F. Gabreëls
Univé (Netherlands)(NL)
Publications by Year
Research Areas
Hereditary Neurological Disorders, Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, Language Development and Disorders, Neurogenetic and Muscular Disorders Research
Most-Cited Works
- → A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects?(1998)1,559 cited
- → Complex regional pain syndrome type I (RSD)(1998)186 cited
- → Coarticulation patterns in children with developmental apraxia of speech(2002)95 cited
- → The integrated use of maximum performance tasks in differential diagnostic evaluations among children with motor speech disorders(1996)90 cited
- → Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression(1999)86 cited
- → 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(1999)85 cited
- → Planning of syllables in children with developmental apraxia of speech(2003)72 cited
- → Towards a standardised assessment procedure for developmental apraxia of speech(1997)63 cited
- → VALIDITY AND REPRODUCIBILITY OF HAND-HELD DYNAMOMETRY IN CHILDREN AGED 4–11 YEARS(2005)60 cited
- → Hereditary Demyelinating Motor and Sensory Neuropathy(1993)59 cited