Homocystinuria : what about mild hyperhomocysteinaemia ?VAN DEN BERG, M; BOERS, G. H. J.Postgraduate medical journal. 1996, Vol 72, Num 851, pp 513-518, issn 0032-5473Article

Hyperhomocysteinaemia : a newly recognized risk factor for vascular diseaseBOERS, G. H. J.Netherlands journal of medicine. 1994, Vol 45, Num 1, pp 34-41, issn 0300-2977Conference Paper

Hyperhomocysteinemia as a risk factor for arterial and venous disease. A review of evidence and relevanceBOERS, G. H. J.Thrombosis and haemostasis. 1997, Vol 78, Num 1, pp 520-522, issn 0340-6245Conference Paper

The case for mild hyperhomocysteinaemia as a risk factorBOERS, G. H. J.Journal of inherited metabolic disease. 1997, Vol 20, Num 2, pp 301-306, issn 0141-8955Conference Paper

Homocysteine metabolism in endothelial cells of a patient homozygous for cystathionine β-synthase (CS) deficiencyVAN DER MOLEN, E. F; HIIPAKKA, M. J; VAN LITH-ZANDERS, H et al.Thrombosis and haemostasis. 1997, Vol 78, Num 2, pp 827-833, issn 0340-6245Conference Paper

Delay in diagnosis of homocystinuria : retrospective study of consecutive patientsCRUYSBERG, J. R. M; BOERS, G. H. J; TRIJBELS, J. M. F et al.BMJ. British medical journal (International ed.). 1996, Vol 313, Num 7064, pp 1037-1040, issn 0959-8146Article

Hyperhomocysteinemia in premature arterial disease : examination of cystathionine β-synthase alleles at the molecular levelKOZICH, V; KRAUS, E; DE FRANCHIS, R et al.Human molecular genetics (Print). 1995, Vol 4, Num 4, pp 623-629, issn 0964-6906Article

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemiaENGBERSEN, A. M. T; FRANKEN, D. G; BOERS, G. H. J et al.American journal of human genetics. 1995, Vol 56, Num 1, pp 142-150, issn 0002-9297Article

Maternal hyperhomocysteinemia : a risk factor for neural-tube defects ?STEEGERS-THEUNISSEN, R. P. M; BOERS, G. H. J; TRIJBELS, F. J. M et al.Metabolism, clinical and experimental. 1994, Vol 43, Num 12, pp 1475-1480, issn 0026-0495Article

Transamination of methionine in humansBLOM, H. J; BOERS, G. H. J; VAN DEN ELZEN, J. P. A. M et al.Clinical science (1979). 1989, Vol 76, Num 1, pp 43-49, issn 0143-5221Article

A clinical and cardiovascular survey of Ehlers-Danlos syndrome patients with complete deficiency of tenascin-XPEETERS, A. C. T. M; KUCHAREKOVA, M; TIMMERMANS, J et al.Netherlands journal of medicine. 2004, Vol 62, Num 5, pp 160-162, issn 0300-2977, 3 p.Article

Homozygous cystathionine β-synthase deficiency, combined with factor V Leiden or thermolabile methylenetetrahydrofolate reductase in the risk of venous thrombosisKLUIJTMANS, L. A. J; BOERS, G. H. J; VERBRUGGEN, B et al.Blood. 1998, Vol 91, Num 6, pp 2015-2018, issn 0006-4971Article

Plasma homocysteine and menopausal statusWOUTERS, M. G. A. J; MOORREES, M. T. E. C; VAN DER MOOREN, M. J et al.European journal of clinical investigation. 1995, Vol 25, Num 11, pp 801-805, issn 0014-2972Conference Paper

Combined vitamin B₆ plus folic acid therapy in young patients with arteriosclerosis and hyperhomocysteinemiaVAN DEN BERG, M; FRANKEN, D. G; BOERS, G. H. J et al.Journal of vascular surgery. 1994, Vol 20, Num 6, pp 933-940, issn 0741-5214Article

Hyperhomocysteinemia in retinal artery and retinal vein occlusionWENZLER, E. M; RADEMAKERS, A. J. J. M; BOERS, G. H. J et al.American journal of ophthalmology. 1993, Vol 115, Num 2, pp 162-167, issn 0002-9394Article

Lipid peroxidation in homocysteinaemiaBLOM, H. J; ENGELEN, D. P. E; BOERS, G. H. J et al.Journal of inherited metabolic disease. 1992, Vol 15, Num 3, pp 419-422, issn 0141-8955Conference Paper

Alternative methionine degradation via the transamination pathway : an option for therapy for homocystinuria due to cystathionine synthase deficiencyBLOM, H. J; BOERS, G. H. J; TANGERMAN, A et al.Journal of inherited metabolic disease. 1991, Vol 14, Num 3, pp 375-378, issn 0141-8955Article

Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblastsBOERS, G. H. J; FOWLER, B; SMALS, A. G. H et al.Human genetics. 1985, Vol 69, Num 2, pp 164-169, issn 0340-6717Article

Differential effect of single high dose and divided small dose administration of human chorionic gonadotropin on Leydig cell steroidogenic desensitizationSMALS, A. G. H; PIETERS, G. F. F. M; BOERS, G. H. J et al.The Journal of clinical endocrinology and metabolism. 1984, Vol 58, Num 2, pp 327-331, issn 0021-972XArticle

Homocysteine, vitamin status and risk of vascular disease : Effects of gender and menopausal statusVERHOEF, P; MELEADY, R; DALY, L. E et al.European heart journal. 1999, Vol 20, Num 17, pp 1234-1244, issn 0195-668XArticle

The molecular basis of cystathionine β-Synthase deficiency in Dutch patients with homocystinuria : Effect of CBS genotype on biochemical and clinical phenotype and on response to treatmentKLUIJTMANS, L. A. J; BOERS, G. H. J; KRAUS, J. P et al.American journal of human genetics. 1999, Vol 65, Num 1, pp 59-67, issn 0002-9297Article

Methylenetetrahydrofolate reductase polymorphism affects the change in homocysteine and folate concentrations resulting from low dose folic acid supplementation in women with unexplained recurrent miscarriagesNELEN, W. L. D. M; BLOM, H. J; THOMAS, C. M. G et al.The Journal of nutrition. 1998, Vol 128, Num 8, pp 1336-1341, issn 0022-3166Article

Optic neuropathy in McCune-Albright syndrome : An indication for aggressive treatmentBOCCA, G; DE VRIES, J; CRUYSBERG, J. R. M et al.Acta paediatrica (Oslo). 1998, Vol 87, Num 5, pp 599-600, issn 0803-5253Article

Carotid and femoral artery wall thickness and stiffness in patients at risk for cardiovascular disease, with special emphasis on hyperhomocysteinemiaSMILDE, T. J; VAN DEN BERKMORTEL, F. W. P. J; BOERS, G. H. J et al.Arteriosclerosis, thrombosis, and vascular biology. 1998, Vol 18, Num 12, pp 1958-1963, issn 1079-5642Article

Plasma homocysteine as a risk factor for vascular disease: The European concerted action projectGRAHAM, I. M; DALY, L. E; UITERWAAL, C. S et al.JAMA, the journal of the American Medical Association. 1997, Vol 277, Num 22, pp 1775-1781, issn 0098-7484Article