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Full TextIssue DateTitleAuthor(s)
2011Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiencyBanka, S.; Blom, H.J.; Walter, J.; Aziz, M.; Urquhart, J.; Clouthier, C.M.; Rice, G.I.; Brouwer, A.P.M. de; Hilton, E.; Vassallo, G.; Will, A.; Smith, D.E.; Smulders, Y.M.; Wevers, R.A.; Steinfeld, R.; Heales, S.; Crow, Y.J.; Pelletier, J.N.; Jones, S.; Newman, W.G.
2011No effect of folic acid supplementation on global DNA methylation in men and women with moderately elevated homocysteineJung, A.Y.; Smulders, Y.; Verhoef, P.; Kok, F.J.; Blom, H.J.; Kok, R.M.; Kampman, E.; Durga, J.
2010Inhibition of methylation decreases osteoblast differentiation via a non-DNA-dependent methylation mechanismVaes, B.L.T.; Lute, C.; Woning, S.P. van der; Piek, E.; Vermeer, J.; Blom, H.J.; Mathers, J.C.; Muller, M.; Groot, L. de; Steegenga, W.T.
2010Maternal homocysteine and related B vitamins as risk factors for low birthweight.Hogeveen, M.; Blom, H.J.; Heijden, E.H.M. van der; Semmekrot, B.A.; Sporken, J.M.J.; Ueland, P.M.; Heijer, M. den
2010The effect of folinic acid supplementation on homocysteine concentrations in newborns.Hogeveen, M.; Heijer, M. den; Schonbeck, Y.; IJland, M.M.; Oppenraaij, D. van; Klein Gunnewiek, J.M.T.; Blom, H.J.
2010Ovarian cyst fluid of serous ovarian tumors contains large quantities of the brain amino acid N-acetylaspartate.Kolwijck, E.; Wevers, R.A.; Engelke, U.F.H.; Woudenberg, J.; Bulten, J.; Blom, H.J.; Massuger, L.F.A.G.
2010Protective effect of periconceptional folic acid supplements on the risk of congenital heart defects: a registry-based case-control study in the northern Netherlands.Beijnum, I.M. van; Kapusta, L.; Bakker, M.K.; Heijer, M. den; Blom, H.J.; Walle, H.E. de
2009High-resolution H-1 NMR spectroscopic investigation of a chick embryo model of neural tube development.Coen, M.; Wevers, R.A.; Lindon, J.C.; Blom, H.J.
2009Sedoheptulokinase deficiency due to a 57-KB deletion in cystinosis patients causes accumulation of sedoheptulose: elucidation of the function of the carkl geneWamelink, M.M.; Struys, E.A.; Jansen, E.E.W.; Zijlstra, F.S.M.; Engelke, U.F.H.; Blom, H.J.; Wevers, R.A.; Jakobs, C.; Levtchenko, E.N.
2009S-adenosylmethionine and S-adenosylhomocysteine levels in the aging brain of APP/PS1 Alzheimer mice.Hooijmans, C.R.; Blom, H.J.; Oppenraaij-Emmerzaal, D. van; Ritskes-Hoitinga, M.; Kiliaan, A.J.
2009An association study of 45 folate-related genes in spina bifida: Involvement of cubilin (CUBN) and tRNA aspartic acid methyltransferase 1 (TRDMT1).Franke, B.; Vermeulen, S.; Steegers-Theunissen, R.P.M.; Coenen, M.J.H.; Schijvenaars, M.M.V.A.P.; Scheffer, H.; Heijer, M. den; Blom, H.J.
2009N-acetyl resonances in in vivo and in vitro NMR spectroscopy of cystic ovarian tumors.Kolwijck, E.; Engelke, U.F.H.; Graaf, M. van der; Heerschap, A.; Blom, H.J.; Hadfoune, M.; Buurman, W.A.; Massuger, L.F.A.G.; Wevers, R.A.
2008Polymorphisms in catechol-O-methyltransferase and methylenetetrahydrofolate reductase in relation to the risk of schizophrenia.Muntjewerff, J.W.; Gellekink, H.; Heijer, M. den; Hoogendoorn, M.L.; Kahn, R.S.; Sinke, R.J.; Blom, H.J.
2008Sedoheptulokinase deficiency due to a 57-kb deletion in cystinosis patients causes urinary accumulation of sedoheptulose: elucidation of the CARKL gene.Wamelink, M.M.; Struys, E.A.; Jansen, E.E.; Levtchenko, E.N.; Zijlstra, F.S.; Engelke, U.; Blom, H.J.; Jakobs, C.; Wevers, R.A.
2008Role for mitochondrial uncoupling protein-2 (UCP2) in hyperhomocysteinemia and venous thrombosis risk?Heill, S.G.; Vermeulen, H.H.M.; Rijt-Pisa, B.J.M. van der; Heijer, M. den; Blom, H.J.
