[PDF] from distrofiamuscular.netDG Leung, EL Germain-Lee… - Neuromuscular …, 2011 - distrofiamuscular.net ... Muscular Dystrophy Conference December 1–2, 2010, Baltimore, Maryland, USA ... 1. Introduction The Second Endocrine Aspects of Duchenne Muscular Dystrophy Conference convened at the Kennedy Krieger Institute in Baltimore, Maryland, USA from December 1–2, 2010. ... View as HTML
V Raz, S Routledge, A Venema, H Buijze… - The American Journal of …, 2011 - Elsevier Oculopharyngeal muscular dystrophy (OPMD) is an autosomal dominant disease caused by an alanine tract expansion mutation in poly(A)-binding protein nuclear 1 (expPABPN1). To model OPMD in a myogenic and physiological context, we generated mouse myoblast cell ...
AK Ricke, RJ Snook… - Biological psychiatry, 2011 - ncbi.nlm.nih.gov 1. Biol Psychiatry. 2011 Apr 27. [Epub ahead of print] Induction of Prolonged Mania During Ketamine Therapy for Reflex Sympathetic Dystrophy. Ricke AK, Snook RJ, Anand A. Department of Psychiatry, Indiana University, School of Medicine, Indianapolis, Indiana. ... Related articles - All 2 versions
[HTML] from nih.govSA Goonasekera, CK Lam, DP Millay… - The Journal of clinical …, 2011 - ncbi.nlm.nih.gov Muscular dystrophies (MDs) comprise a group of degenerative muscle disorders characterized by progressive muscle wasting and often premature death. The primary defect common to most MDs involves disruption of the dystrophin-glycoprotein complex (DGC). This leads to ... Cited by 1 - Related articles - All 4 versions
G Zachariah, T Idiculla, BR Keshav… - Oman Journal of …, 2011 - ojoonline.org Stargardts macular dystrophy is a genetic disorder with an estimated incidence of 1 in 10,000. It is almost always inherited as an autosomal recessive disorder, with only 10% cases resulting from dominant mode of inheritance. Mutations in Stargardts disease gene ...
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