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1Academic Journal
المؤلفون: van Karnebeek, C.D.M., van Gelderen, I., Nijhof, G.J., Abeling, N.G., Vreken, P., Redeker, E.J., van Eeghen, A.M., Hoovers, J.M.N., Hennekam, R.C.M.
المصدر: van Karnebeek , C D M , van Gelderen , I , Nijhof , G J , Abeling , N G , Vreken , P , Redeker , E J , van Eeghen , A M , Hoovers , J M N & Hennekam , R C M 2002 , ' An aetiological study of 25 mentally retarded adults with autism ' , Journal of Medical Genetics , vol. 39 , no. 3 , pp. 205-214 . https://doi.org/10.1136/jmg.39.3.205
وصف الملف: application/pdf
Relation: https://dare.uva.nl/personal/pure/en/publications/an-aetiological-study-of-25-mentally-retarded-adults-with-autism(92b993c6-1b93-46f3-9fb9-d96b9c50d3c6).html
الاتاحة: https://dare.uva.nl/personal/pure/en/publications/an-aetiological-study-of-25-mentally-retarded-adults-with-autism(92b993c6-1b93-46f3-9fb9-d96b9c50d3c6).html
https://doi.org/10.1136/jmg.39.3.205
https://pure.uva.nl/ws/files/3406296/42899_202570y.pdf -
2Academic Journal
المؤلفون: Ferdinandusse, S., Rusch, H., van Lint, A.E.M., Dacremont, G., Wanders, R.J.A., Vreken, P.
المصدر: Journal of Lipid Research ; volume 43, issue 3, page 438-444 ; ISSN 0022-2275
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3Academic Journal
المؤلفون: de Jongh, S., Vreken, P., IJlst, L., Wanders, R.J.A., Jakobs, C.A.J.M., Bakker, H.D.
المصدر: de Jongh , S , Vreken , P , IJlst , L , Wanders , R J A , Jakobs , C A J M & Bakker , H D 1999 , ' Spontaneous pregnancy in a patient with classical galactosaemia ' , Journal of Inherited Metabolic Disease , vol. 22 , pp. 754-755 . https://doi.org/10.1023/A:1005504403173
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4Academic Journal
المؤلفون: Vreken, P., van Rooij, A., Denis, S., van Grunsven, E.G., Cuebas, D.A., Wanders, R.J.A.
المصدر: Journal of Lipid Research ; volume 39, issue 12, page 2452-2458 ; ISSN 0022-2275
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5Academic Journal
المصدر: Molecular and Cellular Biology ; volume 12, issue 7, page 2986-2996 ; ISSN 0270-7306 1098-5549
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6Academic Journal
المؤلفون: Van De Vreken, P., Gobin, A., Baken, S., Van Holm, L., Verhasselt, A., Smolders, E., Merckx, R.
المساهمون: Flemish Institute for Technological Research and Belspo
المصدر: European Journal of Soil Science ; volume 67, issue 3, page 332-340 ; ISSN 1351-0754 1365-2389
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7Academic Journal
المؤلفون: Ottoy, S., Elsen, A., Van De Vreken, P., Gobin, A., Merckx, R., Hermy, M., Van Orshoven, J.
المساهمون: Agency for Innovation by Science and Technology (IWT)
المصدر: European Journal of Soil Science ; volume 67, issue 6, page 816-826 ; ISSN 1351-0754 1365-2389
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8Book
المؤلفون: Vreken, P., van Lint, A. E. M., Bootsma, A. H., Overmars, H., Wanders, R. J. A., van Gennip, A. H.
المصدر: Current Views of Fatty Acid Oxidation and Ketogenesis ; Advances in Experimental Medicine and Biology ; page 327-337 ; ISSN 0065-2598 ; ISBN 9780306462009 9780306468186
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9
المؤلفون: Van Overtveld, K., Tits, M., Elsen, A., Van De Vreken, P., Van Orshoven, Jos, Vanderborght, Jan, Diels, Jan, Batelaan, Okke
المساهمون: Hydrology and Hydraulic Engineering, Geography
مصطلحات موضوعية: denitrification, Flanders, headwater catchment
URL الوصول: https://explore.openaire.eu/search/publication?articleId=od______3848::6dfeb83a91825be26fee1cd3703352c4
https://biblio.vub.ac.be/vubir/determination-of-denitrification-capacity-of-small-headwater-catchments-in-flanders(9b4ad9e4-4988-4206-b531-294cf9674fd9).html -
10Academic Journal
المؤلفون: Bok, L.A., Vreken, P., Wijburg, F.A., Wanders, R.J., Gregersen, N., Corydon, M.J., Waterham, H.R., Duran, M.
المصدر: Bok , L A , Vreken , P , Wijburg , F A , Wanders , R J , Gregersen , N , Corydon , M J , Waterham , H R & Duran , M 2003 , ' Short-chain Acyl-CoA dehydrogenase deficiency: studies in a large family adding to the complexity of the disorder ' , Audio-Digest Pediatrics , no. 112 , pp. 1152-1155 .
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11Academic Journal
المؤلفون: Lund, A. M., Dixon, M. A., Vreken, P., Leonard, J. V., Morris, A. A. M.
