G. P. A. Smit - Concepedia

Author

G. P. A. Smit

University of Groningen

Also Known As

G P A Smit, G P Smit, G. P. A. Smit, G. Peter A. Smit, G. Smit, G.P.A. Smit, GPA Smit, Smit, G. P. A.

Publications

897

Citations

H-Index

Concepts

All Affiliations

University of Groningen University of Amsterdam Beatrix Kinderziekenhuis Radboud University Nijmegen Erasmus MC - Sophia Children’s Hospital

About

G. P. A. Smit is an author at University of Groningen specializing in medicine, inherited metabolic disease, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	295
2	Hepatology	2	2	107
3	Metabolism	2	2	116
4	Emergency Medicine	1	1	27
5	Immunology	1	1	72

G. P. A. Smit

Publications

694

Citations

H-Index

Page 1

	Year	Citations
Impaired prenatal and postnatal growth in Dutch patients with phenylketonuria. The National PKU Steering Committee. P.H. Verkerk, F. J. van Spronsen, G. P. A. Smit, Archives of Disease in Childhood	1994	84
Mevalonic aciduria: an inborn error of cholesterol biosynthesis? Rolf M.F. Berger, G. P. A. Smit, Henk H. Schierbeek, Clinica Chimica Acta OxysterolPathologyMevalonic AciduriaHyperlipidemiaMetabolomics	1985	81
Absence of hepatic molybdenum cofactor: An inborn error of metabolism leading to a combined deficiency of sulphite oxidase and xanthine dehydrogenase S.K. Wadman, M. Durán, F. A. Beemer, Journal of Inherited Metabolic Disease	1983	76
Type Iiib Glycogen Storage Disease Associated With End–Stage Cirrhosis and Hepatocellular Carcinoma E. B. Haagsma, G. P. A. Smit, Klary E. Niezen‐Koning, Hepatology TransplantationHepatologyGsd Subtype IiibLiver PhysiologyImmunology	1997	72
Identification and Characterization of Three Novel Missense Mutations in Mevalonate Kinase cDNA Causing Mevalonic Aciduria, a Disorder of Isoprene Biosynthesis Sander M. Houten, G. J. Romeijn, Janet Koster, Human Molecular Genetics	1999	64
Neonatal screening for medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency in The Netherlands: The importance of enzyme analysis to ascertain true MCAD deficiency Terry G. J. Derks, Theo Boer, Arend van Assen, Journal of Inherited Metabolic Disease	2008	58
Age-related accumulation of phytanic acid in plasma from patients with the cerebro-hepato-renal (Zellweger) syndrome Ronald J. A. Wanders, Watske Smit, H. S. A. Heymans, Clinica Chimica Acta Phytanic AcidRenal FunctionHepatologyMedicineAge-related Accumulation	1987	35
A patient with lethal cardiomyopathy and a carnitine — acylcarnitine translocase deficiency Klary E. Niezen‐Koning, F. J. van Spronsen, Lodewijk IJlst, Journal of Inherited Metabolic Disease MedicineCardiologyLethal Cardiomyopathy	1995	33
Does impaired growth of PKU patients correlate with the strictness of dietary treatment? FJ van Spronsen, PH Verkerk, Mark van Houten, Acta Paediatrica	1997	30
NPT4, a new microsomal phosphate transporter: Mutation analysis in glycogen storage disease type Ic Daniela Melis, Adrie C. Havelaar, Elly Verbeek, Journal of Inherited Metabolic Disease	2004	28

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