Hyperhomocysteinemia as a Risk Factor for Deep-Vein Thrombosis von den Heijer, Martin, Koster, Ted, Blom, Henk J, Bos, Gerard M.J, Briët, Ernest, Reitsma, Pieter H, Vandenbroucke, Jan P, Rosendaal, Frits R

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Betaine and Folate Status as Cooperative Determinants of Plasma Homocysteine in Humans von Holm, Pål I, Ueland, Per M, Vollset, Stein Emil, Midttun, Øivind, Blom, Henk J, Keijzer, Miranda B.A.J, den Heijer, Martin

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Enhanced Cellular Adenosine Uptake Limits Adenosine Receptor Stimulation in Patients With Hyperhomocysteinemia von Riksen, Niels P, Rongen, Gerard A, Boers, Godfried H.J, Blom, Henk J, van den Broek, Petra H.H, Smits, Paul

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Combination of CSF N-acetylaspartate and neurofilaments in multiple sclerosis von TEUNISSEN, C. E, IACOBAEUS, E, JAKOBS, C, DIJKSTRA, C. D, KHADEMI, M, BRUNDIN, L, NORGREN, N, KOEL-SIMMELINK, M. J. A, SCHEPENS, M, BOUWMAN, F, TWAALFHOVEN, H. A. M, BLOM, H. J

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Adenosine Kinase Deficiency Disrupts the Methionine Cycle and Causes Hypermethioninemia, Encephalopathy, and Abnormal Liver Function von Bjursell, Magnus K., Blom, Henk J., Cayuela, Jordi Asin, Engvall, Martin L., Lesko, Nicole, Balasubramaniam, Shanti, Brandberg, Göran, Halldin, Maria, Falkenberg, Maria, Jakobs, Cornelis, Smith, Desiree, Struys, Eduard, von Döbeln, Ulrika, Gustafsson, Claes M., Lundeberg, Joakim, Wedell, Anna

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Homocysteine metabolism, hyperhomocysteinaemia and vascular disease: An overview von Castro, R., Rivera, I., Blom, H. J., Jakobs, C., Almeida, I. Tavares

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Choline and Risk of Neural Tube Defects in a Folate-fortified Population von Shaw, Gary M., Finnell, Richard H., Blom, Henk J., Carmichael, Suzan L., Vollset, Stein Emil, Yang, Wei, Ueland, Per M.

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Consensus recommendations for the diagnosis, treatment and follow-up of inherited methylation disorders von Barić, Ivo, Staufner, Christian, Augoustides-Savvopoulou, Persephone, Chien, Yin-Hsiu, Dobbelaere, Dries, Grünert, Sarah C., Opladen, Thomas, Petković Ramadža, Danijela, Rakić, Bojana, Wedell, Anna, Blom, Henk J.

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5,10-methylenetetrahydrofolate reductase (MTHFR) 677C→T and 1298A→C mutations are associated with DNA hypomethylation von Castro, R, Rivera, I, Ravasco, P, Camilo, M E, Jakobs, C, Blom, H J, de Almeida, I T

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MTHFR 677C→T Polymorphism and Risk of Coronary Heart Disease: A Meta-analysis von Klerk, Mariska, Verhoef, Petra, Clarke, Robert, Blom, Henk J, Kok, Frans J, Schouten, Evert G, and the MTHFR Studies Collaboration Group

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Cysteamine revisited: repair of arginine to cysteine mutations von Gallego-Villar, L., Hannibal, Luciana, Häberle, J., Thöny, B., Ben-Omran, T., Nasrallah, G. K., Dewik, Al-N., Kruger, W. D., Blom, H. J.

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Increased Homocysteine and S-Adenosylhomocysteine Concentrations and DNA Hypomethylation in Vascular Disease von Castro, Rita, Rivera, Isabel, Struys, Eduard A, Jansen, Erwin E.W, Ravasco, Paula, Camilo, Maria Ermelinda, Blom, Henk J, Jakobs, Cornelis, Tavares de Almeida, Isabel

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A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects? von van der Put, Nathalie M.J., Gabreëls, Fons, Stevens, Erik M.B., Smeitink, Jan A.M., Trijbels, Frans J.M., Eskes, Tom K.A.B., van den Heuvel, Lambert P., Blom, Henk J.

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Migraine and MTHFR C677T genotype in a population-based sample von Scher, Ann I., Terwindt, Gisela M., Verschuren, W. M. Monique, Kruit, Mark C., Blom, Henk J., Kowa, Hisanori, Frants, Rune R., van den Maagdenberg, Arn M. J. M., van Buchem, Mark, Ferrari, Michel D., Launer, Lenore J.

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The MTHFR 677C→T polymorphism and the risk of congenital heart defects: a literature review and meta-analysis von van Beynum, I.M., den Heijer, M., Blom, H.J., Kapusta, L.

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Hyperhomocysteinemia, MTHFR, and risk of vascular disease von Blom, H J, Verhoef, D P

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Maternal MTHFR 677C>T is a risk factor for congenital heart defects: effect modification by periconceptional folate supplementation von van Beynum, Ingrid M., Kapusta, Livia, den Heijer, Martin, Vermeulen, Sita H.H.M., Kouwenberg, Margreet, Daniëls, Otto, Blom, Henk J.

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Hyperhomocysteinemia and recurrent early pregnancy loss: a meta-analysis von Nelen, Willianne L.D.M, Blom, Henk J, Steegers, Eric A.P, den Heijer, Martin, Eskes, Tom K.A.B

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A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase von Frosst, P, Blom, H.J, Milos, R, Goyette, P, Sheppard, C.A, Matthews, R.G, Boers, G.J.H, den Heijer, M, Kluijtmans, L.A.J, van den Heuve, L.P, Rozen, R

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Folate, Homocysteine and Neural Tube Defects: An Overview von Van Der Put, Nathalie M.J., Van Straaten, Henny W.M., Trijbels, Frans J.M., Blom, Henk J.

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