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Browsing by Author Gabreëls, F.J.M.

Full Text	Issue Date	Title	Author(s)
	2011	Comparison of 3 instruments to measure muscle strength in children: A prospective study	Beld, W.A. van den; Sanden, G.A. van der; Janssen, A.J.W.M.; Sengers, R.C.A.; Verbeek, A.L.M., et al
	2010	Antihypertensive treatment during pregnancy and functional development at primary school age in a historical cohort study.	Pasker-de Jong, P.C.M.; Zielhuis, G.A.; Gelder, M.M.H.J. van; Pellegrino, A.; Gabreëls, F.J.M., et al
	2006	Distal spinal muscular atrophy as a major feature in adult-onset ataxia telangiectasia.	Hiel, J.A.P.; Engelen, B.G.M. van; Weemaes, C.M.R.; Broeks, A.; Verrips, A., et al
	2006	Validity and reproducibility of the Jamar dynamometer in children aged 4-11 years.	Beld, W.A. van den; Sanden, G.A. van der; Sengers, R.C.A.; Verbeek, A.L.M.; Gabreëls, F.J.M.
	2006	Validity and reproducibility of a new diagnostic motor performance test in children with suspected myopathy.	Beld, W.A. van den; Sanden, G.A. van der; Sengers, R.C.A.; Verbeek, A.L.M.; Gabreëls, F.J.M.
	2006	Fragmented visuospatial processing in children with pervasive developmental disorder.	Schlooz, W.A.; Hulstijn, W.; Broek, P.J.J.A. van den; Pijll, A.C.A.M. van der; Gabreëls, F.J.M., et al
	2006	Validity and reproducibility of hand-held dynamometry in children aged 4-11 years.	Beld, W.A. van den; Sanden, G.A. van der; Sengers, R.C.A.; Verbeek, A.L.M.; Gabreëls, F.J.M.
	2006	A new motor performance test in a prospective study on children with suspected myopathy.	Beld, W.A. van den; Sanden, G.A. van der; Feuth, A.B.; Janssen, A.J.M.; Sengers, R.C.A., et al
	2005	Histology of hereditary neuralgic amyotrophy.	Alfen, N. van; Gabreëls-Festen, A.A.W.M.; Laak, H.J. ter; Arts, W.F.M.; Gabreëls, F.J.M., et al
	2004	MR imaging and proton MR spectroscopic studies in Sjogren-Larsson syndrome: characterization of the leukoencephalopathy.	Willemsen, M.A.A.P.; Graaf, M. van der; Knaap, M.S. van der; Heerschap, A.; Domburg, P.H.M.F. van, et al
	2004	Effect of botulinum toxin in the treatment of drooling: a controlled clinical trial.	Jongerius, P.H.; Hoogen, F.J.A. van den; Limbeek, J. van; Gabreëls, F.J.M.; Hulst, K. van, et al
	2004	Botulinum toxin effect on salivary flow rate in children with cerebral palsy.	Jongerius, P.H.; Rotteveel, J.J.; Limbeek, J. van; Gabreëls, F.J.M.; Hulst, K. van, et al
	1998	Infantile motor neuron disease with autonomic dysfunction and bunina bodies	Semmekrot, B.A.; Wesseling, P.; Bruinenberg, J.F.M.; Gabreëls, F.J.M.; Laak, H.J. ter, et al
	1997	Clinical heterogenity in respiratory chain complex III deficiency in childhood	Mourmans, J.; Wendel, U.A.H.; Bentlage, H.A.C.M.; Trijbels, J.M.F.; Smeitink, J.A.M., et al
	1997	The clinical phenotype of succinic semialdehyde dehydrogenase deficiency (4-Hydroxybutyric Aciduria): case reports of 23 new patients	Gibson, K.M.; Christensen, E.; Jakobs, C.; Fowler, B.; Clarke, M.A., et al
	1997	Multicore myopathy with restrictive cardiomyopathy	Willemsen, M.A.A.P.; Oort, A.M. van; Laak, H.J. ter; Sengers, R.C.A.; Gabreëls, F.J.M.
	1997	Exon skipping in the sterol 27-hydroxylase gene leads to cerebrotendinous xanthomatosis	Verrips, A.; Steenbergen-Spanjers, G.C.H.; Luyten, J.A.F.M.; Wevers, R.A.; Wokke, J.H.J., et al
	1997	Towards a standardised assessment procedure for developmental apraxia of speech	Thoonen, G.H.J.; Maassen, B.A.M.; Gabreëls, F.J.M.; Schreuder, R.; Swart, B.J.M. de
	1997	A new leukoencephalopathy with vanishing white matter	Knaap, M.S. van der; Barth, P.G.; Gabreëls, F.J.M.; Franzoni, E.; Begeer, J.H., et al
	1997	Neurodevelopment in offspring of hairdressers	Kersemaekers, W.M.; Roeleveld, N.; Zielhuis, G.A.; Gabreëls, F.J.M.
	1997	Seasonal variation in the prevalence of Down syndrome at birth: a review	Stolwijk, A.M.; Jongbloet, P.H.; Zielhuis, G.A.; Gabreëls, F.J.M.
	1997	Towards a standardised assessment procedure for developmental apraxia of speech	Thoonen, G.H.J.; Maassen, B.A.M.; Gabreëls, F.J.M.; Schreuder, R.; Swart, B.J.M. de
	1997	The aicardi-Goutieres syndrome: variable clinical expression in two siblings	Verrips, A.; Hiel, J.A.P.; Gabreëls, F.J.M.; Wesseling, P.; Rotteveel, J.J.
