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Gerard T Berry

Showing results (41-50 of 138) with videos related to

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Molecular Genetics and Metabolism|November 18, 2005
Elements of diabetic nephropathy in a patient with GLUT 2 deficiencyGerard T Berry, John W Baynes, Kevin J Wells-Knecht, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Menkes disease in affected females: the clinical disease spectrumPatroula Smpokou, Monisha Samanta, Gerard T Berry, et al.
Clinical Biochemistry|September 14, 2012
Recurrent unexplained hyperammonemia in an adolescent with arginase deficiencyYan Zhang, Yuval E Landau, David T Miller, et al.
Molecular Genetics and Metabolism|September 16, 2023
The treatment of biochemical genetic diseases: From substrate reduction to nucleic acid therapiesE Naomi Vos, Didem Demirbas, Matthew Mangel, et al.
Molecular Genetics and Metabolism|August 15, 2021
Transient developmental delays in infants with Duarte-2 variant galactosemiaSusan E Waisbren, Catherine Tran, Didem Demirbas, et al.
Forensic Science, Medicine, and Pathology|July 16, 2013
Witnessed sleep-related seizure and sudden unexpected death in infancy: a case reportHannah C Kinney, Anna G McDonald, Megan E Minter, et al.
Neuroradiology|May 9, 2003
MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensationWajanat Jan, Robert A Zimmerman, Zhiyue J Wang, et al.
The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Journal of Agricultural and Food Chemistry|January 25, 2014
Galactose content of legumes, caseinates, and some hard cheeses: implications for diet treatment of classic galactosemiaSandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, et al.
Molecular Genetics and Metabolism|May 27, 2014
A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemiaSandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, et al.
Pageof 14

Showing results (41-50 of 138) with videos related to

Sort By:
Pageof 14
Molecular Genetics and Metabolism|November 18, 2005
Elements of diabetic nephropathy in a patient with GLUT 2 deficiencyGerard T Berry, John W Baynes, Kevin J Wells-Knecht, et al.
American Journal of Medical Genetics. Part A|November 28, 2014
Menkes disease in affected females: the clinical disease spectrumPatroula Smpokou, Monisha Samanta, Gerard T Berry, et al.
Clinical Biochemistry|September 14, 2012
Recurrent unexplained hyperammonemia in an adolescent with arginase deficiencyYan Zhang, Yuval E Landau, David T Miller, et al.
Molecular Genetics and Metabolism|September 16, 2023
The treatment of biochemical genetic diseases: From substrate reduction to nucleic acid therapiesE Naomi Vos, Didem Demirbas, Matthew Mangel, et al.
Molecular Genetics and Metabolism|August 15, 2021
Transient developmental delays in infants with Duarte-2 variant galactosemiaSusan E Waisbren, Catherine Tran, Didem Demirbas, et al.
Forensic Science, Medicine, and Pathology|July 16, 2013
Witnessed sleep-related seizure and sudden unexpected death in infancy: a case reportHannah C Kinney, Anna G McDonald, Megan E Minter, et al.
Neuroradiology|May 9, 2003
MR diffusion imaging and MR spectroscopy of maple syrup urine disease during acute metabolic decompensationWajanat Jan, Robert A Zimmerman, Zhiyue J Wang, et al.
The New England Journal of Medicine|June 1, 2007
Survival after treatment with phenylacetate and benzoate for urea-cycle disordersGregory M Enns, Susan A Berry, Gerard T Berry, et al.
Journal of Agricultural and Food Chemistry|January 25, 2014
Galactose content of legumes, caseinates, and some hard cheeses: implications for diet treatment of classic galactosemiaSandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, et al.
Molecular Genetics and Metabolism|May 27, 2014
A re-evaluation of life-long severe galactose restriction for the nutrition management of classic galactosemiaSandra C Van Calcar, Laurie E Bernstein, Frances J Rohr, et al.
Pageof 14