المصدر: Journal of Inherited Metabolic Disease ; volume 26, issue 4, page 410-412 ; ISSN 0141-8955 1573-2665
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12Academic Journal
المؤلفون: Assies, J., Haverkort, E. B., Lieverse, R., Vreken, P.
المصدر: Clinical Endocrinology ; volume 59, issue 4, page 459-466 ; ISSN 0300-0664 1365-2265
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13Academic Journal
المؤلفون: Lund, A. M., Dixon, M. A., Vreken, P., Leonard, J. V., Morris, A. A. M.
المصدر: Journal of Inherited Metabolic Disease ; volume 26, issue 4, page 353-360 ; ISSN 0141-8955 1573-2665
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14Academic Journal
المؤلفون: FERDINANDUSSE, S, RUSCH, H, VAN LINT, AEM, Dacremont, Georges, WANDERS, R, VREKEN, P
المصدر: JOURNAL OF LIPID RESEARCH ; ISSN: 0022-2275
مصطلحات موضوعية: Medicine and Health Sciences
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15
المؤلفون: Waterham, H. R., Koster, J., Romeijn, G. J., Vreken, P., Hennekam, R. C. M., Andersson, H. C., Fitzpatrick, D. R., Kelley, R. I., Wanders, R. J. A.
المساهمون: Paediatric Metabolic Diseases, Laboratory Genetic Metabolic Diseases, AGEM - Inborn errors of metabolism, Paediatric Genetics
المصدر: Nederlands tijdschrift voor geneeskunde, 148(5). Bohn Stafleu van Loghum
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16Academic Journal
المؤلفون: Bakker, HD, de Sonnaville, M-LCS, Vreken, P, Abeling, NGGM, Groener, JEM (Johanna), Keulemans, JLM, Diggelen, Otto
المصدر: Bakker , HD , de Sonnaville , M-LCS , Vreken , P , Abeling , NGGM , Groener , JEM , Keulemans , JLM & Diggelen , O 2001 , ' Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: no asscociation with neuroaxonal dystrophy? ' , European Journal of Human Genetics , vol. 9 , pp. 91-96 .
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17Academic Journal
المؤلفون: Moolenaar, S.H., Gohlich-Ratmann, G., Engelke, U.F.H., Spraul, M., Humpfer, E., Dvortsak, P., Voit, T., Hoffmann, G.F., Brautigam, C., Kuilenburg, A.B.P. van, Gennip, A.H. van, Vreken, P., Wevers, R.A.
المصدر: Magnetic Resonance in Medicine, 46, 5, pp. 1014-7
مصطلحات موضوعية: Neuromuscular and neurometabolic disorders, Neuromusculaire en neurometabole aandoeningen
Relation: http://hdl.handle.net/2066/185838
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18Academic Journal
المؤلفون: Tóth, G, Morava, Eva, Bene, J, Selhorst, J J, Overmars, H, Vreken, P, Molnár, J, Farkas, V, Melegh, B
مصطلحات موضوعية: Carnitine, Cerebellar Ataxia, Child, DNA, Mitochondrial, Humans, Intellectual Disability, Leigh Disease, Male, Muscular Diseases, Mutation
Relation: Journal of Inherited Metabolic Disease vol:24 issue:3 pages:421-2; https://lirias.kuleuven.be/handle/123456789/570850
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19Academic Journal
المؤلفون: Waterham, H.R., Koster, J., Romeijn, G.J., Hennekam, R.C.M., Vreken, P., Andersson, H.C., Fitzpatrick, D.R., Kelley, R.I., Wanders, R.J.A.
المصدر: Waterham , H R , Koster , J , Romeijn , G J , Hennekam , R C M , Vreken , P , Andersson , H C , Fitzpatrick , D R , Kelley , R I & Wanders , R J A 2001 , ' Mutations in the 3 beta-hydroxysterol Delta(24)-reductase gene cause desmosterolosis, an autosomal recessive disorder of ' , American Journal of Human Genetics , vol. 69 , pp. 685-694 . https://doi.org/10.1086/323473
وصف الملف: application/pdf
Relation: https://dare.uva.nl/personal/pure/en/publications/mutations-in-the-3-betahydroxysterol-delta24reductase-gene-cause-desmosterolosis-an-autosomal-recessive-disorder-of(1fce4e10-e759-4e65-aa2e-381c8d26d32c).html
الاتاحة: https://dare.uva.nl/personal/pure/en/publications/mutations-in-the-3-betahydroxysterol-delta24reductase-gene-cause-desmosterolosis-an-autosomal-recessive-disorder-of(1fce4e10-e759-4e65-aa2e-381c8d26d32c).html
https://doi.org/10.1086/323473
https://pure.uva.nl/ws/files/3274243/14423_91204y.pdf -
20Academic Journal
المؤلفون: Tóth, G., Morava, É., Bene, J., Selhorst, J. J. M., Overmars, H., Vreken, P., Molnár, J., Farkas, V., Melegh, B.
المصدر: Journal of Inherited Metabolic Disease ; volume 24, issue 3, page 421-422 ; ISSN 0141-8955 1573-2665