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Showing results (151-160 of 421) with videos related to

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Journal of the Neurological Sciences|February 1, 1987
Peripheral neuropathy in mitochondrial diseaseG Pezeshkpour, C Krarup, F Buchthal, et al.
Journal of the Neurological Sciences|April 1, 1979
Muscle carnitine deficiency. Genetic heterogeneityJ Willner, S DiMauro, A Eastwood, et al.
Transactions of the American Neurological Association|January 1, 1976
Acid maltase deficiency: reincarnation in cultured muscle fibers of the typical morphological and biochemical defectsV Askanas, W K Engel, S DiMauro, et al.
Annals of Neurology|September 1, 1995
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosisD Thyagarajan, S Shanske, M Vazquez-Memije, et al.
Muscle & Nerve|September 1, 1996
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindredA Toscano, S Tsujino, G Vita, et al.
American Journal of Human Genetics|May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscleC T Moraes, E Ricci, E Bonilla, et al.
Neurologia I Neurochirurgia Polska|January 11, 2002
[Pathomechanism and clinical presentation of neurobehavioral disturbances in a patient with MELAS syndrome]M Pachalska, S DiMauro, B D MacQueen, et al.
The Journal of Clinical Investigation|August 1, 1983
Muscle phosphofructokinase deficiency. Biochemical and immunological studies of phosphofructokinase isozymes in muscle cultureM Davidson, A F Miranda, A N Bender, et al.
Nature|May 25, 1989
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionM Zeviani, S Servidei, C Gellera, et al.
Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, et al.
Pageof 43

Showing results (151-160 of 421) with videos related to

Sort By:
Pageof 43
Journal of the Neurological Sciences|February 1, 1987
Peripheral neuropathy in mitochondrial diseaseG Pezeshkpour, C Krarup, F Buchthal, et al.
Journal of the Neurological Sciences|April 1, 1979
Muscle carnitine deficiency. Genetic heterogeneityJ Willner, S DiMauro, A Eastwood, et al.
Transactions of the American Neurological Association|January 1, 1976
Acid maltase deficiency: reincarnation in cultured muscle fibers of the typical morphological and biochemical defectsV Askanas, W K Engel, S DiMauro, et al.
Annals of Neurology|September 1, 1995
A novel mitochondrial ATPase 6 point mutation in familial bilateral striatal necrosisD Thyagarajan, S Shanske, M Vazquez-Memije, et al.
Muscle & Nerve|September 1, 1996
Molecular basis of muscle phosphoglycerate mutase (PGAM-M) deficiency in the Italian kindredA Toscano, S Tsujino, G Vita, et al.
American Journal of Human Genetics|May 1, 1992
The mitochondrial tRNA(Leu(UUR)) mutation in mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes (MELAS): genetic, biochemical, and morphological correlations in skeletal muscleC T Moraes, E Ricci, E Bonilla, et al.
Neurologia I Neurochirurgia Polska|January 11, 2002
[Pathomechanism and clinical presentation of neurobehavioral disturbances in a patient with MELAS syndrome]M Pachalska, S DiMauro, B D MacQueen, et al.
The Journal of Clinical Investigation|August 1, 1983
Muscle phosphofructokinase deficiency. Biochemical and immunological studies of phosphofructokinase isozymes in muscle cultureM Davidson, A F Miranda, A N Bender, et al.
Nature|May 25, 1989
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop regionM Zeviani, S Servidei, C Gellera, et al.
Annals of Neurology|December 1, 1988
McArdle's disease: biochemical and molecular genetic studiesS Servidei, S Shanske, M Zeviani, et al.
Pageof 43