F. Gabreëls - Concepedia

Author

F. Gabreëls

Also Known As

F Gabreels, F Gabreëls, F. Gabreels, F. Gabreëls, F. Gabreëls, F. Gabre�ls, F. M. Gabreëls, F.J.M. Gabreëls, Fons Gabreels, Fons Gabreëls

Publications

2.9K

Citations

H-Index

Concepts

All Affiliations

Radboud University Nijmegen Radboud University Medical Center Max Planck Institute for Psycholinguistics Wilhelmina Children's Hospital

About

F. Gabreëls is an author at Radboud University Nijmegen specializing in medicine, neuroanatomy, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	10	10	1.8K
2	Health Sciences	4	4	213
3	Arts	1	1	90
4	Education	1	1	37
5	Language Studies	1	1	44

F. Gabreëls

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? N.M.J. van der Put, F. Gabreëls, E M Stevens, The American Journal of Human Genetics Developmental BiologySecond Common MutationNeural-tube DefectsGenetic DisorderMendelian Disorder	1998	1.6K
Complex regional pain syndrome type I (RSD) Lijckle van der Laan, H. J. ter Laak, Anneke Gabreëls-Festen, Neurology	1998	186
Coarticulation patterns in children with developmental apraxia of speech Lian Nijland, Ben Maassen, Sjoeke van der Meulen, Clinical Linguistics & Phonetics	2002	95
The integrated use of maximum performance tasks in differential diagnostic evaluations among children with motor speech disorders Geert Thoonen, Ben Maassen, J. Wit, Clinical Linguistics & Phonetics Articulation (Speech Science)Language DevelopmentPathological SpeechAcquired Apraxia Of SpeechSpeech Sound Disorder	1996	90
Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression Ineke van der Burgt, Geert Thoonen, Natasja Roosenboom, The Journal of Pediatrics Intellectual ImpairmentChild PsychologyCognitive ScienceNeuropsychologyNeuropsychological Functioning	1999	86
Study on the gene and phenotypic characterisation of autosomal recessive demyelinating motor and sensory neuropathy (Charcot-Marie-Tooth disease) with a gene locus on chromosome 5q23-q33 A.A.W.M. Gabreëls‐Festen, Sylvia E. C. van Beersum, L. Eshuis, Journal of Neurology Neurosurgery & Psychiatry	1999	85
Planning of syllables in children with developmental apraxia of speech Lian Nijland, Ben Maassen, Sjoeke van der Meulen, Clinical Linguistics & Phonetics	2003	72
Towards a standardised assessment procedure for developmental apraxia of speech Geert Thoonen, Ben Maassen, F. Gabreëls, International Journal of Language & Communication Disorders	1997	63
VALIDITY AND REPRODUCIBILITY OF HAND-HELD DYNAMOMETRY IN CHILDREN AGED 4–11 YEARS Willeke van den Beld, R. C. A. Sengers, André L. M. Verbeek, Journal of Rehabilitation Medicine	2005	60
Pyruvate dehydrogenase deficiency restricted to brain M.J.J. Prick, F. Gabreëls, W.O. Renier, Neurology	1981	50

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