H. S. A. Heymans - Concepedia

Author

H. S. A. Heymans

Also Known As

H Heymans, H S A Heymans, H S Heymans, H SA Heymans, H. Heymans, H. S. A. HEYMANS, H. S. A. Heymans, H. S. Heymans, H. S.A. Heymans, H.S.A. Heymans

200

Publications

9.3K

Citations

H-Index

141

Concepts

All Affiliations

University of Amsterdam Amsterdam UMC Location University of Amsterdam Emma Kinderziekenhuis Utrecht University University of Groningen

About

H. S. A. Heymans is an author at University of Amsterdam specializing in medicine, pathology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	29	41	3.1K
2	Health Sciences	9	9	1.1K
3	Public Health	5	5	282
4	Natural Sciences	2	2	186
5	Anatomy	1	1	61

H. S. A. Heymans

Publications

6.6K

Citations

H-Index

Page 1

	Year	Citations
Mortality and causes of death of end-stage renal disease in children: A Dutch cohort study Jaap W. Groothoff, Mariken Gruppen, Martin Offringa, Kidney International GlomerulonephritisHemodialysisUrologyRenal DiseaseRenal Function	2002	377
Severe plasmalogen deficiency in tissues of infants without peroxisomes (Zellweger syndrome) H. S. A. Heymans, R. B. H. Schutgens, Raymond K. Tan, Nature Severe Plasmalogen DeficiencyPhysiologyHematologyPediatricsInherited Metabolic Disease	1983	348
Human peroxisomal 3-oxoacyl-coenzyme A thiolase deficiency. A. W. Schram, Sidney Goldfischer, C W van Roermund, Proceedings of the National Academy of Sciences Lipid PeroxidationFatty Liver DiseaseRedox BiologyA Thiolase DeficiencyOxidative Stress	1987	203
Activity of peroxisomal enzymes and intracellular distribution of catalase in Zellweger syndrome Ronald J. A. Wanders, Milan Kos, B.C. Roest, Biochemical and Biophysical Research Communications Peroxisomal EnzymesCellular EnzymologyBiochemistryPhysiologyBiochemical Genetics	1984	200
Defining chronic diseases and health conditions in childhood (0–18 years of age): national consensus in the Netherlands Lidwine B. Mokkink, Johanna H. van der Lee, Martha A. Grootenhuis, European Journal of Pediatrics DiagnosisNon-communicable DiseaseAdolescent Chronic IllnessAdolescent MedicinePediatric Epidemiology	2008	198
Hidden Consequences of Success in Pediatrics: Parental Health-Related Quality of Life—Results From the Care Project Janneke Hatzmann, H. S. A. Heymans, Ada Ferrer‐i‐Carbonell, PEDIATRICS	2008	196
Deficiency of acyl-CoA: Dihydroxyacetone phosphate acyltransferase in patients with Zellweger (cerebro-hepato-renal) syndrome R. B. H. Schutgens, G.J. Romeyn, Ronald J. A. Wanders, Biochemical and Biophysical Research Communications HepatologyBiochemistryInherited Metabolic DiseaseIga GlomerulonephritisDihydroxyacetone Phosphate Acyltransferase	1984	193
Hereditary Tyrosinemia Type I: A New Clinical Classification With Difference in Prognosis on Dietary Treatment Francjan J. van Spronsen, Yolande Thomasse, Peter Smit, Hepatology New Clinical ClassificationTyrosinemia TypeDisease ProgressionPrognosisGenetic Epidemiology	1994	192
Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency: Clinical Presentation and Follow-Up of 50 Patients M. E. J. den Boer, Ronald J. A. Wanders, Andrew A. M. Morris, PEDIATRICS	2002	189
Intestinal permeability in patients with coeliac disease and relatives of patients with coeliac disease. Ruurd M. van Elburg, J J Uil, Chris J. Mulder, Gut NutritionIntestinal PermeabilityFood IntoleranceFunctional Gastrointestinal DisorderCoeliac Disease	1993	179

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