Carine I. van Capelle

Author

Erasmus MC ORCID

Also Known As

C. I. van Capelle, C.I. Van Capelle, C.I. van Capelle, Carine I. van Capelle, Carine van Capelle

Publications

1.5K

Citations

H-Index

Concepts

All Affiliations

Erasmus MC Erasmus MC - Sophia Children’s Hospital Erasmus University Rotterdam Radboud University Nijmegen Radboud University Medical Center

About

Carine I. van Capelle is an author at Erasmus MC specializing in medicine, pediatrics, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	424
2	Public Health	3	3	190
3	Neurology	2	2	126
4	Arts	1	1	89
5	Epidemiology	1	1	99

Carine I. van Capelle

Publications

1.5K

Citations

H-Index

Page 1

	Year	Citations
A Randomized Study of Alglucosidase Alfa in Late-Onset Pompe's Disease Ans T. van der Ploeg, Paula R. Clemens, Deyanira Corzo, New England Journal of Medicine	2010	726
Rate of progression and predictive factors for pulmonary outcome in children and adults with Pompe disease Nadine A. M. E. van der Beek, Carine I. van Capelle, K.I. van der Velden-van Etten, Molecular Genetics and Metabolism Pompe DiseaseEpidemiologyAdvanced Lung DiseasePredictive FactorsClinical Epidemiology	2011	99
Eight years experience with enzyme replacement therapy in two children and one adult with Pompe disease Carine I. van Capelle, Léon P. F. Winkel, M.L.C. Hagemans, Neuromuscular Disorders Pompe DiseaseEnzyme Replacement TherapyInherited Metabolic DiseasePediatricsSubstrate Reduction Therapy	2008	98
Facial‐muscle weakness, speech disorders and dysphagia are common in patients with classic infantile Pompe disease treated with enzyme therapy Carin M. Van Gelder, Carine I. van Capelle, Berendine J. Ebbink, Journal of Inherited Metabolic Disease Enzyme TherapyMotor DevelopmentOtorhinolaryngologySpeech Sound DisorderSpeech Disorders	2011	89
Childhood Pompe disease: clinical spectrum and genotype in 31 patients Carine I. van Capelle, Jan C. van der Meijden, Johanna M. P. van den Hout, Orphanet Journal of Rare Diseases	2016	63
The quick motor function test: a new tool to rate clinical severity and motor function in Pompe patients Carine I. van Capelle, Nadine A. M. E. van der Beek, Juna M. de Vries, Journal of Inherited Metabolic Disease	2011	62
Hearing loss in Pompe disease revisited: results from a study of 24 children Carine I. van Capelle, André Goedegebure, Nienke C. Homans, Journal of Inherited Metabolic Disease	2010	60
Effect of enzyme therapy in juvenile patients with Pompe disease: A three-year open-label study Carine I. van Capelle, Nadine A. M. E. van der Beek, M.L.C. Hagemans, Neuromuscular Disorders Pompe DiseasePediatric EpidemiologyEnzyme TherapyInherited Metabolic DiseaseClinical Epidemiology	2010	58
Cardiac outcome in classic infantile Pompe disease after 13 years of treatment with recombinant human acid alpha-glucosidase Carine I. van Capelle, Esther Poelman, Ingrid M.E. Frohn-Mulder, International Journal of Cardiology	2018	41
PAS‐positive lymphocyte vacuoles can be used as diagnostic screening test for Pompe disease M.L.C. Hagemans, Rolinda L. Stigter, Carine I. van Capelle, Journal of Inherited Metabolic Disease	2010	38

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