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Muscle & Nerve. Supplement|January 1, 1995
Characterization of a tandemly repeated 3.3-kb KpnI unit in the facioscapulohumeral muscular dystrophy (FSHD) gene region on chromosome 4q35J H Lee, K Goto, C Matsuda, et al.Muscle & Nerve. Supplement|January 1, 1995
Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4qK D Mathews, K A Mills, H L Bailey, et al.Muscle & Nerve. Supplement|July 13, 2002
Early struggles with single-fiber electromyographyJan E EkstedtMuscle & Nerve. Supplement|July 13, 2002
Safety margin at single neuromuscular junctionsJoze V Trontelj, Marjan Mihelin, Adnan KhuraibetMuscle & Nerve. Supplement|January 1, 1995
Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomasN G Larsson, M H Tulinius, E Holme, et al.Muscle & Nerve. Supplement|January 1, 1995
Clinical features of MELAS and mitochondrial DNA mutationsY GotoMuscle & Nerve. Supplement|January 1, 1995
Mitochondrial diabetes mellitus--glucose-induced signaling defects and beta-cell lossY Oka, H Katagiri, H Ishihara, et al.Muscle & Nerve. Supplement|January 1, 1995
A new mitochondrial DNA deletion associated with diabetic amyotrophy, diabetic myoatrophy and diabetic fatty liverY Hinokio, S Suzuki, K Komatu, et al.Muscle & Nerve. Supplement|January 1, 1995
Duplications of mitochondrial DNA in Kearns-Sayre syndromeJ Poulton, K J Morten, D Marchington, et al.Pageof 11