Homocystinuria: what about mild hyperhomocysteinaemia?

Por van den Berg, M., Boers, G. H.
Publicado em 1996

Delay in diagnosis of homocystinuria: retrospective study of consecutive patients.

Por Cruysberg, J. R., Boers, G. H., Trijbels, J. M., Deutman, A. F.
Publicado em 1996

Unique efficiency of methionine metabolism in premenopausal women may protect against vascular disease in the reproductive years.

Por Boers, G H, Smals, A G, Trijbels, F J, Leermakers, A I, Kloppenborg, P W
Publicado em 1983

Thermolabile 5,10-methylenetetrahydrofolate reductase as a cause of mild hyperhomocysteinemia.

Por Engbersen, A M, Franken, D G, Boers, G H, Stevens, E M, Trijbels, F J, Blom, H J
Publicado em 1995

The molecular basis of cystathionine beta-synthase deficiency in Dutch patients with homocystinuria: effect of CBS genotype on biochemical and clinical phenotype and on response to...

Por Kluijtmans, L A, Boers, G H, Kraus, J P, van den Heuvel, L P, Cruysberg, J R, Trijbels, F J, Blom, H J
Publicado em 1999

Defective cystathionine beta-synthase regulation by S-adenosylmethionine in a partially pyridoxine responsive homocystinuria patient.

Por Kluijtmans, L A, Boers, G H, Stevens, E M, Renier, W O, Kraus, J P, Trijbels, F J, van den Heuvel, L P, Blom, H J
Publicado em 1996

Molecular genetic analysis in mild hyperhomocysteinemia: a common mutation in the methylenetetrahydrofolate reductase gene is a genetic risk factor for cardiovascular disease.

Por Kluijtmans, L. A., van den Heuvel, L. P., Boers, G. H., Frosst, P., Stevens, E. M., van Oost, B. A., den Heijer, M., Trijbels, F. J., Rozen, R., Blom, H. J.
Publicado em 1996