	1997	Mitochondriële encefalomyopathie, lactaatacidose en stroke-like episodes (MELAS): een zeldzame oorzaak van 'stroke' op jongvolwassen leeftijd	Hiel, J.A.P.; Verrips, A.; Gabreëls, F.J.M.; Keyser, A.; Wesseling, P., et al
	1997	Heterogeneity of Spina Bifida	Blatter, B.M.; Lafeber, A.B.; Peters, P.W.J.; Roeleveld, N.; Verbeek, A.L.M., et al
	1997	The Aicardi-Goutieres syndrome: Variable clinical expression in two siblings	Verrips, A.; Hiel, J.A.P.; Gabreëls, F.J.M.; Wesseling, P.; Rotteveel, J.J.
	1997	Mitochondriële encefalomyopathie, lactaatacidose en stroke-like episodes (melas): een zeldzame oorzaak van "stroke" op jongvolwassen leeftijd	Hiel, J.A.P.; Verrips, A.; Gabreëls, F.J.M.; Keyser, A.J.M.; Wesseling, P., et al
	1996	Two divergent types of nerve pathology in patients with different P0 mutations in Charcot-Marie-Tooth disease	Gabreëls-Festen, A.A.W.M.; Hoogendijk, J.E.; Meijerink, P.H.S.; Gabreëls, F.J.M.; Bolhuis, P.A., et al
	1996	Two divergent types of nerve pathology in patients with different Po mutations in Charcot-Marie-Tooth disease	Gabreëls-Festen, A.A.W.M.; Hoogendijk, J.E.; Meijerink, P.H.S.; Gabreëls, F.J.M.; Bolhuis, P.A., et al
	1996	Mitochondrial cytopathy presenting as hereditary sensory neurophaty 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, I.F.M. de; Ruitenbeek, W., et al
	1996	Association of congenital muscular dystrophy with hypoplasia of the lateral abdominal wall musculature and hypoplasia of the external genitalia	Leyten, Q.H.; Renier, W.O.; Gabreëls, F.J.M.; Brunner, H.G.; Laak, H.J. ter, et al
	1996	Actieve levensbeëindiging bij pasgeborenen met spina bifida?	Rotteveel, J.J.; Mullaart, R.A.; Gabreëls, F.J.M.; Overbeeke, J.J. van
	1996	Isolated case of mental retardation and ataxia due to a de novo mitochondrial T8993G mutation	Coo, I.F.M. de; Smeets, H.J.M.; Gabreëls, F.J.M.; Arts, N.J.M.; Oost, B.A. van
	1996	Toekomstperspectieven voor kinderen met spina bifida aperta	Rotteveel, J.J.; Mullaart, R.A.; Gabreëls, F.J.M.; Overbeeke, J.J. van
	1996	Intestinal pseudo-obstruction syndrom in a child with myotonic dystrophy	Bruinenberg, J.F.M.; Rieu, P.N.M.A.; Gabreëls, F.J.M.; Tolboom, J.J.M.
	1996	Maternal occupational exposure during pregnancy and the risk of spina bifida	Blatter, B.M.; Roeleveld, N.; Zielhuis, G.A.; Gabreëls, F.J.M.; Verbeek, A.L.M.
	1996	Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: an experimental basis for future application in the management of peripheral nerve defect	Wey, L.P. van der; Polder, T.W.; Stegeman, D.F.; Gabreëls-Festen, A.A.W.M.; Spauwen, P.H.M., et al
	1996	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, I.F.M. de; Ruitenbeek, W., et al
	1996	Spina Bifida and parental occupation	Blatter, B.M.; Roeleveld, N.; Zielhuis, G.A.; Mullaart, R.A.; Gabreëls, F.J.M.
	1996	Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: an experimental basis for future application in the management of peripheral nerve defects	Wey, L.P. van der; Spauwen, P.H.M.; Gabreëls, F.J.M.
	1996	Choroid plexus carcinoma: a report of two cases and review of the literature	Geerts, Y.; Gabreëls, F.J.M.; Lippens, R.J.J.; Merx, J.L.; Wesseling, P.
	1996	Spinal muscular atrophy combined with congenital heart disease: a report of two cases	Mulleners, W.M.; Ravenswaay, C.M.A. van; Gabreëls, F.J.M.; Hamel, B.C.J.; Oort, A. van, et al
	1996	Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis	Verrips, A.; Steenbergen-Spanjers, G.C.H.; Luyten, J.A.F.M.; Heuvel, L.P.W.J. van den; Keyser, A., et al
	1996	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, I.F.M. de; Ruitenbeek, W., et al
	1996	Congenital muscular dystrophy: a review of the literature	Leyten, Q.H.; Gabreëls, F.J.M.; Renier, W.O.; Laak, H.J. ter
	1995	Cerebrospinal neuron-specific enolase, S-100 and myelin basic protein in neurological disorders	Lamers, K.J.B.; Engelen, B.G.M. van; Gabreëls, F.J.M.; Hommes, O.R.; Borm, G.F., et al
	1995	Speech motor programming and execution in myothonic dystrophy	Maassen, B.A.M.; Bruggen, J.P. ter; Nanninga-Korver, A.; Spaendonck, K.P.M. van; Weyn Banningh, E.W.A., et al
	1995	Standardized method for high-resolution 1H-NMR of cerebrospinal fluid.	Wevers, R.A.; Engelke, U.F.H.; Wendel, U.A.H.; Jong, J.G.N. de; Gabreëls, F.J.M., et al
	1995	Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency	Hageman, A.T.M.; Gabreëls, F.J.M.; Jong, J.G.N. de; Gabreëls-Festen, A.A.W.M.; Berg, C.J.M.G. van den, et al
	1995	Intramedullary spinal cord abscess	Bartels, R.H.M.A.; Gonera, E.G.; Spek, J.A.N. van der; Thijssen, H.O.M.; Mullaart, R.A., et al