2008Common 894G>T single nucleotide polymorphism in the gene coding for endothelial nitric oxide synthase (eNOS) and risk of congenital heart defects.Beynum, I.M. van; Mooij, C.; Kapusta, L.; Heil, S.; Heijer, M. den; Blom, H.J.
2008Inhibition of methylation and changes in gene expression in relation to neural tube defects.Linden, I.J. van der; Heil, S.G.; Petersen, M.; Straaten, H.W.M. van; Heijer, M. den; Blom, H.J.
2007Response: Homocysteine lowering and recurrent venous thrombosis: the VITRO trial [Letter].Heijer, M. den; Heijer, M. den; Blom, H.J.; Rosendaal, F.R.; Bos, G.M.
2007Diet-induced hyperhomocysteinemia does not lead to large gene-expression differences in rat aorta.Heil, S.G.; Kluijtmans, L.A.J.; Vriese, A.S. de; Pfundt, R.; Blom, H.J.
2007The methylenetetrahydrofolate dehydrogenase (MTHFD1) 1958G>A variant is not associated with spina bifida risk in the Dutch population.Linden, I.J. van der; Heil, S.G.; Kouwenberg, I.C.; Heijer, M. den; Blom, H.J.
2007No evidence for a preferential transmission of the methylenetetrahydrofolate reductase 677T allele in families with schizophrenia offspringMuntjewerff, J.W.; Hoogendoorn, M.L.; Aukes, M.F.; Kahn, R.S.; Sinke, R.J.; Blom, H.J.; Heijer, M. den
2007Molecular genetic analysis of the human dihydrofolate reductase gene: relation with plasma total homocysteine, serum and red blood cell folate levels.Gellekink, H.; Blom, H.J.; Linden, I.J. van der; Heijer, M. den; Heijer, M. den
2007DNA methylation status is not impaired in treated cystathionine beta-synthase (CBS) deficient patients.Heil, S.G.; Riksen, N.P.; Boers, G.H.J.; Smulders, Y.; Blom, H.J.
2007A simple high-throughput method for the determination of plasma methylmalonic acid by liquid chromatography-tandem mass spectrometry.Blom, H.J.; Rooij, A. van; Hogeveen, M.
2007The 894G>T variant in the endothelial nitric oxide synthase gene and spina bifida riskLinden, I.J. van der; Heil, S.G.; Heijer, M. den; Heijer, M. den; Blom, H.J.
2007Homocysteine lowering by B vitamins and the secondary prevention of deep vein thrombosis and pulmonary embolism: A randomized, placebo-controlled, double-blind trial.Heijer, M. den; Willems, H.P.J.; Blom, H.J.; Gerrits, W.B.J.; Cattaneo, M.; Eichinger, S.; Rosendaal, F.R.; Bos, G.M.
2007The effect of homocysteine reduction by B-vitamin supplementation on inflammatory markers.Peeters, A.C.T.; Aken, B.E. van; Blom, H.J.; Reitsma, P.H.; Heijer, M. den; Heijer, M. den
2007Cystine dimethylester model of cystinosis: still reliable?Wilmer, M.J.G.; Willems, P.H.G.M.; Verkaart, S.A.J.; Visch, H.J.; Graaf-Hess, A.C. de; Blom, H.J.; Monnens, L.A.H.; Heuvel, L.P.W.J. van den; Levtchenko, E.N.
2007No interaction between factor V Leiden and hyperhomocysteinemia or MTHFR 677TT genotype in venous thrombosis. Results of a meta-analysis of published studies and a large case-only study.Keijzer, M.B.; Borm, G.F.; Blom, H.J.; Bos, G.M.; Rosendaal, F.R.; Heijer, M. den; Heijer, M. den
2007The MTHFR 677C->T polymorphism and the risk of congenital heart defects : a literature review and meta-analysisBeijnum, I.M. van; Heijer, M. den; Heijer, M. den; Blom, H.J.; Kapusta, L.
2007The association of betaine, homocysteine and related metabolites with cognitive function in Dutch elderly people.Eussen, S.; Ueland, P.M.; Clarke, R.; Blom, H.J.; Hoefnagels, W.H.L.; Staveren, W.A. van; Groot, L.C. de
2007Variation and expression of dihydrofolate reductase (DHFR) in relation to spina bifida.Linden, I.J. van der; Nguyen, U.; Heil, S.G.; Franke, B.; Vloet, S.T.M.; Gellekink, H.; Heijer, M. den; Blom, H.J.
