Showing results (111-120 of 185) with videos related to
Sort By:
Pageof 19
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.Der Nervenarzt|December 25, 2012
[Myofibrillary myopathy due to the ZASP mutation Ala147Thr : two cases with exclusively distal leg involvement]T Kraya, W Kress, D Stoevesant, et al.Neurology|April 23, 2003
Carnitine palmitoyltransferase II deficiency: molecular and biochemical analysis of 32 patientsT Wieser, M Deschauer, K Olek, et al.Biological Chemistry Hoppe-Seyler|May 1, 1985
Metabolic zonation in liver of diabetic rats. Zonal distribution of phosphoenolpyruvate carboxykinase, pyruvate kinase, glucose-6-phosphatase and succinate dehydrogenaseH Miethke, B Wittig, A Nath, 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.FEBS Letters|April 26, 1993
Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu(UUR) geneK D Gerbitz, A Paprotta, M Jaksch, 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.Pageof 19