Hyperhomocysteinemia in terms of steady-state kinetics H. RefsumA. B. GuttormsenP. M. Ueland Pages: S45 - S49
Methylenetetrahydrofolate reductase and methionine synthase: biochemistry and molecular biology R. G. MatthewsC. SheppardC. Goulding Pages: S54 - S59
Clinical aspects of cystathionine β-synthase deficiency: how wide is the spectrum? R. De FranchisM. P. SperandeoThe Italian Collaborative Study Group on Homocystinuria Pages: S67 - S70
Homocysteic and homocysteine sulphinic acid exhibit excitotoxicity in organotypic cultures from rat brain B. Flott-RahmelM. SchürmannK. Ullrich Pages: S112 - S117
Abnormalities of vascular function in hyperhomocysteinaemia: relationship to atherothrombotic disease C. D. A. StehouwerC. Jakobs Pages: S107 - S111
Relevance of vitamins, homocysteine and other metabolites in neuropsychiatric disorders R. H. AllenS. P. StablerJ. Lindenbaum Pages: S122 - S126
Mutated 5,10-methylenetetrahydrofolate reductase and moderate hyperhomocysteinaemia H. J. Blom Pages: S131 - S134
Biochemistry and molecular genetics of cystathionine β-synthase deficiency J. P. Kraus Pages: S50 - S53
Newborn screening for homocystinuria: Irish and world experience E. R. NaughtenS. YapP. D. Mayne Pages: S84 - S87
Strategies for the treatment of cystathionine β-synthase deficiency: the experience of the Willink Biochemical Genetics Unit over the past 30 years J. H. WalterJ. E. WraithJ. Till Pages: S71 - S76
Moderate hyperhomocysteinaemia and vascular disease: evidence, relevance and the effect of treatment G. H. J. Boers Pages: S127 - S130
The redox status of aminothiols as a clue to homocysteine-induced vascular damage? H. G. KochM. GoebelerE. Harms Pages: S102 - S106
Vitamins B12, B6 and folate as determinants of homocysteine concentration in the healthy population K. PietrzikA. Brönstrup Pages: S135 - S138
Remethylation defects: guidelines for clinical diagnosis and treatment H. Ogier de BaulnyM. GérardJ. Zittoun Pages: S77 - S83
Ocular complications and a new surgical approach to lens dislocation in homocystinuria due to cystathionine-β-synthetase deficiency H. Gerding Pages: S94 - S101