C Lamperti|M Zeviani - JoVE Visualize

Showing results (81-90 of 180) with videos related to

Pageof 18

Sort By:

American Journal of Medical Genetics|December 1, 1991

Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.

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|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|February 13, 2002

Women with pregnancy-related polymyositis and high serum CK levels in the newbornS Messina, G Fagiolari, C Lamperti, et al.

Neurology|May 1, 1988

MELAS syndrome: characteristic migrainous and epileptic features and maternal transmissionP Montagna, R Gallassi, R Medori, et al.

Pageof 18

Showing results (81-90 of 180) with videos related to

Sort By:

Pageof 18

American Journal of Medical Genetics|December 1, 1991

Mitochondrial DNA deletion in a girl with manifestations of Kearns-Sayre and Lowe syndromes: an example of phenotypic mimicry?C T Moraes, M Zeviani, E A Schon, et al.

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|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|February 13, 2002

Women with pregnancy-related polymyositis and high serum CK levels in the newbornS Messina, G Fagiolari, C Lamperti, et al.

Neurology|May 1, 1988

MELAS syndrome: characteristic migrainous and epileptic features and maternal transmissionP Montagna, R Gallassi, R Medori, et al.

Pageof 18