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    Results: 1 to 20 of 89

    2.

    [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss]

    Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.

    Akush Ginekol (Sofiia). 2007;46(7):10-6. Bulgarian. PMID: 18333414 [PubMed - indexed for MEDLINE]Related articles

    3.

    [Genetic variant C677T in the MTHFR in women with recurrent early fetal loss]

    Ivanov P, Kovacheva K, Komsa-Penkova R, Konova E, Simeonova M, Popov I, Gecheva S, Bozhinova S, Tanchev S, Tsafarov M.

    Akush Ginekol (Sofiia). 2007;46(4):19-22. Bulgarian. PMID: 17974190 [PubMed - indexed for MEDLINE]Related articles

    4.

    [Relationship between methylenetetrahydrofolate reductase polymorphism and homocysteine levels in women with recurrent pregnancy loss: a nutrigenetic perspective]

    Cardona H, Cardona-Maya W, Gómez JG, Castañeda S, Gómez JM, Bedoya G, Alvarez L, Torres JD, Tobón LI, Cadavid A.

    Nutr Hosp. 2008 May-Jun;23(3):277-82. Spanish. PMID: 18560705 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Homozygous MTHFR C677T gene mutation and recurrent stroke in an infant.

    Garoufi AJ, Prassouli AA, Attilakos AV, Voudris KA, Katsarou ES.

    Pediatr Neurol. 2006 Jul;35(1):49-51.PMID: 16814086 [PubMed - indexed for MEDLINE]Related articles

    6.

    Genetic thrombophilias and intrauterine growth restriction: a meta-analysis.

    Facco F, You W, Grobman W.

    Obstet Gynecol. 2009 Jun;113(6):1206-16.PMID: 19461414 [PubMed - indexed for MEDLINE]Related articles

    7.

    Peripheral arterial disease and methylenetetrahydrofolate reductase (MTHFR) C677T mutations: A case-control study and meta-analysis.

    Khandanpour N, Willis G, Meyer FJ, Armon MP, Loke YK, Wright AJ, Finglas PM, Jennings BA.

    J Vasc Surg. 2009 Mar;49(3):711-8. Epub 2009 Jan 21. Review.PMID: 19157768 [PubMed - indexed for MEDLINE]Related articles

    9.

    Recurrent abortions in Asian Indians: no role of factor V Leiden Hong Kong/Cambridge mutation and MTHFR polymorphism.

    Biswas A, Choudhry P, Mittal A, Meena A, Ranjan R, Choudhry VP, Saxena R.

    Clin Appl Thromb Hemost. 2008 Jan;14(1):102-4. Epub 2007 Dec 26.PMID: 18160599 [PubMed - indexed for MEDLINE]Related articles

    10.

    Inherited thrombophilia screening in Greek women with recurrent fetal loss.

    Mougiou A, Androutsopoulos G, Karakantza M, Theodori E, Decavalas G, Zoumbos N.

    Clin Exp Obstet Gynecol. 2008;35(3):172-4.PMID: 18754285 [PubMed - indexed for MEDLINE]Related articles

    11.

    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. Epub 2008 Oct 29.PMID: 18958479 [PubMed - indexed for MEDLINE]Related articles

    12.

    Bilateral transverse sinus thrombosis secondary to a homozygous C677T MTHFR gene mutation.

    Kanaan ZM, Mahfouz R, Taher A, Sawaya RA.

    Genet Test. 2008 Sep;12(3):363-5.PMID: 18666857 [PubMed - indexed for MEDLINE]Related articles

    13.

    Thrombophilia and unexplained pregnancy loss in Indian patients.

    Vora S, Shetty S, Salvi V, Satoskar P, Ghosh K.

    Natl Med J India. 2008 May-Jun;21(3):116-9.PMID: 19004141 [PubMed - indexed for MEDLINE]Related articles

    14.

    Comparison of thrombophilic gene mutations among patients experiencing recurrent miscarriage and deep vein thrombosis.

    Coulam CB, Wallis D, Weinstein J, DasGupta DS, Jeyendran RS.

    Am J Reprod Immunol. 2008 Nov;60(5):426-31.PMID: 18803625 [PubMed - indexed for MEDLINE]Related articles

    15.

    ACE and MTHFR gene polymorphisms in unexplained recurrent pregnancy loss.

    Vettriselvi V, Vijayalakshmi K, Paul SF, Venkatachalam P.

    J Obstet Gynaecol Res. 2008 Jun;34(3):301-6.PMID: 18588608 [PubMed - indexed for MEDLINE]Related articles

    16.

    Genotypes of the C677T and A1298C polymorphisms of the MTHFR gene as a cause of human spontaneous embryo loss.

    Callejón G, Mayor-Olea A, Jiménez AJ, Gaitán MJ, Palomares AR, Martínez F, Ruiz M, Reyes-Engel A.

    Hum Reprod. 2007 Dec;22(12):3249-54. Epub 2007 Oct 25.PMID: 17965025 [PubMed - indexed for MEDLINE]Related articlesFree article

    17.

    Synergistic effect of methyltetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphism as risk modifiers of pediatric acute lymphoblastic leukemia.

    Kamel AM, Moussa HS, Ebid GT, Bu RR, Bhatia KG.

    J Egypt Natl Canc Inst. 2007 Jun;19(2):96-105.PMID: 19034339 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    Genetic polymorphisms of methylenetetrahydrofolate reductase and susceptibility to colorectal cancer.

    Cao HX, Gao CM, Takezaki T, Wu JZ, Ding JH, Liu YT, Li SP, Su P, Cao J, Hamajima N, Tajima K.

    Asian Pac J Cancer Prev. 2008 Apr-Jun;9(2):203-8.PMID: 18712959 [PubMed - indexed for MEDLINE]Related articles

    19.

    Plasma total homocysteine levels and methylenetetrahydrofolate reductase gene polymorphism in patients with type 2 diabetes mellitus.

    Soares AL, Fernandes AP, Cardoso JE, Sousa MO, Lasmar MC, Novelli BA, Lages GF, Dusse LM, Vieira LM, Lwaleed BA, Carvalho MG.

    Pathophysiol Haemost Thromb. 2008;36(5):275-81. Epub 2009 Dec 9.PMID: 19996639 [PubMed - indexed for MEDLINE]Related articles

    20.

    Risk of colorectal cancer associated with the C677T polymorphism in 5,10-methylenetetrahydrofolate reductase in Portuguese patients depends on the intake of methyl-donor nutrients.

    Guerreiro CS, Carmona B, Gonçalves S, Carolino E, Fidalgo P, Brito M, Leitão CN, Cravo M.

    Am J Clin Nutr. 2008 Nov;88(5):1413-8.PMID: 18996879 [PubMed - indexed for MEDLINE]Related articlesFree article

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