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J Raiman

Showing results (11-20 of 22) with videos related to

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JIMD Reports|August 27, 2014
Clinical, Biochemical, and Molecular Presentation in a Patient with the cblD-Homocystinuria Inborn Error of Cobalamin MetabolismCelia Atkinson, Isabelle R Miousse, David Watkins, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 4, 2019
The utility of dried blood spot monitoring of branched-chain amino acids for maple syrup urine disease: A retrospective chart review studyJ Kaur, L Nagy, B Wan, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 19, 2007
Auxiliary liver transplantation for propionic acidemia: a 10-year follow-upM Rela, N Battula, M Madanur, et al.
British Journal of Anaesthesia|February 21, 2008
Mitochondrial disorders and general anaesthesia: a case series and reviewE J Footitt, M D Sinha, J A J Raiman, et al.
AAPS Pharmscitech|January 20, 2004
Process analysis of fluidized bed granulationJ Rantanen, A Jørgensen, E Räsänen, et al.
Developmental Medicine and Child Neurology|August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiencyR M Brown, R A Head, A A M Morris, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2026
Liver Transplantation for Inherited Metabolic Disorders: A Work in ProgressV Sreekantam, K Kurkal, S Santra, et al.
Molecular Genetics and Metabolism|August 7, 2019
Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in EnglandA Broomfield, J Davison, J Roberts, et al.
Plos One|July 5, 2013
Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERTSuhrad G Banugaria, Sean N Prater, Trusha T Patel, et al.
Pageof 3

Showing results (11-20 of 22) with videos related to

Sort By:
Pageof 3
JIMD Reports|August 27, 2014
Clinical, Biochemical, and Molecular Presentation in a Patient with the cblD-Homocystinuria Inborn Error of Cobalamin MetabolismCelia Atkinson, Isabelle R Miousse, David Watkins, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|November 4, 2019
The utility of dried blood spot monitoring of branched-chain amino acids for maple syrup urine disease: A retrospective chart review studyJ Kaur, L Nagy, B Wan, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|August 19, 2007
Auxiliary liver transplantation for propionic acidemia: a 10-year follow-upM Rela, N Battula, M Madanur, et al.
British Journal of Anaesthesia|February 21, 2008
Mitochondrial disorders and general anaesthesia: a case series and reviewE J Footitt, M D Sinha, J A J Raiman, et al.
AAPS Pharmscitech|January 20, 2004
Process analysis of fluidized bed granulationJ Rantanen, A Jørgensen, E Räsänen, et al.
Developmental Medicine and Child Neurology|August 15, 2006
Pyruvate dehydrogenase E3 binding protein (protein X) deficiencyR M Brown, R A Head, A A M Morris, et al.
Human Genetics|February 3, 2009
Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotypeJ M Cameron, M Maj, V Levandovskiy, et al.
Acta Paediatrica (Oslo, Norway : 1992)|March 30, 2026
Liver Transplantation for Inherited Metabolic Disorders: A Work in ProgressV Sreekantam, K Kurkal, S Santra, et al.
Molecular Genetics and Metabolism|August 7, 2019
Ten years of enzyme replacement therapy in paediatric onset mucopolysaccharidosis II in EnglandA Broomfield, J Davison, J Roberts, et al.
Plos One|July 5, 2013
Algorithm for the early diagnosis and treatment of patients with cross reactive immunologic material-negative classic infantile pompe disease: a step towards improving the efficacy of ERTSuhrad G Banugaria, Sean N Prater, Trusha T Patel, et al.
Pageof 3