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Neuromuscular Disorders : NMD|January 1, 1995
Exclusion of the candidate locus FSP1 in six families with late-onset autosomal dominant spastic paraplegiaB Fontaine, C S Rime, J Hazan, et al.Neuromuscular Disorders : NMD|January 1, 1995
Diabetic muscle infarction: a new perspective on pathogenesis and managementE K Bjornskov, M R Carry, F H Katz, et al.Neuromuscular Disorders : NMD|January 1, 1995
Experimental thyrotoxic myopathy: radioautography of protein synthesis in skeletal muscle and motor neurons of spinal cordV M Kazakov, T M KovalenkoNeuromuscular Disorders : NMD|January 1, 1995
Malignant hyperthermia in a patient with Becker muscular dystrophy: dystrophin analysis and caffeine contracture studyN Ohkoshi, T Yoshizawa, H Mizusawa, et al.Neuromuscular Disorders : NMD|September 1, 1994
The gene for X-linked myotubular myopathy is located in an 8 Mb region at the border of Xq27.3 and Xq28E A Janssen, G W Hensels, B A van Oost, et al.Neuromuscular Disorders : NMD|September 1, 1994
Development of a microsatellite genetic map spanning 5q31-q33 and subsequent placement of the LGMD1A locus between D5S178 and IL9L H Yamaoka, C A Westbrook, M C Speer, et al.Neuromuscular Disorders : NMD|September 1, 1994
The natural history of type I (severe) spinal muscular atrophyN H Thomas, V DubowitzNeuromuscular Disorders : NMD|December 5, 2023
Acetaminophen treatment in children and adults with spinal muscular atrophy: a lower tolerance and higher risk of hepatotoxicityMarie Mostue Naume, Qiaolin Zhao, Sissel Sundell Haslund-Krog, et al.Neuromuscular Disorders : NMD|November 23, 2023
Functional characterization of RYR1 variants identified in malignant hyperthermia susceptible individualsYuko Noda, Hirotsugu Miyoshi, Sofia Benucci, et al.Neuromuscular Disorders : NMD|January 17, 2024
Crossover randomized controlled trial of bumetanide to rescue an attack of exercise induced hand weakness in hypokalaemic periodic paralysisRenata Siciliani Scalco, Jasper M Morrow, Andreea Manole, et al.Pageof 341