2007Associations of common polymorphisms in the thymidylate synthase, reduced folate carrier and 5-aminoimidazole-4-carboxamide ribonucleotide transformylase/inosine monophosphate cyclohydrolase genes with folate and homocysteine levels and venous thrombosis risk.Gellekink, H.; Blom, H.J.; Heijer, M. den; Heijer, M. den
2007Marfanoid features in a child with combined methylmalonic aciduria and homocystinuria (CblC type).Heil, S.G.; Hogeveen, M.; Kluijtmans, L.A.J.; Dijken, P.J. van; Berg, G.B. van de; Blom, H.J.; Morava, E.
2007The origin of halitosis in cystinotic patients due to cysteamine treatment.Besouw, M.; Blom, H.J.; Tangerman, A.; Graaf-Hess, A.C. de; Levtchenko, E.N.
2007Low vitamin B6, and not plasma homocysteine concentration, as risk factor for abdominal aortic aneurysm: a retrospective case-control study.Peeters, A.C.T.; Landeghem, B.A.J. van; Graafsma, S.J.; Kranendonk, S.E.; Hermus, A.R.M.M.; Blom, H.J.; Heijer, M. den; Heijer, M. den
2007Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk.Gellekink, H.; Muntjewerff, J.W.; Vermeulen, S.; Hermus, A.R.M.M.; Blom, H.J.; Heijer, M. den; Heijer, M. den
2007Diversity of cystathionine beta-synthase haplotypes bearing the most common homocystinuria mutation c.833T>C: a possible role for gene conversion.Vyletal, P.; Sokolova, J.; Cooper, D.N.; Kraus, J.P.; Krawczak, M.; Pepe, G.; Rickards, O.; Koch, H.G.; Linnebank, M.; Kluijtmans, L.A.J.; Blom, H.J.; Boers, G.H.J.; Gaustadnes, M.; Skovby, F.; Wilcken, B.; Wilcken, D.E.L.; Andria, G.; Sebastio, G.; Naughten, E.R.; Yap, S.; Ohura, T.; Pronicka, E.; Laszlo, A.; Kozich, V.
2006Can we exclude the TXNIP gene as a candidate gene for familial combined hyperlipidemia?Vleuten, G.M. van der; Hijmans, A.G.M.; Heil, S.G.; Blom, H.J.; Stalenhoef, A.F.H.; Graaf, J. de
2006Neural tube defects and folate: case far from closed.Blom, H.J.; Shaw, G.M.; Heijer, M. den; Finnell, R.H.
2006Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: an overview.Castro, R.; Rivera, I.; Blom, H.J.; Jakobs, C.; Almeida, I.T. de
2006No effect of folic acid and methionine supplementation on D4Z4 methylation in patients with facioscapulohumeral muscular dystrophy.Kooi, E.L. van der; Greef, J.C. de; Wohlgemuth, M.; Frants, R.R.; Asseldonk, R.J. van; Blom, H.J.; Engelen, B.G.M. van; Maarel, S.M. van der; Padberg, G.W.A.M.
2006Genetic variation in genes of folate metabolism and neural-tube defect risk.Linden, I.J. van der; Afman, L.A.; Heil, S.G.; Blom, H.J.
2006Association of a 31 bp VNTR in the CBS gene with postload homocysteine concentrations in the Framingham Offspring Study.Lievers, K.J.; Kluijtmans, L.A.J.; Blom, H.J.; Wilson, P.W.; Selhub, J.; Ordovas, J.M.
2006The Gln223Arg polymorphism in the leptin receptor is associated with familial combined hyperlipidemia.Vleuten, G.M. van der; Kluijtmans, L.A.J.; Hijmans, A.G.M.; Blom, H.J.; Stalenhoef, A.F.H.; Graaf, J. de
2006Migraine and MTHFR C677T genotype in a population-based sample.Scher, A.I.; Terwindt, G.M.; Verschuren, W.M.M.; Kruit, M.C.; Blom, H.J.; Kowa, H.; Frants, R.R.; Maagdenberg, A.M.J.M. van den; Buchem, M.A. van; Ferrari, M.; Launer, L.J.
2006Homocysteine, methylenetetrahydrofolate reductase and risk of schizophrenia: a meta-analysis.Muntjewerff, J.W.; Kahn, R.S.; Blom, H.J.; Heijer, M. den
2006Homocysteine and cognitive function in institutionalised elderly A cross-sectional analysis.Manders, M.; Vasse, E.; Groot, L.C. de; Staveren, W.A. van; Bindels, J.G.; Blom, H.J.; Hoefnagels, W.H.L.
2006No added value of the methionine loading task in assessment for venous thrombosis and cardiovascular disease risk.Keijzer, M.B.; Verhoef, P.; Borm, G.F.; Blom, H.J.; Heijer, M. den
2006Low fasting methionine concentration as a novel risk factor for recurrent venous thrombosis.Keijzer, M.B.; Heijer, M. den; Borm, G.F.; Blom, H.J.; Vollset, S.E.; Hermus, A.R.M.M.; Ueland, P.M.

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