Showing results (501-510 of 3,396) with videos related to

Sort By:
Pageof 340
Neuromuscular Disorders : NMD|August 30, 2020
A family with adult-onset myofibrillar myopathy with BAG3 mutation (P470S) presenting with axonal polyneuropathyMai Hamaguchi, Norito Kokubun, Michio Inoue, et al.
Neuromuscular Disorders : NMD|December 27, 2017
Early-onset axonal Charcot-Marie-Tooth disease due to SACS mutationPaulo Victor Sgobbi Souza, Thiago Bortholin, Fernando George Monteiro Naylor, et al.
Neuromuscular Disorders : NMD|October 4, 2005
A and B utrophin in human muscle and sarcolemmal A-utrophin associated with tumoursC A Sewry, K J Nowak, J T Ehmsen, et al.
Neuromuscular Disorders : NMD|October 4, 2005
IBM-type inclusions in a patient with slow-channel syndrome caused by a mutation in the AChR epsilon subunitAnna Fidzianska, B Ryniewicz, Xing-Ming Shen, et al.
Neuromuscular Disorders : NMD|October 4, 2005
Increased muscle nucleoside levels associated with a novel frameshift mutation in the thymidine phosphorylase gene in a Spanish patient with MNGIEA Blazquez, M A Martín, M C Lara, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Is selection required for the accumulation of somatic mitochondrial DNA mutations in post-mitotic cells?S E Durham, D C Samuels, P F Chinnery
Neuromuscular Disorders : NMD|May 17, 2006
POMT2 mutation in a patient with 'MEB-like' phenotypeE Mercuri, A D'Amico, A Tessa, et al.
Neuromuscular Disorders : NMD|May 11, 2006
Novel slow-skeletal myosin (MYH7) mutation in the original myosin storage myopathy kindredDanielle E Dye, Biagio Azzarelli, Hans H Goebel, et al.
Neuromuscular Disorders : NMD|March 21, 2006
Long-term benefits of deflazacort treatment for boys with Duchenne muscular dystrophy in their second decadeW D Biggar, V A Harris, L Eliasoph, et al.
Neuromuscular Disorders : NMD|April 20, 2006
Predictors of severe chest infections in pediatric neuromuscular disordersC Dohna-Schwake, R Ragette, H Teschler, et al.
Pageof 340