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M Zeviani

Showing results (111-120 of 184) with videos related to

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The New England Journal of Medicine|January 8, 1987
Is nebulin the defective gene product in Duchenne muscular dystrophy?D S Wood, M Zeviani, A Prelle, et al.
Annals of Neurology|January 10, 2002
Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentationsP Corona, E Lamantea, M Greco, et al.
Gene|May 15, 1988
Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidaseM Zeviani, S Sakoda, A A Sherbany, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2012
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutationEnrico Saracchi, J C Difrancesco, L Brighina, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
Science (New York, N.Y.)|August 5, 2000
Role of adenine nucleotide translocator 1 in mtDNA maintenanceJ Kaukonen, J K Juselius, V Tiranti, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutationsB Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Neurology|May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathyM Bugiani, S Al Shahwan, E Lamantea, et al.
Neurology|June 27, 2002
NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathyP Yu-Wai-Man, D T Brown, M S Wehnert, et al.
Journal of the Neurological Sciences|April 1, 1995
Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiencyC Antozzi, S Franceschetti, G Filippini, et al.
Pageof 19

Showing results (111-120 of 184) with videos related to

Sort By:
Pageof 19
The New England Journal of Medicine|January 8, 1987
Is nebulin the defective gene product in Duchenne muscular dystrophy?D S Wood, M Zeviani, A Prelle, et al.
Annals of Neurology|January 10, 2002
Novel heteroplasmic mtDNA mutation in a family with heterogeneous clinical presentationsP Corona, E Lamantea, M Greco, et al.
Gene|May 15, 1988
Sequence of cDNAs encoding subunit Vb of human and bovine cytochrome c oxidaseM Zeviani, S Sakoda, A A Sherbany, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|March 20, 2012
A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutationEnrico Saracchi, J C Difrancesco, L Brighina, et al.
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
Science (New York, N.Y.)|August 5, 2000
Role of adenine nucleotide translocator 1 in mtDNA maintenanceJ Kaukonen, J K Juselius, V Tiranti, et al.
Journal of Inherited Metabolic Disease|August 11, 2004
GTP-cyclohydrolase I gene mutations in patients with autosomal dominant and recessive GTP-CH1 deficiency: identification and functional characterization of four novel mutationsB Garavaglia, F Invernizzi, M L Agostoni Carbone, et al.
Neurology|May 19, 2006
GJA12 mutations in children with recessive hypomyelinating leukoencephalopathyM Bugiani, S Al Shahwan, E Lamantea, et al.
Neurology|June 27, 2002
NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathyP Yu-Wai-Man, D T Brown, M S Wehnert, et al.
Journal of the Neurological Sciences|April 1, 1995
Epilepsia partialis continua associated with NADH-coenzyme Q reductase deficiencyC Antozzi, S Franceschetti, G Filippini, et al.
Pageof 19