O.F. Brouwer - Concepedia

Author

O.F. Brouwer

University Medical Center Groningen

Also Known As

O F BROUWER, O F Brouwer, O F brouwer, O. Brouwer, O. F. Brouwer, O.F. Brouwer, OF Brouwer

Publications

748

Citations

H-Index

Concepts

All Affiliations

University Medical Center Groningen University of Groningen Leiden University Beatrix Kinderziekenhuis Leiden University Medical Center

About

O.F. Brouwer is an author at University Medical Center Groningen specializing in medicine, neurology, and neuropsychology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	258
2	Social Sciences	4	4	139
3	Health Sciences	3	3	74
4	Anatomy	1	1	25
5	Child Development	1	1	46

O.F. Brouwer

Publications

511

Citations

H-Index

Page 1

	Year	Citations
Seizure Severity in Children with Epilepsy: A Parent‐Completed Scale Compared with Clinical Data Johannes A. Carpay, J. Vermuelen, Hans Stroink, Epilepsia	1997	56
Spasticity, dyskinesia and ataxia in cerebral palsy: Are we sure we can differentiate them? Hendriekje Eggink, Daan Kremer, O.F. Brouwer, European Journal of Paediatric Neurology NeurorehabilitationNeuropsychologyCorticobasal DegenerationNeurological DisorderDiagnosis	2017	55
Burst suppression on amplitude‐integrated electroencephalogram may be induced by midazolam: a report on three cases HJ ter Horst, O.F. Brouwer, AF Bos Acta Paediatrica	2004	49
Subjective sleep disturbances in children with partial epilepsy and their effects on quality of life Th. Gutter, O.F. Brouwer, A.W. de Weerd Epilepsy & Behavior Sleep DisordersSleepNeuropsychologySleep DisorderNeuropsychological Functioning	2013	46
Cerebral Vasculopathy Associated With Primary Varicella Infection J.F.V. Caekebeke, A.C.B. Peters, Bodvar Vandvik, Archives of Neurology VaricesAcute Childhood HemiplegiaVasculitisMedicinePathogenesis	1990	46
A homozygous <i>FKRP</i> start codon mutation is associated with Walker–Warburg syndrome, the severe end of the clinical spectrum J. van Reeuwijk, MJW Olderode‐Berends, Christa van den Elzen, Clinical Genetics	2010	42
A novel mutation in MED12 causes FG syndrome (Opitz-Kaveggia syndrome) Patrick Rump, RC Niessen, KT Verbruggen, Clinical Genetics	2010	33
Movement analysis in neonates with spina bifida aperta Deborah A. Sival, O.F. Brouwer, Janneke L.M. Bruggink, Early Human Development NeonatologyPediatricsMotor ControlPrenatal DiagnosisHuman Movement	2005	32
[Deliberate termination of life in newborns in The Netherlands; review of all 22 reported cases between 1997 and 2004]. Eduard Verhagen, Jeanine J. Sol, O.F. Brouwer, PubMed	2005	31
Refinement of the chromosome 16 locus for benign familial infantile convulsions EH Van Den Boogerd, I.F.M. de Coo, R. ten Houten, Clinical Genetics Down SyndromePartial Epilepsy SyndromeDevelopmental AnomalyMendelian DisorderCytogenetics	2005	30

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