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Fernando Scaglia

Showing results (1-10 of 190) with videos related to

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Methods in Molecular Biology (Clifton, N.J.)|January 5, 2012
Nuclear gene defects in mitochondrial disordersFernando Scaglia
Developmental Disabilities Research Reviews|September 7, 2010
The role of mitochondrial dysfunction in psychiatric diseaseFernando Scaglia
Molecular Genetics and Metabolism|March 20, 2010
New insights in nutritional management and amino acid supplementation in urea cycle disordersFernando Scaglia
Molecular Genetics and Metabolism|December 4, 2014
Adult liver disorders caused by inborn errors of metabolism: review and updateSirisak Chanprasert, Fernando Scaglia
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiencyFernando Scaglia, Brendan Lee
Molecular Genetics and Metabolism|June 6, 2008
GM1 gangliosidosis: review of clinical, molecular, and therapeutic aspectsNicola Brunetti-Pierri, Fernando Scaglia
CNS Drugs|June 1, 2006
The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment optionsFernando Scaglia, Jennifer L Northrop
Molecular Genetics and Metabolism|December 15, 2015
Molybdenum cofactor deficiencyPaldeep S Atwal, Fernando Scaglia
Frontiers in Cardiovascular Medicine|August 10, 2016
Mitochondrial CardiomyopathiesAyman W El-Hattab, Fernando Scaglia
Muscle & Nerve|November 14, 2007
Human mitochondrial transfer RNAs: role of pathogenic mutation in diseaseFernando Scaglia, Lee-Jun C Wong
Pageof 19

Showing results (1-10 of 190) with videos related to

Sort By:
Pageof 19
Methods in Molecular Biology (Clifton, N.J.)|January 5, 2012
Nuclear gene defects in mitochondrial disordersFernando Scaglia
Developmental Disabilities Research Reviews|September 7, 2010
The role of mitochondrial dysfunction in psychiatric diseaseFernando Scaglia
Molecular Genetics and Metabolism|March 20, 2010
New insights in nutritional management and amino acid supplementation in urea cycle disordersFernando Scaglia
Molecular Genetics and Metabolism|December 4, 2014
Adult liver disorders caused by inborn errors of metabolism: review and updateSirisak Chanprasert, Fernando Scaglia
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|April 8, 2006
Clinical, biochemical, and molecular spectrum of hyperargininemia due to arginase I deficiencyFernando Scaglia, Brendan Lee
Molecular Genetics and Metabolism|June 6, 2008
GM1 gangliosidosis: review of clinical, molecular, and therapeutic aspectsNicola Brunetti-Pierri, Fernando Scaglia
CNS Drugs|June 1, 2006
The mitochondrial myopathy encephalopathy, lactic acidosis with stroke-like episodes (MELAS) syndrome: a review of treatment optionsFernando Scaglia, Jennifer L Northrop
Molecular Genetics and Metabolism|December 15, 2015
Molybdenum cofactor deficiencyPaldeep S Atwal, Fernando Scaglia
Frontiers in Cardiovascular Medicine|August 10, 2016
Mitochondrial CardiomyopathiesAyman W El-Hattab, Fernando Scaglia
Muscle & Nerve|November 14, 2007
Human mitochondrial transfer RNAs: role of pathogenic mutation in diseaseFernando Scaglia, Lee-Jun C Wong
Pageof 19