Adenylosuccinase deficiency: an inborn error of purine nucleotide synthesis
J Jaeken, SK Wadman, M Duran… - European journal of …, 1988 - Springer
Clinical and biochemical data are presented on eight children with adenylosuccinase
deficiency. This newly discovered inborn error of purine metabolism is characterized by an …
deficiency. This newly discovered inborn error of purine metabolism is characterized by an …
3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of …
M Duran, RJA Wanders, JP De Jager, L Dorland… - European journal of …, 1991 - Springer
Two siblings were found to be affected by longchain 3-hydroxyacyl-CoA dehydrogenase
deficiency, one of which died suddenly and unexpectedly on the 3rd day of life suffering from …
deficiency, one of which died suddenly and unexpectedly on the 3rd day of life suffering from …
The cerebro‐costo‐mandibular syndrome: third report of familial occurrence
RCM Hennekam, FA Beemer, WAR Huijbers… - Clinical …, 1985 - Wiley Online Library
The cerebroâ•’costoâ•’mandibular syndrome: third report of familial occurrence Page 1 C'linicul
Geneticr 1985: 28: 118 121 The cerebro-costo-mandibular syndrome: third report of familial …
Geneticr 1985: 28: 118 121 The cerebro-costo-mandibular syndrome: third report of familial …
Computer analysis of the EEG as an aid in terminating diet therapy in phenylketonuria
DN Donker, D Reits, W Storm Van Leeuwen… - Revue D' …, 1978 - europepmc.org
In 6 patients with PKU, being on a low phenylalanine diet, the effect of reintroduction of
phenylalanine on the EEG was studied. The children, therefore, received daily loads of 100 or …
phenylalanine on the EEG was studied. The children, therefore, received daily loads of 100 or …
[CITAAT][C] Three new cases of histidinemia: Clinical and biochemical data
SK Wadman, FJVAN SPRANG… - Acta …, 1967 - Wiley Online Library
A girl (M. t. B.) born July 7th, 1957, was the third child of healthy parents. The first child, a boy,
was still-born; the second one, a girl, is normal. The patient was born after a normal …
was still-born; the second one, a girl, is normal. The patient was born after a normal …
Bacteriological requirements for dried infant and weaning foods. The microbiology of dried foods. Proceedings of the Sixth International Symposium on Food …
FJ Sprang - 1969 - cabidigitallibrary.org
The poor bacteriological quality of some baby foods is commented on. Out of 150 samples
of dried milk used for the preparation of baby food at the Wilhel-mina Children's Hospital, 18% …
of dried milk used for the preparation of baby food at the Wilhel-mina Children's Hospital, 18% …
Tyrosinosis.
HD Bakker, FJ Sprang, SK Wadman - 1976 - cabidigitallibrary.org
The chemistry of tyrosine metabolism and the involvement of p-hydroxyphenylpyruvate
hydroxylase (EC 1.99.1.14) in the disturbance of metabolism in tyrosinosis are briefly reviewed. …
hydroxylase (EC 1.99.1.14) in the disturbance of metabolism in tyrosinosis are briefly reviewed. …
The significance of milk for the treatment of some inborn errors of metabolism.
FJV Sprang - 1964 - cabidigitallibrary.org
The rôle of milk in galactosaemia and phenyl-ketonuria is discussed. In the former, traces of
milk are toxic while in the latter, small amounts of milk in the diet are desirable for normal …
milk are toxic while in the latter, small amounts of milk in the diet are desirable for normal …
[CITAAT][C] Methylmalonic acidaemia. Experience of diagnosis and treatment in some patients.
HD Bakker, M Duran, AH Gennip, FJ Sprang… - 1978 - cabidigitallibrary.org
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[CITAAT][C] Microbiological quality assurance for weaning formulae
DAA Mossel, GA Harrewijn, FJ Van Sprang - International Symposium on Food …, 1973