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Journal of the Neurological Sciences|September 1, 1987
Benign juvenile focal muscular atrophy of upper extremities--a familial caseU Schlegel, F Jerusalem, W Tackmann, et al.
Neuromuscular Disorders : NMD|July 17, 1999
Mitochondrial 3243 A-->G mutation (MELAS mutation) associated with painful muscle stiffnessM Deschauer, T Wieser, S Neudecker, et al.
Biological Chemistry Hoppe-Seyler|August 1, 1985
Glucostat capacity and metabolic zonation in rat liver after portocaval anastomosisB Wittig, S Zierz, G Gubernatis, et al.
Deutsche Medizinische Wochenschrift (1946)|April 4, 1980
[Carnitine deficiency myopathy (author's transl)]F Jerusalem, A G Engel, C Sengupta, et al.
Molecular Genetics and Metabolism|August 5, 2000
Higher proportion of mitochondrial A3243G mutation in blood than in skeletal muscle in a patient with cardiomyopathy and hearing lossM Deschauer, S Neudecker, T Müller, et al.
Neurology|January 26, 2005
Sensory ataxic neuropathy due to a novel C10Orf2 mutation with probable germline mosaicismG Hudson, M Deschauer, K Busse, et al.
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