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Early signs of gait deviation in Duchenne muscular dystrophy. Doglio L, Pavan E, Pernigotti I, Petralia P, Frigo C, Minetti C. Eur J Phys Rehabil Med. 2011 Sep 13. [Epub ahead of...
In a study published in Scientific Reports, an international, multidisciplinary research team that included Binghamton University researchers identified a set of blood proteins tha...
Congenital myopathies are a group of rare, inherited muscle diseases that often cause muscle weakness in childhood. This weakness can affect, among other things, the ability to wal...
A rare congenital muscle disease that robs patients of strength from childhood has long lacked meaningful treatment options, but a new preclinical study offers a striking proof of...
We are thrilled to share that Dr. Sub Subramony, MD, Professor of Neurology at the University of Florida, has been selected by the Muscular Dystrophy Association (MDA) and TREAT-NM...
Musculoskeletal manifestations of Fabry disease: A retrospective study Olivier Lidove et al Joint Bone Spine; 14 December 2015 Objectives Fabry disease is a rare X-...
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