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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.
Tijdschrift Voor Kindergeneeskunde
|
December 1, 1987
[Reye's syndrome]
M Berghuis, A J van Vught, J B de Klerk, et al.
Neuropediatrics
|
May 1, 1990
Quasi-moyamoya disease and heterozygosity for homocystinuria in a five-year-old girl
R van Diemen-Steenvoorde, O van Nieuwenhuizen, J B de Klerk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
The differential diagnosis of dicarboxylic aciduria
M 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 deficiency
M Duran, L Bruinvis, D Ketting, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Maternal PKU syndrome in an exceptional family with unexpected PKU
J B De Klerk, S K Wadman, H J Dijkhuis, et al.
Archives of Dermatology
|
September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets
A P Oranje, H Przyrembel, M Meradji, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial beta-oxidation defects
W Onkenhout, V Venizelos, H R Scholte, et al.
Pediatrics
|
September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment
J G Huijmans, M Duran, J B de Klerk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolism
M Coker, J B de Klerk, B T Poll-The, et al.
Page
of 4
Search research articles
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Showing results (1-10 of 35) with videos related to
Sort By:
Page
of 4
Tijdschrift Voor Kindergeneeskunde
|
June 1, 1983
[A patient with neonatal citrullinemia]
M Berghuis, B P Cats, J B de Klerk, et al.
Tijdschrift Voor Kindergeneeskunde
|
December 1, 1987
[Reye's syndrome]
M Berghuis, A J van Vught, J B de Klerk, et al.
Neuropediatrics
|
May 1, 1990
Quasi-moyamoya disease and heterozygosity for homocystinuria in a five-year-old girl
R van Diemen-Steenvoorde, O van Nieuwenhuizen, J B de Klerk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1984
The differential diagnosis of dicarboxylic aciduria
M 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 deficiency
M Duran, L Bruinvis, D Ketting, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1987
Maternal PKU syndrome in an exceptional family with unexpected PKU
J B De Klerk, S K Wadman, H J Dijkhuis, et al.
Archives of Dermatology
|
September 1, 1994
Solomon's epidermal nevus syndrome (type: linear nevus sebaceus) and hypophosphatemic vitamin D-resistant rickets
A P Oranje, H Przyrembel, M Meradji, et al.
Journal of Inherited Metabolic Disease
|
August 7, 2001
Intermediates of unsaturated fatty acid oxidation are incorporated in triglycerides but not in phospholipids in tissues from patients with mitochondrial beta-oxidation defects
W Onkenhout, V Venizelos, H R Scholte, et al.
Pediatrics
|
September 2, 2000
Functional hyperactivity of hepatic glutamate dehydrogenase as a cause of the hyperinsulinism/hyperammonemia syndrome: effect of treatment
J G Huijmans, M Duran, J B de Klerk, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1996
Plasma total odd-chain fatty acids in the monitoring of disorders of propionate, methylmalonate and biotin metabolism
M Coker, J B de Klerk, B T Poll-The, et al.
Page
of 4