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 and folate status in methotrexate-treated patients with rheumatoid arthritisVAN EDE, A. E; LAAN, R. F. J. M; BLOM, H. J et al.Rheumatology (Oxford. Print). 2002, Vol 41, Num 6, pp 658-665, issn 1462-0324Article

Hyperhomocysteinaemia : a role in the accelerated atherogenesis of chronic renal failure ?JANSSEN, M. J. F. M; VAN DEN BERG, M; STEHOUWER, C. D. A et al.Netherlands journal of medicine. 1995, Vol 46, Num 5, pp 244-251, issn 0300-2977Conference Paper

Effect of various regimens of vitamin B₆ and folic acid on mild hyperhomocysteinaemia in vascular patientsFRANKEN, D. G; BOERS, G. H. J; BLOM, H. J et al.Journal of inherited metabolic disease. 1994, Vol 17, Num 1, pp 159-162, issn 0141-8955Conference Paper

The natural history of homocystinura due to cystathionine β-synthase deficiencyMUDD, S. H; SKOVBY, F; FOWLER, B et al.American journal of human genetics. 1985, Vol 37, Num 1, pp 1-31, issn 0002-9297Article

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

Methionine transamination in patients with homocystinuria due to cystathionine β-synthase deficiencyTANGERMAN, A; WILCKEN, B; LEVY, H. L et al.Metabolism, clinical and experimental. 2000, Vol 49, Num 8, pp 1071-1077, issn 0026-0495Article

Thermolabile methylenetetrahydrofolate reductase in coronary artery diseaseKLUIJTMANS, L. A. J; KASTELEIN, J. J. P; VERHEUGT, F. W. A et al.Circulation (New York, N.Y.). 1997, Vol 96, Num 8, pp 2573-2577, issn 0009-7322Article

Hyperhomocysteinemia : a risk factor for placental abruption or infarctionGODDIJN-WESSEL, T. A; WOUTERS, M. G. A. J; MOLEN, E. F. V. D et al.European journal of obstetrics, gynecology, and reproductive biology. 1996, Vol 66, Num 1, pp 23-29, issn 0301-2115Article

Molecular genetic analysis in mild hyperhomocysteinemia : A common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk facotr for cardiovascular diseaseKLUIJTMANS, L. A. J; VAN DEN HEUVEL, L. P. W. J; BOERS, G. H. J et al.American journal of human genetics. 1996, Vol 58, Num 1, pp 35-41, issn 0002-9297Article

Prevalence of familial mild hyperhomocysteinemiaFRANKEN, D. G; BOERS, G. H. J; BLOM, H. J et al.Atherosclerosis. 1996, Vol 125, Num 1, pp 71-80, issn 0021-9150Article

Predictive value of luteinizing hormone releasing hormone (LHRH) bolus testing before and after 36-hour pulsatile LHRH administration in the differential diagnosis of constitutional delay of puberty and male hypogonadotropic hypogonadismSMALS, A. G. H; HERMUS, A. R. M; BOERS, G. H. J et al.The Journal of clinical endocrinology and metabolism. 1994, Vol 78, Num 3, pp 602-608, issn 0021-972XArticle

Reciprocal inhibition of the long-acting luteinizing hormone releasing hormone agonist Buserelin and human chorionic gonadotropin in stimulating Leydig cell steroidogenesisSMALS, A. G. H; PIETERS, G. F. F. M; SMALS, A. E. M et al.Journal of steroid biochemistry. 1987, Vol 28, Num 6, pp 743-747, issn 0022-4731Article

Heterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial diseaseBOERS, G. H. J; SMALS, A. G. H; TRIJBELS, F. J. M et al.The New England journal of medicine. 1985, Vol 313, Num 12, pp 709-715, issn 0028-4793Article

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