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Gerard T Berry

Showing results (1-10 of 138) with videos related to

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Nestle Nutrition Workshop Series. Paediatric Programme|July 16, 2008
Metabolic profilingGerard T Berry
Journal of Inherited Metabolic Disease|November 19, 2008
The unexplored potential of the pentose phosphate pathway in health and diseaseGerard T Berry
Journal of Inherited Metabolic Disease|January 20, 2011
Is prenatal myo-inositol deficiency a mechanism of CNS injury in galactosemia?Gerard T Berry
Annals of the New York Academy of Sciences|June 25, 2008
Galactosemia and amenorrhea in the adolescentGerard T Berry
Molecular Genetics and Metabolism Reports|March 1, 2017
Phenotypic heterogeneity of a compound heterozygous SUCLA2 mutationGerard T Berry
Molecular Genetics and Metabolism|April 10, 2012
Galactosemia: when is it a newborn screening emergency?Gerard T Berry
Journal of Inherited Metabolic Disease|December 1, 2010
Introduction to the Maastricht workshop: lessons from the past and new directions in galactosemiaGerard T Berry, Louis J Elsas
JIMD Reports|May 1, 2016
N-Acetylcysteine Therapy in an Infant with Transaldolase Deficiency Is Well Tolerated and Associated with Normalization of Alpha Fetoprotein LevelsLance H Rodan, Gerard T Berry
Methods in Molecular Biology (Clifton, N.J.)|September 19, 2009
Brain phosphoinositide extraction, fractionation, and analysis by MALDI-TOF MSRoy A Johanson, Gerard T Berry
Molecular Genetics and Metabolism|July 26, 2022
Pathophysiology of long-term complications in classic galactosemia: What we do and do not knowJudith L Fridovich-Keil, Gerard T Berry
Pageof 14

Showing results (1-10 of 138) with videos related to

Sort By:
Pageof 14
Nestle Nutrition Workshop Series. Paediatric Programme|July 16, 2008
Metabolic profilingGerard T Berry
Journal of Inherited Metabolic Disease|November 19, 2008
The unexplored potential of the pentose phosphate pathway in health and diseaseGerard T Berry
Journal of Inherited Metabolic Disease|January 20, 2011
Is prenatal myo-inositol deficiency a mechanism of CNS injury in galactosemia?Gerard T Berry
Annals of the New York Academy of Sciences|June 25, 2008
Galactosemia and amenorrhea in the adolescentGerard T Berry
Molecular Genetics and Metabolism Reports|March 1, 2017
Phenotypic heterogeneity of a compound heterozygous SUCLA2 mutationGerard T Berry
Molecular Genetics and Metabolism|April 10, 2012
Galactosemia: when is it a newborn screening emergency?Gerard T Berry
Journal of Inherited Metabolic Disease|December 1, 2010
Introduction to the Maastricht workshop: lessons from the past and new directions in galactosemiaGerard T Berry, Louis J Elsas
JIMD Reports|May 1, 2016
N-Acetylcysteine Therapy in an Infant with Transaldolase Deficiency Is Well Tolerated and Associated with Normalization of Alpha Fetoprotein LevelsLance H Rodan, Gerard T Berry
Methods in Molecular Biology (Clifton, N.J.)|September 19, 2009
Brain phosphoinositide extraction, fractionation, and analysis by MALDI-TOF MSRoy A Johanson, Gerard T Berry
Molecular Genetics and Metabolism|July 26, 2022
Pathophysiology of long-term complications in classic galactosemia: What we do and do not knowJudith L Fridovich-Keil, Gerard T Berry
Pageof 14