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Prof.dr. H.J. Blom
Completed research (5)
Homocysteine; Folate; Neural tube defects; methylation; Coronary artery disease; newborn screeing, inborn errors of metabolism; inherited metabolic diseases
Homocysteine; Foliumzuur; Neuraalbuis defecten; Methylering; Hart- en vaatziekten; hielprik screening; erfelijke metabole ziekten
Digital Author ID
Department of Clinical Chemistry (VU)
Inherited metabolic diseases
Erfelijke metabole ziekten
h. blom -at- vumc. nl
(the most recent at the top)
Genome sequence of the naturally plasmid-free Lactobacillus plantarum strain NC8 (CCUG 61730).
Maternal homocysteine and small-for-gestational-age offspring: systematic review and meta-analysis.
Asymmetric dimethylarginine in adults with cystathionine beta-synthase deficiency.
A liquid chromatography mass spectrometry method for the measurement of cystathionine beta-synthase activity in cell extracts
Identification and characterization of an inborn error of metabolism caused by dihydrofolate reductase deficiency
Completed research projects
(the most recent research is at the top)
Determinants of DNA-methylation in sporadic and familial colorectal carcinogenesis: individual susceptibility and B-vitamin status.
Neural tube defects and reduced methylation of DNA
Etiology of neural tube defects that can be prevented by folic acid; teratology of homocysteine on neural tube defects
Molecular genetic basis of hyperhomocysteinemia.
Comparitive study on the utilization of folic acid and methyltetrahydrofolic acid in cardiovascular patients with thermolabile variant of N5-N10 MTHFR and patients with normal MTHFR activity.
Public health and health care
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Royal Netherlands Academy of Arts and Sciences
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