Results of search for 'au:"Gabreĕls, F J"' › مکتبة رقمیه للعلوم الطبيه catalog

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	181.	Peripheral nerve elongation by laser Doppler flowmetry controlled expansion: morphological aspects. [electronic resource] by van der Wey, L P Gabreëls-Festen, A A Merks, M H Polder, T W Stegeman, D F Spauwen, P H Gabreëls, F J Producer: 19950601 In: Acta neuropathologica vol. 89 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	182.	Argininosuccinic aciduria: clinical and biochemical findings in three children with the late onset form, with special emphasis on cerebrospinal fluid findings of amino acids and pyrimidines. [electronic resource] by Gerrits, G P Gabreëls, F J Monnens, L A De Abreu, R A van Raaij-Selten, B Niezen-Koning, K E Trijbels, J M Producer: 19930518 In: Neuropediatrics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	183.	MECP2 mutation in a boy with severe neonatal encephalopathy: clinical, neuropathological and molecular findings. [electronic resource] by Geerdink, N Rotteveel, J J Lammens, M Sistermans, E A Heikens, G T Gabreëls, F J M Mullaart, R A Hamel, B C J Producer: 20020612 In: Neuropediatrics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	184.	Item assessment in the development of a diagnostic motor performance test for myopathy in children. [electronic resource] by van der Schouw, Y T van den Beld, W A van der Sanden, G A Binkhorst, R A Gabreëls, F J Verbeek, A L Producer: 19980204 In: Developmental medicine and child neurology vol. 35 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	185.	The Martin-Bell syndrome: a psychological, logopaedic and cytogenetic study of two affected brothers. [electronic resource] by Renier, W O Smeets, D F Scheres, J M Hustinx, T W Hulsmans, C F Ophey, C P Bomers, A J Gabreëls, F J Producer: 19830826 In: Journal of mental deficiency research vol. 27 (Pt 1) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	186.	Adult polyglucosan body disease: the diagnostic value of axilla skin biopsy. [electronic resource] by Busard, H L Gabreëls-Festen, A A Renier, W O Gabreëls, F J Joosten, E M van 't Hof, M A Rensing, J B Producer: 19911107 In: Annals of neurology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	187.	Cerebrotendinous xanthomatosis: the spectrum of imaging findings and the correlation with neuropathologic findings. [electronic resource] by Barkhof, F Verrips, A Wesseling, P van Der Knaap, M S van Engelen, B G Gabreëls, F J Keyser, A Wevers, R A Valk, J Producer: 20010111 In: Radiology vol. 217 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	188.	A double missense mutation in the ATM gene of a Dutch family with ataxia telangiectasia. [electronic resource] by van Belzen, M J Hiel, J A Weemaes, C M Gabreëls, F J van Engelen, B G Smeets, D F van den Heuvel, L P Producer: 19980403 In: Human genetics vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	189.	Clinical heterogeneity in respiratory chain complex III deficiency in childhood. [electronic resource] by Mourmans, J Wendel, U Bentlage, H A Trijbels, J M Smeitink, J A de Coo, I F Gabreëls, F J Sengers, R C Ruitenbeek, W Producer: 19970710 In: Journal of the neurological sciences vol. 149 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	190.	Congenital muscular dystrophy and severe central nervous system atrophy in two siblings. [electronic resource] by Leyten, Q H Barth, P G Gabreëls, F J Renkawek, K Renier, W O Gabreëls-Festen, A A ter Laak, H J Smits, M G Producer: 19960605 In: Acta neuropathologica vol. 90 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	191.	Hereditary neuropathy with liability to pressure palsies with a small deletion interrupting the PMP22 gene. [electronic resource] by van de Wetering, R A C Gabreëls-Festen, A A W M Timmerman, V Padberg, G M Gabreëls, F J M Mariman, E C M Producer: 20021213 In: Neuromuscular disorders : NMD vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	192.	Congenital fibre type disproportion. [electronic resource] by ter Laak, H J Jaspar, H H Gabreëls, F J Breuer, T J Sengers, R C Joosten, E M Stadhouders, A M Gabreëls-Festen, A A Producer: 19820120 In: Clinical neurology and neurosurgery vol. 83 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	193.	Clinical symptoms of adult metachromatic leukodystrophy and arylsulfatase A pseudodeficiency. [electronic resource] by Hageman, A T Gabreëls, F J de Jong, J G Gabreëls-Festen, A A van den Berg, C J van Oost, B A Wevers, R A Producer: 19950508 In: Archives of neurology vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	194.	Histology of hereditary neuralgic amyotrophy. [electronic resource] by 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 Producer: 20050315 In: Journal of neurology, neurosurgery, and psychiatry vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	195.	Presence of diarrhea and absence of tendon xanthomas in patients with cerebrotendinous xanthomatosis. [electronic resource] by Verrips, A van Engelen, B G Wevers, R A van Geel, B M Cruysberg, J R van den Heuvel, L P Keyser, A Gabreëls, F J Producer: 20000427 In: Archives of neurology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	196.	Clinical and molecular genetic characteristics of patients with cerebrotendinous xanthomatosis. [electronic resource] by Verrips, A Hoefsloot, L H Steenbergen, G C Theelen, J P Wevers, R A Gabreëls, F J van Engelen, B G van den Heuvel, L P Producer: 20000606 In: Brain : a journal of neurology vol. 123 ( Pt 5) Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	197.	Isolated and combined deficiencies of NADH dehydrogenase (complex I) in muscle tissue of children with mitochondrial myopathies. [electronic resource] by Korenke, G C Bentlage, H A Ruitenbeek, W Sengers, R C Sperl, W Trijbels, J M Gabreels, F J Wijburg, F A Wiedermann, V Hanefeld, F Producer: 19910313 In: European journal of pediatrics vol. 150 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	198.	Reference values for nucleosides and nucleobases in cerebrospinal fluid of children. [electronic resource] by Gerrits, G P Haagen, A A De Abreu, R A Monnens, L A Gabreëls, F J Trijbels, F J Theeuwes, A L van Baal, J M Producer: 19880819 In: Clinical chemistry vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	199.	Congenital adrenal hypoplasia, progressive muscular dystrophy, and severe mental retardation, in association with glycerol kinase deficiency, in male sibs. [electronic resource] by Renier, W O Nabben, F A Hustinx, T W Veerkamp, J H Otten, B J Ter Laak, H J Ter Haar, B G Gabreëls, F J Producer: 19840107 In: Clinical genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	200.	Connatal Pelizaeus-Merzbacher disease with congenital stridor in two maternal cousins. [electronic resource] by Renier, W O Gabreëls, F J Hustinx, T W Jaspar, H H Geelen, J A Van Haelst, U J Lommen, E J Ter Haar, B G Producer: 19810709 In: Acta neuropathologica vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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