F.J.M. Gabreëls

Radboud University Nijmegen — Netherlands

Biochemistry, Genetics and Molecular Biology · Life Sciences

51h-index8.4kcitations245works0.02yr avg
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Research Topics

Metabolism and Genetic Disorders(47), Mitochondrial Function and Pathology(46), Genetic Neurodegenerative Diseases(26), Hereditary Neurological Disorders(25), Muscle Physiology and Disorders(18)

Publications245 total

Antihypertensive Treatment During Pregnancy and Functional Development at Primary School Age in a Historical Cohort Study
Obstetric Anesthesia Digest·2011· 5 cited
Comparison of 3 instruments to measure muscle strength in children: A prospective study
European Journal of Paediatric Neurology·2011· 19 cited
Building centres of expertise according to the Dutch model?
Orphanet Journal of Rare Diseases·2010· 35 citedOpen Access
Subacute necrotizing encephalomyelopathy (Leigh syndrome) associated with disturbed oxidation of pyruvate, malate and 2-oxoglutarate in muscle and liver
Acta Neurologica Scandinavica·2009· 39 cited
Cognitive function in early adult and adult onset myotonic dystrophy
Acta Neurologica Scandinavica·2009· 27 cited
Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders
Acta Neurologica Scandinavica·2009· 126 cited
Defects in citric acid cycle and the electron transport chain in progressive poliodystrophy
Acta Neurologica Scandinavica·2009· 31 cited
Muscle Reflexes and Synergies Triggered by an Unexpected Support Surface Height During Walking
Journal of Neurophysiology·2007· 98 cited
new motor performance test in a prospective study on children with suspected myopathy
Developmental Medicine & Child Neurology·2007Open Access
A new motor performance test in a prospective study on children with suspected myopathy
Developmental Medicine & Child Neurology·2006· 10 cited
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia
Neurology·2006· 37 cited
Validity and reproducibility of the Jamar dynamometer in children aged 4 – 11 years
Disability and Rehabilitation·2006· 52 cited
Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy
Developmental Medicine & Child Neurology·2005· 14 cited
Botulinum toxin effect on salivary flow rate in children with cerebral palsy
Neurology·2004· 94 cited
Effect of Botulinum Toxin in the Treatment of Drooling: A Controlled Clinical Trial
PEDIATRICS·2004· 201 citedOpen Access
MR imaging and proton MR spectroscopic studies in Sjögren-Larsson syndrome: characterization of the leukoencephalopathy.
PubMed·2004· 88 citedOpen Access
Nijmegen Breakage Syndrome: A Neuropathological Study
Neuropediatrics·2003· 14 cited
The Treatment of Drooling by Ultrasound‐Guided Intraglandular Injections of Botulinum Toxin Type A Into the Salivary Glands
The Laryngoscope·2003· 125 cited
Diagnosis and Differential Diagnosis of Muscle Cramps: A Clinical Approach
Journal of Clinical Neuromuscular Disease·2002· 19 cited
Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene
Neuromuscular Disorders·2002· 27 cited
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Frequent Co-authors

Ron A. Wevers(11), Baziel G.M. van Engelen(8), A.A.W.M. Gabreëls‐Festen(8), Jan J. Rotteveel(7), W. Ruitenbeek(5), Aad Verrips(5), R. C. A. Sengers(5), E.M.G. Joosten(5), Marjo S. van der Knaap(4), Frank J. A. van den Hoogen(3), A. Keyser(3), W.O. Renier(3), Pieter A. Bolhuis(3), W.O. Renier(3), Jan Smeıtınk(3), Arend Heerschap(3), F.G.I. Jennekens(3), P.J.E. Poels(2), Bernard A. van Oost(2), Lambert P.W.J. van den Heuvel(2)