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Gerard T Berry

Showing results (11-20 of 138) with videos related to

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Epilepsia|February 12, 2021
Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?Gerard T Berry, Hudson H Freeze, Eva Morava
Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Hepatopathy: Metabolism Defects of Galactose, Fructose, and TyrosineDidem Demirbas, William J Brucker, Gerard T Berry
JIMD Reports|November 12, 2021
Paroxysmal hyperthermia, dysautonomia and rhabdomyolysis in a patient with Lesch-Nyhan syndromeMandeep Rana, Karen Cuttin, Gerard T Berry, et al.
Current Opinion in Clinical Nutrition and Metabolic Care|May 24, 2015
Galactose metabolism and healthAna I Coelho, Gerard T Berry, M Estela Rubio-Gozalbo
JIMD Reports|June 14, 2016
Hydroxysteroid 17-Beta Dehydrogenase Type 10 Disease in SiblingsAnnely Richardson, Gerard T Berry, Cheryl Garganta, et al.
JIMD Reports|June 22, 2016
Erratum to: Disease Heterogeneity in Na<sup>+</sup>/Citrate Cotransporter DeficiencyIrina Anselm, Morgan MacCuaig, Sanjay P Prabhu, et al.
Molecular Genetics and Metabolism|April 28, 2004
Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brainGerard T Berry, Roberto Buccafusca, John J Greer, et al.
JIMD Reports|March 11, 2016
Disease Heterogeneity in Na<sup>+</sup>/Citrate Cotransporter DeficiencyIrina Anselm, Morgan MacCuaig, Sanjay B Prabhu, et al.
Molecular Genetics and Metabolism|June 3, 2004
Extended [13C]galactose oxidation studies in patients with galactosemiaGerard T Berry, Robert A Reynolds, Claire T Yager, et al.
Pediatric Emergency Care|March 30, 2017
Acute Illness Protocol for Fatty Acid Oxidation and Carnitine DisordersSaud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pageof 14

Showing results (11-20 of 138) with videos related to

Sort By:
Pageof 14
Epilepsia|February 12, 2021
Is X-linked, infantile onset ALG13-related developmental and epileptic encephalopathy a congenital disorder of glycosylation?Gerard T Berry, Hudson H Freeze, Eva Morava
Pediatric Clinics of North America|March 6, 2018
Inborn Errors of Metabolism with Hepatopathy: Metabolism Defects of Galactose, Fructose, and TyrosineDidem Demirbas, William J Brucker, Gerard T Berry
JIMD Reports|November 12, 2021
Paroxysmal hyperthermia, dysautonomia and rhabdomyolysis in a patient with Lesch-Nyhan syndromeMandeep Rana, Karen Cuttin, Gerard T Berry, et al.
Current Opinion in Clinical Nutrition and Metabolic Care|May 24, 2015
Galactose metabolism and healthAna I Coelho, Gerard T Berry, M Estela Rubio-Gozalbo
JIMD Reports|June 14, 2016
Hydroxysteroid 17-Beta Dehydrogenase Type 10 Disease in SiblingsAnnely Richardson, Gerard T Berry, Cheryl Garganta, et al.
JIMD Reports|June 22, 2016
Erratum to: Disease Heterogeneity in Na<sup>+</sup>/Citrate Cotransporter DeficiencyIrina Anselm, Morgan MacCuaig, Sanjay P Prabhu, et al.
Molecular Genetics and Metabolism|April 28, 2004
Phosphoinositide deficiency due to inositol depletion is not a mechanism of lithium action in brainGerard T Berry, Roberto Buccafusca, John J Greer, et al.
JIMD Reports|March 11, 2016
Disease Heterogeneity in Na<sup>+</sup>/Citrate Cotransporter DeficiencyIrina Anselm, Morgan MacCuaig, Sanjay B Prabhu, et al.
Molecular Genetics and Metabolism|June 3, 2004
Extended [13C]galactose oxidation studies in patients with galactosemiaGerard T Berry, Robert A Reynolds, Claire T Yager, et al.
Pediatric Emergency Care|March 30, 2017
Acute Illness Protocol for Fatty Acid Oxidation and Carnitine DisordersSaud H Aldubayan, Lance H Rodan, Gerard T Berry, et al.
Pageof 14