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P. D. Mooy
P. D. Mooy
Erasmus University Rotterdam
Endocrinology
Internal medicine
Biology
Diabetes mellitus
Medicine
5
Papers
59
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Prenatal monitoring for the Hunter syndrome: the heterozygous female fetus.
2008
Clinical Genetics
Wim J. Kleijer
P. D. Mooy
I. Liebaers
J. J. P. van de Kamp
M. F. Niermeijer
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Citations (14)
Defects in Mitochondrial Beta Oxidationa
1986
Annals of the New York Academy of Sciences
H. R. Scholte
I. E. M. Luyt-Houwen
W. Blom
H.F.M. Busch
P.C. Jonge
M. Visser
J. G. M. Huijmans
F.G.I. Jennekens
P. D. Mooy
H. Przyrembel
R.B.H. Schutgens
M. H. M. Vaandrager-Verduin
R.N.A. Coster
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Citations (2)
Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin
1984
European Journal of Pediatrics
P. D. Mooy
H. Przyrembel
M. A. H. Giesberts
H. R. Scholte
W. Blom
H.H. van Gelderen
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Citations (23)
Successful treatment of severe carbamyl phosphate synthetase I deficiency.
1984
Archives of Disease in Childhood
M van de Bor
P. D. Mooy
D. van Zoeren
R. Berger
H.H. van Gelderen
Helena L. Teijema
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Citations (8)
Glutaric Aciduria Type II: Multiple Defects in Isolated Muscle Mitochondria and Deficient β-Oxidation in Fibroblasts
1984
Journal of Inherited Metabolic Disease
P. D. Mooy
M. A. H. Giesberts
H.H. van Gelderen
H. R. Scholte
I. E. M. Luyt-Houwen
H. Przyrembel
W. Blom
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