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M P Champion

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Archives of Disease in Childhood|April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosisC J Wilson, M P Champion, J E Collins, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?S Grünewald, L Fairbanks, S Genet, 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.
Archives of Disease in Childhood|November 26, 1997
Serum lactate as a predictor of mortality after paediatric cardiac surgeryM Hatherill, T Sajjanhar, S M Tibby, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Annals of Human Genetics|January 11, 2008
The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East EnglandP Hardelid, M Cortina-Borja, A Munro, et al.
Journal of Inherited Metabolic Disease|May 22, 2007
A novel starch for the treatment of glycogen storage diseasesK Bhattacharya, R C Orton, X Qi, et al.
Journal of Inherited Metabolic Disease|August 21, 2007
High frequency of missense mutations in glycogen storage disease type VIN J Beauchamp, J Taybert, M P Champion, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 24, 2008
Hepatocyte transplantation followed by auxiliary liver transplantation--a novel treatment for ornithine transcarbamylase deficiencyJ Puppi, N Tan, R R Mitry, et al.
Journal of Inherited Metabolic Disease|December 23, 2006
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiencyG S Salomons, C Jakobs, L Landegge Pope, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Archives of Disease in Childhood|April 20, 1999
Outcome of medium chain acyl-CoA dehydrogenase deficiency after diagnosisC J Wilson, M P Champion, J E Collins, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?S Grünewald, L Fairbanks, S Genet, 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.
Archives of Disease in Childhood|November 26, 1997
Serum lactate as a predictor of mortality after paediatric cardiac surgeryM Hatherill, T Sajjanhar, S M Tibby, et al.
Journal of Inherited Metabolic Disease|April 8, 2006
Refining the diagnosis of mitochondrial HMG-CoA synthase deficiencyR Aledo, C Mir, R N Dalton, et al.
Annals of Human Genetics|January 11, 2008
The birth prevalence of PKU in populations of European, South Asian and sub-Saharan African ancestry living in South East EnglandP Hardelid, M Cortina-Borja, A Munro, et al.
Journal of Inherited Metabolic Disease|May 22, 2007
A novel starch for the treatment of glycogen storage diseasesK Bhattacharya, R C Orton, X Qi, et al.
Journal of Inherited Metabolic Disease|August 21, 2007
High frequency of missense mutations in glycogen storage disease type VIN J Beauchamp, J Taybert, M P Champion, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 24, 2008
Hepatocyte transplantation followed by auxiliary liver transplantation--a novel treatment for ornithine transcarbamylase deficiencyJ Puppi, N Tan, R R Mitry, et al.
Journal of Inherited Metabolic Disease|December 23, 2006
Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiencyG S Salomons, C Jakobs, L Landegge Pope, et al.
Pageof 2