Defective glucuronic acid transport from lysosomes of infantile free sialic acid storage disease fibroblasts.

Por Blom, H J, Andersson, H C, Seppala, R, Tietze, F, Gahl, W A
Publicado em 1990

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

Protection against lethal Sendai virus infection by in vivo priming of virus-specific cytotoxic T lymphocytes with a free synthetic peptide.

Por Kast, W M, Roux, L, Curren, J, Blom, H J, Voordouw, A C, Meloen, R H, Kolakofsky, D, Melief, C J
Publicado em 1991

Transsulfuration in an adult with hepatic methionine adenosyltransferase deficiency.

Por Gahl, W A, Bernardini, I, Finkelstein, J D, Tangerman, A, Martin, J J, Blom, H J, Mullen, K D, Mudd, S H
Publicado em 1988

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

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

Por van der Put, N M, Gabreëls, F, Stevens, E M, Smeitink, J A, Trijbels, F J, Eskes, T K, van den Heuvel, L P, Blom, H J
Publicado em 1998

Cellular hypomethylation is associated with impaired nitric oxide production by cultured human endothelial cells

Por Barroso, M., Rocha, M. S., Esse, R., Gonçalves, I., Gomes, A. Q., Teerlink, T., Jakobs, C., Blom, H. J., Loscalzo, J., Rivera, I., de Almeida, I. Tavares, Castro, R.
Publicado em 2011

Decrease in S-adenosylmethionine synthesis by 6-mercaptopurine and methylmercaptopurine ribonucleoside in Molt F4 human malignant lymphoblasts.

Por Stet, E H, De Abreu, R A, Bökkerink, J P, Blom, H J, Lambooy, L H, Vogels-Mentink, T M, de Graaf-Hess, A C, van Raay-Selten, B, Trijbels, F J
Publicado em 1994

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