure and head dropPritikanta Paul, Rocio Vazquez Do Campo, Teerin Liewluck, et al.
Neuromuscular Disorders : NMD|May 20, 2023
Expanding the phenotype of DNMT3A as a cause a congenital myopathy with rhabdomyolysisRoula Ghaoui, Thuong T Ha, Jennifer Kerkhof, et al.
Neuromuscular Disorders : NMD|May 17, 2023
Limitations of the apnea-hypopnea index in children and young adults with neuromuscular disordersLucia Ronco, Sonia Khirani, Meryl Vedrenne-Cloquet, et al.
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