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Bryan E Hainline

Showing results (1-10 of 14) with videos related to

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Chest|October 16, 2007
Hyperammonemia in the ICUAlison S Clay, Bryan E Hainline
JIMD Reports|May 12, 2021
Consideration of a metabolic disorder in the differential of mild developmental delay: A case of nonketotic hyperglycinemia revisited 36 years laterTimothy F Tramontana, Theodore E Wilson, Bryan E Hainline
Pediatric Neurology|December 16, 2014
An atypical case of Canavan disease with stroke-like presentationKatherine E Delaney, Stephen F Kralik, Bryan E Hainline, et al.
Pediatrics|June 8, 2011
Neonatal Graves' disease associated with severe metabolic abnormalitiesKatherine A Lewis, William Engle, Bryan E Hainline, et al.
The Journal of Pediatrics|November 1, 2002
Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutationsGeorgirene D Vladutiu, Elizabeth J Quackenbush, Bryan E Hainline, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 4, 2007
Class selection of amino acid metabolites in body fluids using chemical derivatization and their enhanced 13C NMRNarasimhamurthy Shanaiah, M Aruni Desilva, G A Nagana Gowda, et al.
Analytical and Bioanalytical Chemistry|July 6, 2006
Principal component analysis of urine metabolites detected by NMR and DESI-MS in patients with inborn errors of metabolismZhengzheng Pan, Haiwei Gu, Nari Talaty, et al.
NMR in Biomedicine|May 15, 2009
1H NMR metabolomics study of age profiling in childrenHaiwei Gu, Zhengzheng Pan, Bowei Xi, et al.
Molecular Genetics and Metabolism|October 3, 2002
Pyruvate carboxylase deficiency--insights from liver transplantationWilliam L Nyhan, Ajai Khanna, Bruce A Barshop, et al.
Molecular Genetics and Metabolism|May 19, 2023
Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoinM Laura Duque Lasio, Angela C Leshinski, Nicole H Ducich, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Chest|October 16, 2007
Hyperammonemia in the ICUAlison S Clay, Bryan E Hainline
JIMD Reports|May 12, 2021
Consideration of a metabolic disorder in the differential of mild developmental delay: A case of nonketotic hyperglycinemia revisited 36 years laterTimothy F Tramontana, Theodore E Wilson, Bryan E Hainline
Pediatric Neurology|December 16, 2014
An atypical case of Canavan disease with stroke-like presentationKatherine E Delaney, Stephen F Kralik, Bryan E Hainline, et al.
Pediatrics|June 8, 2011
Neonatal Graves' disease associated with severe metabolic abnormalitiesKatherine A Lewis, William Engle, Bryan E Hainline, et al.
The Journal of Pediatrics|November 1, 2002
Lethal neonatal and severe late infantile forms of carnitine palmitoyltransferase II deficiency associated with compound heterozygosity for different protein truncation mutationsGeorgirene D Vladutiu, Elizabeth J Quackenbush, Bryan E Hainline, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 4, 2007
Class selection of amino acid metabolites in body fluids using chemical derivatization and their enhanced 13C NMRNarasimhamurthy Shanaiah, M Aruni Desilva, G A Nagana Gowda, et al.
Analytical and Bioanalytical Chemistry|July 6, 2006
Principal component analysis of urine metabolites detected by NMR and DESI-MS in patients with inborn errors of metabolismZhengzheng Pan, Haiwei Gu, Nari Talaty, et al.
NMR in Biomedicine|May 15, 2009
1H NMR metabolomics study of age profiling in childrenHaiwei Gu, Zhengzheng Pan, Bowei Xi, et al.
Molecular Genetics and Metabolism|October 3, 2002
Pyruvate carboxylase deficiency--insights from liver transplantationWilliam L Nyhan, Ajai Khanna, Bruce A Barshop, et al.
Molecular Genetics and Metabolism|May 19, 2023
Clinical, biochemical and molecular characterization of 12 patients with pyruvate carboxylase deficiency treated with triheptanoinM Laura Duque Lasio, Angela C Leshinski, Nicole H Ducich, et al.
Pageof 2