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	161.	Reference values of blood components related to fuel metabolism in children after an overnight fast. [electronic resource] by Lamers, K J Doesburg, W H Gabreëls, F J Romsom, A C Renier, W O Wevers, R A Lemmens, W A Producer: 19850515 In: Clinica chimica acta; international journal of clinical chemistry vol. 145 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	162.	Mitochondrial cytopathy presenting as hereditary sensory neuropathy with progressive external ophthalmoplegia, ataxia and fatal myoclonic epileptic status. [electronic resource] by van Domburg, P H Gabreëls-Festen, A A Gabreëls, F J de Coo, R Ruitenbeek, W Wesseling, P ter Laak, H Producer: 19960813 In: Brain : a journal of neurology vol. 119 ( Pt 3) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	163.	Polyglucosan bodies in intramuscular motor nerves. [electronic resource] by Bernsen, R A Busard, H L Ter Laak, H J Gabreëls, F J Renier, W O Joosten, E M Theeuwes, A G Producer: 19890825 In: Acta neuropathologica vol. 77 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	164.	Decreased immunoglobulin class switching in Nijmegen Breakage syndrome due to the DNA repair defect. [electronic resource] by van Engelen, B G Hiel, J A Gabreëls, F J van den Heuvel, L P van Gent, D C Weemaes, C M Producer: 20020308 In: Human immunology vol. 62 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	165.	Two new mutations in the sterol 27-hydroxylase gene in two families lead to cerebrotendinous xanthomatosis. [electronic resource] by Verrips, A Steenbergen-Spanjers, G C Luyten, J A van den Heuvel, L P Keyser, A Gabreëls, F J Wevers, R A Producer: 19970106 In: Human genetics vol. 98 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	166.	Botulinum toxin effect on salivary flow rate in children with cerebral palsy. [electronic resource] by Jongerius, P H Rotteveel, J J van Limbeek, J Gabreëls, F J M van Hulst, K van den Hoogen, F J A Producer: 20060118 In: Neurology vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	167.	Increased cerebrospinal fluid glycine: a biochemical marker for a leukoencephalopathy with vanishing white matter. [electronic resource] by van der Knaap, M S Wevers, R A Kure, S Gabreëls, F J Verhoeven, N M van Raaij-Selten, B Jaeken, J Producer: 20000107 In: Journal of child neurology vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	168.	Lafora disease: a quantitative morphological and biochemical study of the cerebral cortex. [electronic resource] by Busard, H L Renier, W O Gabreëls, F J Jaspar, H H Slooff, J L Janssen, A J Van Haelst, U J Producer: 19870526 In: Clinical neuropathology vol. 6 Availability: No items available. Save to lists Add to cart (remove)
	169.	Polyglucosan bodies in brain tissue: a systematic study. [electronic resource] by Busard, H L Span, J P Renkawek, K Renier, W O Gabreëls, F J Slooff, J L Van 't Hof, M A Producer: 19940714 In: Clinical neuropathology vol. 13 Availability: No items available. Save to lists Add to cart (remove)
	170.	Cerebrotendinous xanthomatosis. Controversies about nerve and muscle: observations in ten patients. [electronic resource] by Verrips, A van Engelen, B G ter Laak, H Gabreëls-Festen, A Janssen, A Zwarts, M Wevers, R A Gabreëls, F J Producer: 20000915 In: Neuromuscular disorders : NMD vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	171.	Reference values for amino acids in cerebrospinal fluid of children determined using ion-exchange chromatography with fluorimetric detection. [electronic resource] by Gerrits, G P Trijbels, F J Monnens, L A Gabreëls, F J De Abreu, R A Theeuwes, A G van Raay-Selten, B Producer: 19890927 In: Clinica chimica acta; international journal of clinical chemistry vol. 182 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	172.	An autosomal dominant type of congenital muscular dystrophy. [electronic resource] by Leyten, Q H Gabreëls, F J Joosten, E M Renier, W O Ter Laak, H J Ter Haar, B G Stadhouders, A M Producer: 19870219 In: Brain & development vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	173.	Progressive idiopathic strio-pallido-dentate calcinosis (Fahr's disease) with autosomal recessive inheritance. Report of three siblings. [electronic resource] by Smits, M G Gabreëls, F J Thijssen, H O 't Lam, R L Notermans, S L ter Haar, B G Prick, J J Producer: 19830623 In: European neurology vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	174.	MELAS syndrome. Report of two patients, and comparison with data of 24 patients derived from the literature. [electronic resource] by van Hellenberg Hubar, J L Gabreëls, F J Ruitenbeek, W Sengers, R C Renier, W O Thijssen, H O ter Laak, H J Producer: 19910701 In: Neuropediatrics vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	175.	Chronic inflammatory demyelinating polyneuropathy in two siblings. [electronic resource] by Gabreëls-Festen, A A Hageman, A T Gabreëls, F J Joosten, E M Renier, W O Weemaes, C M ter Laak, H J Producer: 19860422 In: Journal of neurology, neurosurgery, and psychiatry vol. 49 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	176.	Hereditary neuropathy with liability to pressure palsies: a clinical, electroneurophysiological and morphological study. [electronic resource] by Verhagen, W I Gabreëls-Festen, A A van Wensen, P J Joosten, E M Vingerhoets, H M Gabreëls, F J de Graaf, R Producer: 19930820 In: Journal of the neurological sciences vol. 116 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	177.	A new leukoencephalopathy with vanishing white matter. [electronic resource] by van der Knaap, M S Barth, P G Gabreëls, F J Franzoni, E Begeer, J H Stroink, H Rotteveel, J J Valk, J Producer: 19970515 In: Neurology vol. 48 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	178.	White matter abnormalities in congenital muscular dystrophy. [electronic resource] by Leyten, Q H Gabreëls, F J Renier, W O van Engelen, B G ter Laak, H J Sengers, R C Thijssen, H O Producer: 19950815 In: Journal of the neurological sciences vol. 129 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	179.	Biochemical hallmarks of tyrosine hydroxylase deficiency. [electronic resource] by Bräutigam, C Wevers, R A Jansen, R J Smeitink, J A de Rijk-van Andel, J F Gabreëls, F J Hoffmann, G F Producer: 19980916 In: Clinical chemistry vol. 44 Availability: No items available. Save to lists Add to cart (remove)
	180.	Cognitive function in early adult and adult onset myotonic dystrophy. [electronic resource] by Van Spaendonck, K P Ter Bruggen, J P Weyn Banningh, E W Maassen, B A Van de Biezenbos, J B Gabreëls, F J Producer: 19951026 In: Acta neurologica Scandinavica vol. 91 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 229 results.