110 related articles for article (PubMed ID: 9550528)
21. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.
Kadziela J; Janas J; Dzielińska Z; Szperl M; Gaździk D; Chotkowska E; Piotrowski W; Ruzyłło W
Kardiol Pol; 2003 Jul; 59(7):17-26; discussion 26. PubMed ID: 14560345
[TBL] [Abstract][Full Text] [Related]
22. Major determinants of hyperhomocysteinemia in peritoneal dialysis patients.
Vychytil A; Födinger M; Wölfl G; Enzenberger B; Auinger M; Prischl F; Buxbaum M; Wiesholzer M; Mannhalter C; Hörl WH; Sunder-Plassmann G
Kidney Int; 1998 Jun; 53(6):1775-82. PubMed ID: 9607212
[TBL] [Abstract][Full Text] [Related]
23. Homocysteinemia is inversely correlated with platelet count and directly correlated with sE- and sP-selectin levels in females homozygous for C677T methylenetetrahydrofolate reductase.
Rongioletti M; Baldassini M; Papa F; Capoluongo E; Rocca B; Cristofaro RD; Salvati G; Larciprete G; Stroppolo A; Angelucci PA; Cirese E; Ameglio F
Platelets; 2005; 16(3-4):185-90. PubMed ID: 16011963
[TBL] [Abstract][Full Text] [Related]
24. MS-PCR assay to detect 677C-->T mutation in the 5,10-methylenetetrahydrofolate reductase gene.
Hill AE; FitzPatrick DR
J Inherit Metab Dis; 1998 Aug; 21(6):694-5. PubMed ID: 9762616
[No Abstract] [Full Text] [Related]
25. Mutated 5,10-methylenetetrahydrofolate reductase, hyperhomocysteinemia and risk for cardiovascular disease. Nature, nurture or nonsense?
Blom HJ
Eur J Clin Invest; 2001 Jan; 31(1):6-8. PubMed ID: 11168432
[No Abstract] [Full Text] [Related]
26. Genotype-independent in vivo oxidative stress following a methionine loading test: maximal platelet activation in subjects with early-onset thrombosis.
Di Minno MN; Pezzullo S; Palmieri V; Coppola A; D'Angelo A; Sampietro F; Cavalca V; Tremoli E; Di Minno G
Thromb Res; 2011 Oct; 128(4):e43-8. PubMed ID: 21669453
[TBL] [Abstract][Full Text] [Related]
27. Elevated plasma homocysteine was associated with hemorrhagic and ischemic stroke, but methylenetetrahydrofolate reductase gene C677T polymorphism was a risk factor for thrombotic stroke: a Multicenter Case-Control Study in China.
Li Z; Sun L; Zhang H; Liao Y; Wang D; Zhao B; Zhu Z; Zhao J; Ma A; Han Y; Wang Y; Shi Y; Ye J; Hui R;
Stroke; 2003 Sep; 34(9):2085-90. PubMed ID: 12907815
[TBL] [Abstract][Full Text] [Related]
28. Nutrigenetic impact of daily folate intake on plasma homocysteine and folate levels in patients with different methylenetetrahydrofolate reductase genotypes.
Messika AH; Kaluski DN; Lev E; Iakobishvili Z; Shohat M; Hasdai D; Mager A
Eur J Cardiovasc Prev Rehabil; 2010 Dec; 17(6):701-5. PubMed ID: 20421795
[TBL] [Abstract][Full Text] [Related]
29. Severe methylenetetrahydrofolate reductase deficiency, methionine synthase, and nitrous oxide--a cautionary tale.
Erbe RW; Salis RJ
N Engl J Med; 2003 Jul; 349(1):5-6. PubMed ID: 12840086
[No Abstract] [Full Text] [Related]
30. Methylenetetrahydrofolate reductase (MTHFR) C677T mutation in Turkish patients with thrombosis.
Balta G; Gürgey A
Turk J Pediatr; 1999; 41(2):197-9. PubMed ID: 10770658
[TBL] [Abstract][Full Text] [Related]
31. 5,10-Methylenetetrahydrofolate reductase 677C-->T and 1298A-->C mutations are genetic determinants of elevated homocysteine.
Castro R; Rivera I; Ravasco P; Jakobs C; Blom HJ; Camilo ME; de Almeida IT
QJM; 2003 Apr; 96(4):297-303. PubMed ID: 12651974
[TBL] [Abstract][Full Text] [Related]
32. Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke.
Barbagallo M; Pavone P; Incorpora G; Domenico Praticò A; Romantshik O; Friso S; Spalice A; Nicita F; Polizzi A; Ruggieri M; Iannetti P
Childs Nerv Syst; 2009 Mar; 25(3):361-5. PubMed ID: 18958479
[TBL] [Abstract][Full Text] [Related]
33. Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.
Fekih-Mrissa N; Mrad M; Klai S; Mansour M; Nsiri B; Gritli N; Mrissa R
J Stroke Cerebrovasc Dis; 2013 May; 22(4):465-9. PubMed ID: 23642756
[TBL] [Abstract][Full Text] [Related]
34. Transient ischemic attacks in a child with post-varicella arteriopathy and MTHFR homozigotic mutation C677T.
Beleza P; Fernandes J; Afonso A; Silva H; Jordão MJ
Arq Neuropsiquiatr; 2008 Jun; 66(2A):256-8. PubMed ID: 18545796
[No Abstract] [Full Text] [Related]
35. Homozygous thermolabile methylenetetrahydrofolate reductase in schizophrenia-like psychosis.
Regland B; Germgård T; Gottfries CG; Grenfeldt B; Koch-Schmidt AC
J Neural Transm (Vienna); 1997; 104(8-9):931-41. PubMed ID: 9451725
[TBL] [Abstract][Full Text] [Related]
36. Family history, plasma homocysteine, and age at onset of symptoms of myocardial ischemia in patients with different methylenetetrahydrofolate reductase genotypes.
Mager A; Koren-Morag N; Shohat M; Harell D; Battler A
Am J Cardiol; 2005 Jun; 95(12):1420-4. PubMed ID: 15950563
[TBL] [Abstract][Full Text] [Related]
37. Homocystinuria due to 5,10-methylenetetrahydrofolate reductase deficiency revealed by stroke in adult siblings.
Visy JM; Le Coz P; Chadefaux B; Fressinaud C; Woimant F; Marquet J; Zittoun J; Visy J; Vallat JM; Haguenau M
Neurology; 1991 Aug; 41(8):1313-5. PubMed ID: 1866027
[TBL] [Abstract][Full Text] [Related]
38. Hyperhomocysteinemia and the methylenetetrahydrofolate reductase 677C-T mutation in patients under 50 years of age affected by central retinal vein occlusion.
Di Crecchio L; Parodi MB; Sanguinetti G; Iacono P; Ravalico G
Ophthalmology; 2004 May; 111(5):940-5. PubMed ID: 15121372
[TBL] [Abstract][Full Text] [Related]
39. Maternal vitamin use, infant C677T mutation in MTHFR, and isolated cleft palate risk.
Shaw GM; Todoroff K; Finnell RH; Rozen R; Lammer EJ
Am J Med Genet; 1999 Jul; 85(1):84-5. PubMed ID: 10377018
[No Abstract] [Full Text] [Related]
40. [Molecular genetics of the remethylation of homocysteine].
Chango A; Parrot-Roulaud F; Nicolas J
Ann Biol Clin (Paris); 1999; 57(1):37-42. PubMed ID: 9920965
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]