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S Dimauro

Showing results (51-60 of 421) with videos related to

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Journal of the Neurological Sciences|August 28, 1999
Disconnection of cerebellar Purkinje cells in Kearns-Sayre syndromeK Tanji, S DiMauro, E Bonilla
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiencyS Tsujino, S Shanske, S DiMauro
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Molecular and Cellular Biochemistry|October 6, 1997
Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of bloodP Kaufmann, M el-Schahawi, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Journal of Bioenergetics and Biomembranes|April 1, 1997
Mitochondrial DNA mutations and pathogenesisE A Schon, E Bonilla, S DiMauro
Annals of Neurology|January 1, 1983
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Transactions of the American Neurological Association|January 1, 1981
Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Revista De Neurologia|April 2, 1999
[Mitochondrial encephalopathies: where are we going?]S DiMauro, A L Andreu, E Bonilla
Pageof 43

Showing results (51-60 of 421) with videos related to

Sort By:
Pageof 43
Journal of the Neurological Sciences|August 28, 1999
Disconnection of cerebellar Purkinje cells in Kearns-Sayre syndromeK Tanji, S DiMauro, E Bonilla
Muscle & Nerve. Supplement|January 1, 1995
Molecular genetic heterogeneity of phosphoglycerate kinase (PGK) deficiencyS Tsujino, S Shanske, S DiMauro
Muscle & Nerve|March 1, 1986
Targeting of lysosomal enzymes: N-acetylglucosamine-1-phosphotransferase during muscle developmentH Den, S Shanske, S DiMauro
Molecular and Cellular Biochemistry|October 6, 1997
Carnitine palmitoyltransferase II deficiency: diagnosis by molecular analysis of bloodP Kaufmann, M el-Schahawi, S DiMauro
Archives of Pediatrics & Adolescent Medicine|November 29, 2001
The other human genomeA L Shanske, S Shanske, S DiMauro
Journal of Bioenergetics and Biomembranes|April 1, 1997
Mitochondrial DNA mutations and pathogenesisE A Schon, E Bonilla, S DiMauro
Annals of Neurology|January 1, 1983
Phosphoglycerate kinase deficiency: another cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Transactions of the American Neurological Association|January 1, 1981
Phosphoglycerate kinase deficiency: a new cause of recurrent myoglobinuriaS DiMauro, M Dalakas, A F Miranda
Advances in Pediatrics|January 1, 1990
Recurrent childhood myoglobinuriaI Tein, S DiMauro, D C DeVivo
Revista De Neurologia|April 2, 1999
[Mitochondrial encephalopathies: where are we going?]S DiMauro, A L Andreu, E Bonilla
Pageof 43