MuddSHLevyHLIkovbyF.Disorders in transsulfuration. In: ScriverCRBeaudetALSlyWSValleD, eds. The Metabolic and Molecular Bases of Inherited Disease.New York: McGraw-Hill, 1995: 1279–328.
2.
BoersGHJSmalsAGHTrijbelsFJMFowlerBBakkerenJAJMSchoonderwaldtHCHeterozygosity for homocystinuria in premature peripheral and cerebral occlusive arterial disease. N Engl J Med1985; 313: 709–15.
3.
GrahamIMDalyLERefsumHMRobinsonKBrattströmLEUelandPMPlasma homocysteine as a risk factor for vascular disease. The European concerted action project. JAMA1997; 277: 1775–81.
4.
FrosstPBlomHJMilosRGoyettePSheppardCAMatthewsRGA candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nat Genet1995; 10: 111–3.
5.
TsaiMY. Laboratory assessment of mild hyperhomocysteinemia as an independent risk factor for occlusive vascular diseases. Clin Chem1996; 42: 492–3.
6.
ChadefauxBRethoréMORaoulOCeballosIPoissonnierMGilgenkranzSCystathionine beta synthase: Gene dosage effect in trisomy 21. Biochem Biophys Res Comm1985; 128: 40–4.
7.
NakaiHWatkinsPCByersMGShowsTBTadaK.Site specific mapping of chromosome 21 gene probes and the study of Down syndrome. Acta Paediatr Jpn1987; 29: 510–2.
8.
DomagalaTBLiburaMSzczeklik. Hyperhomocysteinemia following oral methionine load is associated with increased lipid peroxidation. Thromb Res1997; 87: 411–6.
9.
ScheurlenM.Morbus Meulengracht [in German]. Deutsche Medizinische Wochenschrift1989; 114: 1767.
10.
SassJOEndresW.Quantitation of total homocysteine in human plasma by derivatization to its N(O,S)-propoxycarbonyl propyl ester and gas chromatography-mass spectrometry analysis. J Chromatogr A1997; 776: 342–7.
11.
Spinco Division of Beckman Instruments, Inc.The System 6300 High Performance Amino Acid Analyzer: Instruction Manual.Palo Alto: Beckman, Inc, 1982.
12.
JentzschAMBachmannHFürstPBiesalskiHK. Improved analysis of malondialdehyde in human body fluids. Free Radic Biol Med1996; 20: 251–6.
13.
LejeuneJRethoréM-Ode BloisM-CPeetersMNaffahJMegarbaneAAmino acids and Trisomy 21 [in French]. Ann Genét1992; 35: 8–13.
14.
ChadefauxBCeballosIHametMCoudeMPoissonnierMKamounPIs absence of atheroma in Down syndrome due to decreased homocysteine levels?Lancet1988; i: 741.
15.
BrattströmLIsraelssonBTengbornLHultbergB.Homocysteine, factor VII and antithrombin III in subjects with different gene dosage for cystathionine β-synthase. J Inher Metab Dis1989; 12: 475–82.
16.
HultbergBAnderssonASternerG.Plasma homocysteine in renal failure. Clin Nephrol1993; 40: 230–4.
17.
UelandPMRefsumHStablerSPMalinowRAnderssonAAllenRH. Total homocysteine in plasma or serum: Methods and clinical applications. Clin Chem1993; 39: 1764–79.
18.
NehlerMRTaylorLMPorterJM. Homocysteincmia as a risk factor for atherosclerosis: A review. Cardiovasc Pathol1997; 6: 1–9.
19.
VerhoefPKokFJKluijtmansLAJBlomHJRefsumHUelandPMThe 677C→T mutation in the methylenetetrahydrofolate reductase gene: Associations with plasma total homocysteine levels and risk of coronary atherosclerotic disease. Atherosclerosis1997; 132: 105–13.