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J B de Klerk

Showing results (1-10 of 48) with videos related to

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Tijdschrift Voor Kindergeneeskunde|June 1, 1983
[A patient with neonatal citrullinemia]M Berghuis, B P Cats, J B de Klerk, et al.
European Journal of Pediatrics|March 1, 1996
Sudden infant death and lysinuric protein intoleranceJ B de Klerk, M Duran, J G Huijmans, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1987
[Reye's syndrome]M Berghuis, A J van Vught, J B de Klerk, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.
Clinical Chemistry|March 1, 1988
Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiencyM Duran, L Bruinvis, D Ketting, et al.
Neuropediatrics|May 1, 1990
Quasi-moyamoya disease and heterozygosity for homocystinuria in a five-year-old girlR van Diemen-Steenvoorde, O van Nieuwenhuizen, J B de Klerk, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Maternal PKU syndrome in an exceptional family with unexpected PKUJ B De Klerk, S K Wadman, H J Dijkhuis, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyH Przyrembel, C Jakobs, L IJlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disordersR J Wanders, L Ijlst, E van Elk, et al.
Archives of Dermatology|September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant ricketsA P Oranje, H Przyrembel, M Meradji, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Tijdschrift Voor Kindergeneeskunde|June 1, 1983
[A patient with neonatal citrullinemia]M Berghuis, B P Cats, J B de Klerk, et al.
European Journal of Pediatrics|March 1, 1996
Sudden infant death and lysinuric protein intoleranceJ B de Klerk, M Duran, J G Huijmans, et al.
Tijdschrift Voor Kindergeneeskunde|December 1, 1987
[Reye's syndrome]M Berghuis, A J van Vught, J B de Klerk, et al.
Journal of Inherited Metabolic Disease|January 1, 1984
The differential diagnosis of dicarboxylic aciduriaM Duran, J B De Klerk, S K Wadman, et al.
Clinical Chemistry|March 1, 1988
Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiencyM Duran, L Bruinvis, D Ketting, et al.
Neuropediatrics|May 1, 1990
Quasi-moyamoya disease and heterozygosity for homocystinuria in a five-year-old girlR van Diemen-Steenvoorde, O van Nieuwenhuizen, J B de Klerk, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Maternal PKU syndrome in an exceptional family with unexpected PKUJ B De Klerk, S K Wadman, H J Dijkhuis, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyH Przyrembel, C Jakobs, L IJlst, et al.
Journal of Inherited Metabolic Disease|January 1, 1991
Octanoate and palmitate beta-oxidation in human leukocytes: implications for the rapid diagnosis of fatty acid beta-oxidation disordersR J Wanders, L Ijlst, E van Elk, et al.
Archives of Dermatology|September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant ricketsA P Oranje, H Przyrembel, M Meradji, et al.
Pageof 5