M. Sinaasappel - Concepedia

Author

M. Sinaasappel

Erasmus MC - Sophia Children’s Hospital

Also Known As

M Sinaasappel, M. SINAASAPPEL, M. Sinaasappel, MAARTEN SINAASAPPEL, Maarten Sinaasappel

110

Publications

3.1K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC - Sophia Children’s Hospital Erasmus University Rotterdam Erasmus MC Amsterdam UMC Location University of Amsterdam Wilhelmina Children's Hospital

About

M. Sinaasappel is an author at Erasmus MC - Sophia Children’s Hospital specializing in medicine, pathology, and physiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	863
2	Health Sciences	4	4	125
3	Public Health	2	2	198
4	Education	1	1	10
5	Nursing	1	1	171

M. Sinaasappel

Publications

2.1K

Citations

H-Index

Page 1

	Year	Citations
Defining DIOS and Constipation in Cystic Fibrosis With a Multicentre Study on the Incidence, Characteristics, and Treatment of DIOS Roderick H.J. Houwen, Hubert P. J. van der Doef, Isabelle Sermet‐Gaudelus, Journal of Pediatric Gastroenterology and Nutrition	2009	191
Current Therapy for Crigler–Najjar Syndrome Type 1: Report of A World Registry C N van der Veere, M. Sinaasappel, Antony F. McDonagh, Hepatology	1996	172
When is a coeliac a coeliac? Report of a working group of the United European Gastroenterology Week in Amsterdam, 2001 Carlo Catassi, Christophe Cellier, Nadine Cerf–Bensussan, European Journal of Gastroenterology & Hepatology Evidence-based MedicineGastroenterologyClinical PresentationClinical GuidelinesSurgery	2001	171
Changes in Globus Pallidus With (Pre)Term Kernicterus Paul Govaert, Maarten H. Lequin, Renate Swarte, PEDIATRICS	2003	160
Determinants of mild clinical symptoms in cystic fibrosis patients. Residual chloride secretion measured in rectal biopsies in relation to the genotype. Henk J. Veeze, Dicky Halley, Jan Bijman, Journal of Clinical Investigation Residual SecretionCystic Fibrosis PatientsPhysiologyGastroenterologyDiagnosis	1994	136
A mutation in bilirubin uridine 5′-diphosphate-glucuronosyltransferase isoform 1 causing Crigler-Najjar syndrome type II Piter J. Bosma, Bart Goldhoorn, Ronald P.J. Oude Elferink, Gastroenterology Mendelian DisorderGenetic DisorderGeneticsPathogenesisInherited Metabolic Disease	1993	101
Gastrointestinal and Other Clinical Manifestations in 17 Children With Congenital Disorders of Glycosylation Type Ia, Ib, and Ic Gerard M. Damen, Hans de Klerk, J. G. M. Huijmans, Journal of Pediatric Gastroenterology and Nutrition	2004	85
Plasmodium falciparum-activated Chloride Channels Are Defective in Erythrocytes from Cystic Fibrosis Patients Patrick Verloo, Clemens H. M. Kocken, Annemarie Voorberg-van der Wel, Journal of Biological Chemistry	2004	82
Birth Prevalence and Survival in Cystic Fibrosis Martijn G. Slieker, Cuno S.P.M. Uiterwaal, M. Sinaasappel, CHEST Journal FibrosisNeonatologyReproductive HealthPediatricsMedicine	2005	70
The differential diagnosis of Crigler—Najjar disease, types 1 and 2, by bile pigment analysis M. Sinaasappel, Peter L. M. Jansen Gastroenterology Bile Pigment AnalysisCrigler—najjar DiseaseBiliary TractDifferential DiagnosisHistopathology	1991	63

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