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A Chakrapani

Showing results (21-30 of 31) with videos related to

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Archives of Disease in Childhood|March 21, 2006
Protein substitute dosage in PKU: how much do young patients need?A MacDonald, A Chakrapani, C Hendriksz, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|August 1, 2012
Dietary practices in glutaric aciduria type 1 over 16 yearsH Gokmen-Ozel, A MacDonald, A Daly, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
'Ready to drink' protein substitute is easier is for people with phenylketonuriaA MacDonald, M Lilburn, P Davies, et al.
Journal of Inherited Metabolic Disease|October 23, 2008
Long-term compliance with a novel vitamin and mineral supplement in older people with PKUA MacDonald, P Lee, P Davies, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
A new, low-volume protein substitute for teenagers and adults with phenylketonuriaA MacDonald, M Lilburn, B Cochrane, et al.
Journal of Inherited Metabolic Disease|June 12, 2009
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UKT Hutchin, M A Preece, C Hendriksz, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 17, 2015
Early and late complications after liver transplantation for propionic acidemia in children: a two centers studyF Charbit-Henrion, F Lacaille, P McKiernan, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, 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.
Pageof 4

Showing results (21-30 of 31) with videos related to

Sort By:
Pageof 4
Archives of Disease in Childhood|March 21, 2006
Protein substitute dosage in PKU: how much do young patients need?A MacDonald, A Chakrapani, C Hendriksz, et al.
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|August 1, 2012
Dietary practices in glutaric aciduria type 1 over 16 yearsH Gokmen-Ozel, A MacDonald, A Daly, et al.
Journal of Inherited Metabolic Disease|June 1, 2006
'Ready to drink' protein substitute is easier is for people with phenylketonuriaA MacDonald, M Lilburn, P Davies, et al.
Journal of Inherited Metabolic Disease|October 23, 2008
Long-term compliance with a novel vitamin and mineral supplement in older people with PKUA MacDonald, P Lee, P Davies, et al.
Journal of Inherited Metabolic Disease|May 26, 2004
A new, low-volume protein substitute for teenagers and adults with phenylketonuriaA MacDonald, M Lilburn, B Cochrane, et al.
Journal of Inherited Metabolic Disease|June 12, 2009
Neonatal intrahepatic cholestasis caused by citrin deficiency (NICCD) as a cause of liver disease in infants in the UKT Hutchin, M A Preece, C Hendriksz, et al.
American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|February 17, 2015
Early and late complications after liver transplantation for propionic acidemia in children: a two centers studyF Charbit-Henrion, F Lacaille, P McKiernan, et al.
Journal of Internal Medicine|November 21, 2008
Severe HDL deficiency due to novel defects in the ABCA1 transporterL Pisciotta, L Bocchi, C Candini, et al.
Journal of Inherited Metabolic Disease|May 20, 2005
Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiencyS E Olpin, S Clark, B S Andresen, 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.
Pageof 4