151 related articles for article (PubMed ID: 11480782)
1. The methylene tetrahydrofolate reductase (C677T) mutation as a potential risk factor for avascular necrosis in sickle cell disease.
Kutlar A; Kutlar F; Turker I; Tural C
Hemoglobin; 2001 May; 25(2):213-7. PubMed ID: 11480782
[TBL] [Abstract][Full Text] [Related]
2. Inherited DNA mutations contributing to thrombotic complications in patients with sickle cell disease.
Zimmerman SA; Ware RE
Am J Hematol; 1998 Dec; 59(4):267-72. PubMed ID: 9840906
[TBL] [Abstract][Full Text] [Related]
3. Prothrombin mutant, factor V Leiden, and thermolabile variant of methylenetetrahydrofolate reductase among patients with sickle cell disease in Brazil.
Andrade FL; Annichino-Bizzacchi JM; Saad ST; Costa FF; Arruda VR
Am J Hematol; 1998 Sep; 59(1):46-50. PubMed ID: 9723576
[TBL] [Abstract][Full Text] [Related]
4. Frequency of the 677 C-->T mutation of the methylenetetrahydrofolate reductase gene among Kuwaiti sickle cell disease patients.
Adekile AD; Kutlar F; Haider MZ; Kutlar A
Am J Hematol; 2001 Apr; 66(4):263-6. PubMed ID: 11279637
[TBL] [Abstract][Full Text] [Related]
5. Correlation of the C677T MTHFR genotype with homocysteine levels in children with sickle cell disease.
Balasa VV; Gruppo RA; Gartside PS; Kalinyak KA
J Pediatr Hematol Oncol; 1999; 21(5):397-400. PubMed ID: 10524453
[TBL] [Abstract][Full Text] [Related]
6. The methylenetetrahydrofolate reductase gene C677T mutant and ischemic stroke in sickle cell disease.
Driscoll MC; Prauner R
Thromb Haemost; 1999 Dec; 82(6):1780-1. PubMed ID: 10613678
[No Abstract] [Full Text] [Related]
7. Incidence of thrombophilia in patients with Gaucher disease.
Elstein D; Renbaum P; Levy-Lahad E; Zimran A
Am J Med Genet; 2000 Dec; 95(5):429-31. PubMed ID: 11146461
[TBL] [Abstract][Full Text] [Related]
8. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.
Gemmati D; Serino ML; Trivellato C; Fiorini S; Scapoli GL
Haematologica; 1999 Sep; 84(9):824-8. PubMed ID: 10477457
[TBL] [Abstract][Full Text] [Related]
9. Methylene tetrahydrofolate reductase C677T genotype and stroke.
Salooja N; Catto A; Carter A; Tudenham EG; Grant PJ
Clin Lab Haematol; 1998 Dec; 20(6):357-61. PubMed ID: 9951581
[TBL] [Abstract][Full Text] [Related]
10. The 677C-->T mutation of the methylene-tetrahydrofolate reductase gene in the pathogenesis of osteonecrosis of the femoral head.
Zalavras CG; Malizos KN; Dokou E; Vartholomatos G
Haematologica; 2002 Jan; 87(1):111-2. PubMed ID: 11801474
[No Abstract] [Full Text] [Related]
11. Plasma folate, vitamin B(12), and total homocysteine and homozygosity for the C677T mutation of the 5,10-methylene tetrahydrofolate reductase gene in patients with Alzheimer's dementia. A case-control study.
Postiglione A; Milan G; Ruocco A; Gallotta G; Guiotto G; Di Minno G
Gerontology; 2001; 47(6):324-9. PubMed ID: 11721146
[TBL] [Abstract][Full Text] [Related]
12. The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.
Moreira Neto F; Lourenço DM; Noguti MA; Morelli VM; Gil IC; Beltrão AC; Figueiredo MS
Braz J Med Biol Res; 2006 Oct; 39(10):1291-5. PubMed ID: 16906320
[TBL] [Abstract][Full Text] [Related]
13. High frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene in Northern Italy.
Sacchi E; Tagliabue L; Duca F; Mannucci PM
Thromb Haemost; 1997 Aug; 78(2):963-4. PubMed ID: 9268207
[No Abstract] [Full Text] [Related]
14. The VITA project: C677T mutation in the methylene-tetrahydrofolate reductase gene and risk of venous thromboembolism.
Tosetto A; Missiaglia E; Frezzato M; Rodeghiero F
Br J Haematol; 1997 Jun; 97(4):804-6. PubMed ID: 9217179
[TBL] [Abstract][Full Text] [Related]
15. Prevalence of factor V G1691A (Leiden), prothrombin G20210A, and methylene tetrahydrofolate reductase C677T thrombophilic mutations in children with inflammatory bowel disease.
Kader HA; Berman WF; Al-Seraihy AS; Ware RE; Ulshen MH; Treem WR
J Pediatr Gastroenterol Nutr; 2002 Nov; 35(5):629-35. PubMed ID: 12454577
[TBL] [Abstract][Full Text] [Related]
16. The C677T mutation in the methylene tetrahydrofolate reductase gene increases serum uric acid in elderly men.
Zuo M; Nishio H; Lee MJ; Maejima K; Mimura S; Sumino K
J Hum Genet; 2000; 45(4):257-62. PubMed ID: 10944859
[TBL] [Abstract][Full Text] [Related]
17. C677T mutation in the methylene tetrahydrofolate reductase gene as a risk factor for venous thrombotic disease in Austrian patients.
Seinost G; Renner W; Brodmann M; Winkler M; Köppel H; Pilger E
Thromb Res; 2000 Dec; 100(5):405-7. PubMed ID: 11150582
[No Abstract] [Full Text] [Related]
18. Factor V Leiden and thermolabile methylenetetrahydrofolate reductase in extreme old age.
Rees DC; Liu YT; Cox MJ; Elliott P; Wainscoat JS
Thromb Haemost; 1997 Nov; 78(5):1357-9. PubMed ID: 9408019
[TBL] [Abstract][Full Text] [Related]
19. Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
Belhaj Nefissi R; Doggui R; Ouali F; Messaoud T; Gritli N
Hemoglobin; 2018 Mar; 42(2):96-102. PubMed ID: 30200836
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]