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DiMauro

Showing results (111-120 of 1,071) with videos related to

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Annals of Neurology|July 1, 1996
Genetic heterogeneity in Leigh syndromeS DiMauro, D C De Vivo
The Journal of Pediatrics|September 1, 1994
Myophosphorylase deficiency: an unusually severe form with myoglobinuriaK Kristjánsson, S Tsujino, S DiMauro
Organic Letters|September 14, 2001
Salen-derived catalysts containing secondary basic groups in the addition of diethylzinc to aldehydesE F DiMauro, M C Kozlowski
Current Rheumatology Reports|August 3, 2010
Metabolic myopathiesSalvatore DiMauro, Caterina Garone, Ali Naini
Annals of the New York Academy of Sciences|May 6, 2004
Mitochondrial encephalomyopathies: diagnostic approachSalvatore Dimauro, Stacey Tay, Michelangelo Mancuso
Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Neurologic Clinics|February 5, 2000
Glycogen storage myopathiesS Tsujino, I Nonaka, S DiMauro
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Laboratory Animal Science|December 1, 1983
Diagnostic exerciseM S Landi, J F DiMauro
Bioorganic & Medicinal Chemistry Letters|June 14, 2017
Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptorsBrian A Sparling, Erin F DiMauro
Pageof 108

Showing results (111-120 of 1,071) with videos related to

Sort By:
Pageof 108
Annals of Neurology|July 1, 1996
Genetic heterogeneity in Leigh syndromeS DiMauro, D C De Vivo
The Journal of Pediatrics|September 1, 1994
Myophosphorylase deficiency: an unusually severe form with myoglobinuriaK Kristjánsson, S Tsujino, S DiMauro
Organic Letters|September 14, 2001
Salen-derived catalysts containing secondary basic groups in the addition of diethylzinc to aldehydesE F DiMauro, M C Kozlowski
Current Rheumatology Reports|August 3, 2010
Metabolic myopathiesSalvatore DiMauro, Caterina Garone, Ali Naini
Annals of the New York Academy of Sciences|May 6, 2004
Mitochondrial encephalomyopathies: diagnostic approachSalvatore Dimauro, Stacey Tay, Michelangelo Mancuso
Revue Neurologique|January 1, 1989
Mitochondrial encephalomyopathiesA Lombes, E Bonilla, S Dimauro
Neurologic Clinics|February 5, 2000
Glycogen storage myopathiesS Tsujino, I Nonaka, S DiMauro
The New England Journal of Medicine|July 22, 1993
Molecular genetic heterogeneity of myophosphorylase deficiency (McArdle's disease)S Tsujino, S Shanske, S DiMauro
Laboratory Animal Science|December 1, 1983
Diagnostic exerciseM S Landi, J F DiMauro
Bioorganic & Medicinal Chemistry Letters|June 14, 2017
Progress in the discovery of small molecule modulators of the Cys-loop superfamily receptorsBrian A Sparling, Erin F DiMauro
Pageof 108