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M Zeviani

Showing results (21-30 of 184) with videos related to

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Italian Journal of Neurological Sciences|August 11, 2000
Nuclear gene defects in mitochondrial disordersM Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics|November 5, 1999
Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybridsM Toompuu, V Tiranti, M Zeviani, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
The Biochemical Journal|November 15, 1984
Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibresG Salviati, R Betto, D Danieli Betto, et al.
Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.
Human Molecular Genetics|September 25, 1997
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous systemG Battaglia, A Princivalle, F Forti, et al.
International Journal of Clinical Pharmacology Research|December 4, 2004
Accelerated cardiomyopathy in maternally inherited diabetes and deafnessR A Mangiafico, M Zeviani, G Bartoloni, et al.
Journal of Medical Genetics|May 3, 2005
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiencyM Bugiani, V Tiranti, L Farina, et al.
Muscle & Nerve|June 1, 1985
Effects of thyroid hormones on the biochemical specialization of human muscle fibersG Salviati, M Zeviani, R Betto, et al.
Clinical and Experimental Immunology|November 1, 1985
Demonstration and characterization of anti-human mitochondria autoantibodies in idiopathic hypoparathyroidism and in other conditionsC Betterle, A Caretto, M Zeviani, et al.
Pageof 19

Showing results (21-30 of 184) with videos related to

Sort By:
Pageof 19
Italian Journal of Neurological Sciences|August 11, 2000
Nuclear gene defects in mitochondrial disordersM Zeviani, P Corona, L Nijtmans, et al.
Human Molecular Genetics|November 5, 1999
Molecular phenotype of the np 7472 deafness-associated mitochondrial mutation in osteosarcoma cell cybridsM Toompuu, V Tiranti, M Zeviani, et al.
Neurologic Clinics|February 1, 1989
Mitochondrial diseasesM Zeviani, E Bonilla, D C DeVivo, et al.
The Biochemical Journal|November 15, 1984
Myofibrillar-protein isoforms and sarcoplasmic-reticulum Ca2+-transport activity of single human muscle fibresG Salviati, R Betto, D Danieli Betto, et al.
Neurology|January 1, 1987
Benign reversible muscle cytochrome c oxidase deficiency: a second caseM Zeviani, P Peterson, S Servidei, et al.
Human Molecular Genetics|September 25, 1997
Expression of the SMN gene, the spinal muscular atrophy determining gene, in the mammalian central nervous systemG Battaglia, A Princivalle, F Forti, et al.
International Journal of Clinical Pharmacology Research|December 4, 2004
Accelerated cardiomyopathy in maternally inherited diabetes and deafnessR A Mangiafico, M Zeviani, G Bartoloni, et al.
Journal of Medical Genetics|May 3, 2005
Novel mutations in COX15 in a long surviving Leigh syndrome patient with cytochrome c oxidase deficiencyM Bugiani, V Tiranti, L Farina, et al.
Muscle & Nerve|June 1, 1985
Effects of thyroid hormones on the biochemical specialization of human muscle fibersG Salviati, M Zeviani, R Betto, et al.
Clinical and Experimental Immunology|November 1, 1985
Demonstration and characterization of anti-human mitochondria autoantibodies in idiopathic hypoparathyroidism and in other conditionsC Betterle, A Caretto, M Zeviani, et al.
Pageof 19