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M Zeviani

Showing results (61-70 of 184) with videos related to

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Neurology|January 1, 1987
Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiencyS Servidei, R P Lazaro, E Bonilla, et al.
American Journal of Human Genetics|February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)M Zeviani, P Amati, N Bresolin, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Effects of pirenzepine on plasma insulin, glucagon and pancreatic polypeptide levels in normal manM Zaccaria, G Giordano, C Pasquali, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
American Journal of Human Genetics|June 12, 1999
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegiaJ Kaukonen, M Zeviani, G P Comi, et al.
Human Molecular Genetics|February 1, 1997
A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndromeM Munaro, V Tiranti, D Sandonà, et al.
Neurology|March 1, 1990
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymesC Gellera, G Uziel, M Rimoldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 25, 2005
Devic's neuromyelitis optica and mitochondrial DNA mutation: a case reportA Ghezzi, S Baldini, M Zaffaroni, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six familiesG Uziel, I Moroni, E Lamantea, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
Pageof 19

Showing results (61-70 of 184) with videos related to

Sort By:
Pageof 19
Neurology|January 1, 1987
Mitochondrial encephalomyopathy and partial cytochrome c oxidase deficiencyS Servidei, R P Lazaro, E Bonilla, et al.
American Journal of Human Genetics|February 1, 1991
Rapid detection of the A----G(8344) mutation of mtDNA in Italian families with myoclonus epilepsy and ragged-red fibers (MERRF)M Zeviani, P Amati, N Bresolin, et al.
European Journal of Clinical Pharmacology|January 1, 1985
Effects of pirenzepine on plasma insulin, glucagon and pancreatic polypeptide levels in normal manM Zaccaria, G Giordano, C Pasquali, et al.
Annals of Neurology|July 1, 1990
Tissue distribution and transmission of mitochondrial DNA deletions in mitochondrial myopathiesM Zeviani, C Gellera, M Pannacci, et al.
American Journal of Human Genetics|June 12, 1999
A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegiaJ Kaukonen, M Zeviani, G P Comi, et al.
Human Molecular Genetics|February 1, 1997
A single cell complementation class is common to several cases of cytochrome c oxidase-defective Leigh's syndromeM Munaro, V Tiranti, D Sandonà, et al.
Neurology|March 1, 1990
Fumarase deficiency is an autosomal recessive encephalopathy affecting both the mitochondrial and the cytosolic enzymesC Gellera, G Uziel, M Rimoldi, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|February 25, 2005
Devic's neuromyelitis optica and mitochondrial DNA mutation: a case reportA Ghezzi, S Baldini, M Zaffaroni, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 1, 1997
Mitochondrial disease associated with the T8993G mutation of the mitochondrial ATPase 6 gene: a clinical, biochemical, and molecular study in six familiesG Uziel, I Moroni, E Lamantea, et al.
Biochemical Society Transactions|August 1, 1985
Cytochrome c oxidase deficiencyS DiMauro, M Zeviani, E Bonilla, et al.
Pageof 19