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DiMauro

Showing results (621-630 of 942) with videos related to

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Journal of Affective Disorders|June 26, 2007
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a familyMichelangelo Mancuso, Giulia Ricci, Anna Choub, et al.
Neurology|January 1, 1984
Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activityJ E Riggs, S S Schochet, A V Fakadej, et al.
American Journal of Human Genetics|July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993S L White, V R Collins, R Wolfe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
Archives of Neurology|March 12, 2008
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 casesSara Shanske, Jorida Coku, Jiesheng Lu, et al.
Neurology|January 27, 1998
Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogenesesR Carrozzo, M Hirano, B Fromenty, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.
Nucleic Acids Research|February 11, 1990
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNAS Mita, R Rizzuto, C T Moraes, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 2025
Solvation-induced local structure in liquids probed by high-harmonic spectroscopyEric Moore, Sucharita Giri, Andreas Koutsogiannis, et al.
Pageof 95

Showing results (621-630 of 942) with videos related to

Sort By:
Pageof 95
Journal of Affective Disorders|June 26, 2007
Autosomal dominant psychiatric disorders and mitochondrial DNA multiple deletions: report of a familyMichelangelo Mancuso, Giulia Ricci, Anna Choub, et al.
Neurology|January 1, 1984
Mitochondrial encephalomyopathy with decreased succinate-cytochrome c reductase activityJ E Riggs, S S Schochet, A V Fakadej, et al.
American Journal of Human Genetics|July 27, 1999
Genetic counseling and prenatal diagnosis for the mitochondrial DNA mutations at nucleotide 8993S L White, V R Collins, R Wolfe, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 7, 1999
Early onset of diabetes mellitus associated with the mitochondrial DNA T14709C point mutation: patient report and literature reviewM E Damore, P W Speiser, A E Slonim, et al.
Archives of Neurology|March 12, 2008
The G13513A mutation in the ND5 gene of mitochondrial DNA as a common cause of MELAS or Leigh syndrome: evidence from 12 casesSara Shanske, Jorida Coku, Jiesheng Lu, et al.
Neurology|January 27, 1998
Multiple mtDNA deletions features in autosomal dominant and recessive diseases suggest distinct pathogenesesR Carrozzo, M Hirano, B Fromenty, et al.
Annals of Neurology|January 1, 1993
Glycogen branching enzyme deficiency in adult polyglucosan body diseaseC Bruno, S Servidei, S Shanske, et al.
Neurology|October 1, 1988
Immunocytochemical study of nebulin in Duchenne muscular dystrophyE Bonilla, A F Miranda, A Prelle, et al.
Nucleic Acids Research|February 11, 1990
Recombination via flanking direct repeats is a major cause of large-scale deletions of human mitochondrial DNAS Mita, R Rizzuto, C T Moraes, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 25, 2025
Solvation-induced local structure in liquids probed by high-harmonic spectroscopyEric Moore, Sucharita Giri, Andreas Koutsogiannis, et al.
Pageof 95