MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings
Geerdink, N, Rotteveel, J J, Lammens, M, Sistermans, E A, Heikens, G T, Gabreëls, F J M, Mullaart, R A, Hamel, B C J
Published in Neuropediatrics (01.02.2002)
Published in Neuropediatrics (01.02.2002)
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Journal Article
Botulinum toxin effect on salivary flow rate in children with cerebral palsy
Jongerius, P H, Rotteveel, J J, van Limbeek, J, Gabreëls, F J M, van Hulst, K, van den Hoogen, F J A
Published in Neurology (26.10.2004)
Published in Neurology (26.10.2004)
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Journal Article
Nijmegen breakage syndrome: a neuropathological study
Lammens, M, Hiel, J A P, Gabreëls, F J M, van Engelen, B G M, van den Heuvel, L P W J, Weemaes, C M R
Published in Neuropediatrics (01.08.2003)
Published in Neuropediatrics (01.08.2003)
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Journal Article
A systematic review for evidence of efficacy of anticholinergic drugs to treat drooling
Jongerius, P H, van Tiel, P, van Limbeek, J, Gabreëls, F J M, Rotteveel, J J
Published in Archives of Disease in Childhood (01.10.2003)
Published in Archives of Disease in Childhood (01.10.2003)
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Journal Article
Book Review
Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status
Domburg, P. H. M. F. van, Gabreëls-Festen, A. A. W. M., Gabreëls, F. J. M., Coo, R. de, Ruitenbeek, W., Wesseling, P., Laak, H. ter
Published in Brain (London, England : 1878) (01.06.1996)
Published in Brain (London, England : 1878) (01.06.1996)
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Journal Article
Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia
Hiel, J A P, van Engelen, B G M, Weemaes, C M R, Broeks, A, Verrips, A, ter Laak, H, Vingerhoets, H M, van den Heuvel, L P W, Lammens, M, Gabreëls, F J M, Last, J I, Taylor, A M R
Published in Neurology (25.07.2006)
Published in Neurology (25.07.2006)
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Journal Article
Histology of hereditary neuralgic amyotrophy
van Alfen, N, Gabreëls-Festen, A A W M, ter Laak, H J, Arts, W F M, Gabreëls, F J M, van Engelen, B G M
Published in Journal of neurology, neurosurgery and psychiatry (01.03.2005)
Published in Journal of neurology, neurosurgery and psychiatry (01.03.2005)
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Journal Article
Spinal xanthomatosis: a variant of cerebrotendinous xanthomatosis
Verrips, A., Lycklama à Nijeholt, G. J., Barkhof, F., Van Engelen, B. G. M., Wesseling, P., Luyten, J. A. F. M., Wevers, R. A., Stam, J., Wokke, J. H. J., van den Heuvel, L. P. W. J., Keyser, A., Gabreëls, F. J. M.
Published in Brain (London, England : 1878) (01.08.1999)
Published in Brain (London, England : 1878) (01.08.1999)
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Journal Article
Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders
Lamers, K J, van Engelen, B G, Gabreëls, F J, Hommes, O R, Borm, G F, Wevers, R A
Published in Acta neurologica Scandinavica (01.09.1995)
Published in Acta neurologica Scandinavica (01.09.1995)
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Journal Article
A review of biochemical and molecular genetic aspects of tyrosine hydroxylase deficiency including a novel mutation (291delC)
Wevers, R. A., Rijk‐van Andel, J. F., Bräutigam, C., Geurtz, B., Heuvel, L. P. W. J., Steenbergen‐Spanjers, G. C. H., Smeitink, J. A. M., Hoffmann, G. F., Gabreëls, F. J. M.
Published in Journal of inherited metabolic disease (01.06.1999)
Published in Journal of inherited metabolic disease (01.06.1999)
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Journal Article
Conference Proceeding
Idiopathic neuralgic amyotrophy in children. A distinct phenotype compared to the adult form
van Alfen, N, Schuuring, J, van Engelen, B G, Rotteveel, J J, Gabreëls, F J
Published in Neuropediatrics (01.12.2000)
Published in Neuropediatrics (01.12.2000)
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Journal Article
Antihypertensive treatment during pregnancy and functional development at primary school age in a historical cohort study
Pasker‐de Jong, PCM, Zielhuis, GA, van Gelder, MMHJ, Pellegrino, A, Gabreëls, FJM, Eskes, TKAB
Published in BJOG : an international journal of obstetrics and gynaecology (01.08.2010)
Published in BJOG : an international journal of obstetrics and gynaecology (01.08.2010)
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Journal Article
Seasonal variation in the prevalence of Down syndrome at birth: a review
Stolwijk, A M, Jongbloet, P H, Zielhuis, G A, Gabreëls, F J
Published in Journal of Epidemiology & Community Health (01.08.1997)
Published in Journal of Epidemiology & Community Health (01.08.1997)
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Journal Article
Book Review
Scheie syndrome presenting as myopathy
Verrips, A, van Engelen, B G, ter Laak, H, Wesseling, P, de Jong, J, Gabreëls, F J
Published in Neuropediatrics (01.04.2001)
Published in Neuropediatrics (01.04.2001)
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Journal Article
Evidence for genetic heterogeneity underlying hereditary neuropathy with liability to pressure palsies
Mariman, E C, Gabreëls-Festen, A A, van Beersum, S E, Jongen, P J, van de Looij, E, Baas, F, Bolhuis, P A, Ropers, H H, Gabreëls, F J
Published in Human genetics (01.02.1994)
Published in Human genetics (01.02.1994)
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Journal Article
Congenital demyelinating motor and sensory neuropathy with focally folded myelin sheaths
Gabreëls-Festen, A A, Joosten, E M, Gabreëls, F J, Stegeman, D F, Vos, A J, Busch, H F
Published in Brain (London, England : 1878) (01.12.1990)
Published in Brain (London, England : 1878) (01.12.1990)
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Journal Article
Neonatal status convulsivus, spongiform encephalopathy, and low activity of Na+/K(+)-ATPase in the brain
Renkawek, K, Renier, W O, de Pont, J J, Vogels, O J, Gabreëls, F J
Published in Epilepsia (Copenhagen) (01.01.1992)
Published in Epilepsia (Copenhagen) (01.01.1992)
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