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R J Pollitt

Showing results (111-120 of 133) with videos related to

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Pediatric Research|July 1, 1990
D(+)-glyceric aciduria: etiology and clinical consequencesJ R Bonham, T J Stephenson, K H Carpenter, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Carnitine-acylcarnitine translocase deficiency--a mild phenotypeS E Olpin, J R Bonham, M Downing, et al.
The Veterinary Record|July 8, 1989
Primary hyperoxaluria (L-glyceric aciduria) in the cat: a newly recognised inherited diseaseR E McKerrell, W F Blakemore, M F Heath, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old manS E Olpin, R J Pollitt, J McMenamin, et al.
Progress in Clinical and Biological Research|January 1, 1992
Pathophysiological approach to carnitine palmitoyltransferase II deficienciesF Demaugre, J P Bonnefont, M Brivet, et al.
European Journal of Pediatrics|May 1, 1993
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patientR Moore, J F Glasgow, M A Bingham, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatallyM J Bennett, D A Curnock, P C Engel, et al.
Acta Neurologica Belgica|January 1, 1976
[Pathological and biochemical studies on a neonatal case of argininosuccinic aciduria (author's transl)]J P Farriaux, J L Dhondt, P Formstecher, et al.
Annales De Genetique|March 1, 1976
[Attempt at antenatal diagnosis of argininosuccinic aciduria]J L Dhondt, J P Farriaux, R J Pollitt, et al.
Pageof 14

Showing results (111-120 of 133) with videos related to

Sort By:
Pageof 14
Pediatric Research|July 1, 1990
D(+)-glyceric aciduria: etiology and clinical consequencesJ R Bonham, T J Stephenson, K H Carpenter, et al.
Journal of Inherited Metabolic Disease|November 5, 1997
Carnitine-acylcarnitine translocase deficiency--a mild phenotypeS E Olpin, J R Bonham, M Downing, et al.
The Veterinary Record|July 8, 1989
Primary hyperoxaluria (L-glyceric aciduria) in the cat: a newly recognised inherited diseaseR E McKerrell, W F Blakemore, M F Heath, et al.
Journal of Inherited Metabolic Disease|January 31, 2003
2-methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old manS E Olpin, R J Pollitt, J McMenamin, et al.
Progress in Clinical and Biological Research|January 1, 1992
Pathophysiological approach to carnitine palmitoyltransferase II deficienciesF Demaugre, J P Bonnefont, M Brivet, et al.
European Journal of Pediatrics|May 1, 1993
Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patientR Moore, J F Glasgow, M A Bingham, et al.
Journal of Inherited Metabolic Disease|January 1, 1990
Analysis of abnormal urinary metabolites in the newborn period in medium-chain acyl-CoA dehydrogenase deficiencyM J Bennett, P M Coates, D E Hale, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
Glutaric aciduria type II: biochemical investigation and treatment of a child diagnosed prenatallyM J Bennett, D A Curnock, P C Engel, et al.
Acta Neurologica Belgica|January 1, 1976
[Pathological and biochemical studies on a neonatal case of argininosuccinic aciduria (author's transl)]J P Farriaux, J L Dhondt, P Formstecher, et al.
Annales De Genetique|March 1, 1976
[Attempt at antenatal diagnosis of argininosuccinic aciduria]J L Dhondt, J P Farriaux, R J Pollitt, et al.
Pageof 14