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Congenital Myasthenic Syndrome due to DOK7 mutations in a family from Chile
2048Downloads: 1320HTML: 232 -
Autophagy increase in Merosin-Deficient Congenital Muscular Dystrophy type 1A
1708Downloads: 651HTML: 20 -
Antibiotic use in endodontic treatment during pregnancy: A narrative review
23706Downloads: 20736HTML: 78 -
History of international connections of myology in Europe
1472Downloads: 355HTML: 13 -
Prevalence of muscular dystrophy in patients with muscular disorders in Tehran, Iran
1416Downloads: 791HTML: 175 -
Compensation for balance disorders: analysis of this multifactorial process
917Downloads: 489HTML: 17 -
44 | Targeted delivery of mir-486 to skeletal muscle: efficacy, tropism, and integrin dependency of MYOAAV2A vs. AAV9 Chiara Ricciardi1, S. Perni1, V. Sorrentino1|2 | 1Department of Molecular and Developmental Medicine, University of Siena, Italy; 2Interdepartmental Program of Molecular Diagnosis and Pathogenetic Mechanisms of Rare Genetic Diseases, Azienda Ospedaliera Universitaria Senese, Italy.
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EJTM3 is also covering Mobility and Medicine at large, an update
1108Downloads: 559HTML: 56 -
31 | Exon skipping peptide-conjugated morpholinos downregulate dynamin 2 to rescue centronuclear myopathy Foteini Moschovaki-Filippidou1, J. de Carvalho Neves1, N. Diedhiou1, Y. Jad2|3, J. Böhm1, M.J.A. Wood2|3, M.A. Varela2|3, J. Laporte1 | 1IGBMC (Institut de Génétique et de Biologie Moléculaire et Cellulaire), Inserm U1258, CNRS UMR7104, Université de Strasbourg, Illkirch, France; 2Department of Paediatrics, Institute of Developmental and Regenerative Medicine (IDRM), University of Oxford, UK; 3MDUK Oxford Neuromuscular Centre, Oxford, UK.
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Novel management of glioma by molecular therapies, a review article
1486Downloads: 789HTML: 38 -
Neuropsychological evaluation of cognitive disorders in children after COVID-19
1943Downloads: 1168HTML: 24
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