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M Zeviani

Showing results (91-100 of 184) with videos related to

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Journal of Medical Genetics|May 4, 2004
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genomeA Limongelli, J Schaefer, S Jackson, et al.
Neurology|November 1, 1993
Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patientsS DiDonato, M Zeviani, P Giovannini, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 geneC Dionisi-Vici, S Seneca, M Zeviani, et al.
Human Molecular Genetics|November 1, 1995
Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformantsV Tiranti, M Munaro, D Sandonà, et al.
Neurology|December 17, 1998
Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988M Zeviani, C T Moraes, S DiMauro, et al.
Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.
American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.
Genomics|January 20, 1995
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.
Neurology|May 1, 1988
MELAS syndrome: characteristic migrainous and epileptic features and maternal transmissionP Montagna, R Gallassi, R Medori, et al.
Journal of Medical Genetics|April 5, 2003
The role of APOE in the phenotypic expression of Leber hereditary optic neuropathyP Yu-Wai-Man, C M Morris, M Zeviani, et al.
Pageof 19

Showing results (91-100 of 184) with videos related to

Sort By:
Pageof 19
Journal of Medical Genetics|May 4, 2004
Variable penetrance of a familial progressive necrotising encephalopathy due to a novel tRNA(Ile) homoplasmic mutation in the mitochondrial genomeA Limongelli, J Schaefer, S Jackson, et al.
Neurology|November 1, 1993
Respiratory chain and mitochondrial DNA in muscle and brain in Parkinson's disease patientsS DiDonato, M Zeviani, P Giovannini, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Fulminant Leigh syndrome and sudden unexpected death in a family with the T9176C mutation of the mitochondrial ATPase 6 geneC Dionisi-Vici, S Seneca, M Zeviani, et al.
Human Molecular Genetics|November 1, 1995
Nuclear DNA origin of cytochrome c oxidase deficiency in Leigh's syndrome: genetic evidence based on patient's-derived rho degrees transformantsV Tiranti, M Munaro, D Sandonà, et al.
Neurology|December 17, 1998
Deletions of mitochondrial DNA in Kearns-Sayre syndrome. 1988M Zeviani, C T Moraes, S DiMauro, et al.
Neurology|September 1, 1988
Deletions of mitochondrial DNA in Kearns-Sayre syndromeM Zeviani, C T Moraes, S DiMauro, et al.
American Journal of Medical Genetics|February 2, 1996
X-inactivation patterns in female Leber's hereditary optic neuropathy patients do not support a strong X-linked determinantE Pegoraro, V Carelli, M Zeviani, et al.
Genomics|January 20, 1995
Chromosomal localization of mitochondrial transcription factor A (TCF6), single-stranded DNA-binding protein (SSBP), and endonuclease G (ENDOG), three human housekeeping genes involved in mitochondrial biogenesisV Tiranti, E Rossi, A Ruiz-Carrillo, et al.
Neurology|May 1, 1988
MELAS syndrome: characteristic migrainous and epileptic features and maternal transmissionP Montagna, R Gallassi, R Medori, et al.
Journal of Medical Genetics|April 5, 2003
The role of APOE in the phenotypic expression of Leber hereditary optic neuropathyP Yu-Wai-Man, C M Morris, M Zeviani, et al.
Pageof 19