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Items: 1 to 20 of 134

1.

Prevalence of the MTHFR C677T Mutation in Fertile and Infertile Women.

Soligo AG, Barini R, Annichino-Bizzacchi JM.

Rev Bras Ginecol Obstet. 2017 Dec;39(12):659-662. doi: 10.1055/s-0037-1606289. Epub 2017 Aug 28.

2.

Successful conservative treatment of myocardial infarction in a teenager with MTHFR mutation.

Lahiri S, Cuglievan B, Gutierrez JL, Pefkarou A.

Int J Cardiol Heart Vasc. 2017 Apr 13;15:24-25. doi: 10.1016/j.ijcha.2017.03.005. eCollection 2017 Jun. No abstract available.

3.

Early Carotid Occlusion After Endarterectomy in a Patient With a Mutation for MTHFR A1298C Polymorphism.

Vidale S, Bellocchi S, Casiraghi P, Caronno R, Arnaboldi M.

Neurologist. 2017 May;22(3):95-97. doi: 10.1097/NRL.0000000000000120.

PMID:
28471900
4.

Successful management of hereditary angioedema during pregnancy in a patient with heterozygous MTHFR mutation.

Martinez Saguer I, Escuriola Ettingshausen C.

Ann Allergy Asthma Immunol. 2017 Jun;118(6):734-735. doi: 10.1016/j.anai.2017.04.001. Epub 2017 Apr 29. No abstract available.

PMID:
28465053
5.

Human MTHFR-G1793A transition may be a protective mutation against male infertility: a genetic association study and in silico analysis.

Karimian M, Hosseinzadeh Colagar A.

Hum Fertil (Camb). 2017 Mar 7:1-9. doi: 10.1080/14647273.2017.1298161. [Epub ahead of print]

PMID:
28270024
6.

The effect of the MTHFR C677T mutation on athletic performance and the homocysteine level of soccer players and sedentary individuals.

Dinç N, Yücel SB, Taneli F, Sayın MV.

J Hum Kinet. 2016 Jul 2;51:61-69. doi: 10.1515/hukin-2015-0171. eCollection 2016 Jun 1.

7.

The MTHFR C677T mutation is not a risk factor recognized for HBV-related HCC in a population with a high prevalence of this genetic marker.

Jiao X, Luo Y, Yang B, Jing L, Li Y, Liu C, Jing X, Wang F, Wang Y, Du Z, Gao Y.

Infect Genet Evol. 2017 Apr;49:66-72. doi: 10.1016/j.meegid.2017.01.008. Epub 2017 Jan 7.

PMID:
28082187
8.

Heterozygous MTHFR A1298C Mutation causing Cerebral Venous Sinus Thrombosis.

Shah JH, Salagre KD, Sahay RN, Anand A.

J Assoc Physicians India. 2016 Nov;64(11):76-77.

PMID:
27805340
9.

Characterization of a Rare Nonpathogenic Methylenetetrahydrofolatereductase (MTHFR) Gene Mutation p.Lys215del in a Southern Italian family.

Palmirotta R, Lovero D, Silvestris E, Simone V, Lanotte L, Quaresmini D, Silvestris F.

Hum Mutat. 2017 Jan;38(1):120-121. doi: 10.1002/humu.23132. Epub 2016 Oct 21. No abstract available.

PMID:
27768236
10.

Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis.

Giuffrè M, Verso CL, Serra G, Moceri G, Cimador M, Corsello G; Study Group of Neonatal Infectious Diseases Affiliated to the Italian Society of Neonatology.

Am J Perinatol. 2016 Sep;33(11):1099-103. doi: 10.1055/s-0036-1586102. Epub 2016 Sep 7.

PMID:
27603544
11.

Factor V Leiden, Prothrombin and MTHFR Mutation in Patients with Preeclamsia, Intrauterine Growth Restriction and Placental Abruption.

Livrinova V, Lega MH, Dimcheva AH, Samardziski I, Isjanovska R.

Open Access Maced J Med Sci. 2015 Dec 15;3(4):590-4. doi: 10.3889/oamjms.2015.099. Epub 2015 Sep 18.

12.

TGFBR2 mutation and MTHFR-C677T polymorphism in a Mexican mestizo population with cervico-cerebral artery dissection.

Ruiz-Franco A, Barboza MA, Jara-Prado A, Canizales-Quinteros S, Leon-Mimila P, Arguelles-Morales N, Vargas-González JC, Quiroz-Compean A, Arauz A.

J Neurol. 2016 Jun;263(6):1066-73. doi: 10.1007/s00415-016-8101-8. Epub 2016 Mar 26.

PMID:
27017342
13.

Diabetic neuropathy is not associated with homocysteine, folate, vitamin B12 levels, and MTHFR C677T mutation in type 2 diabetic outpatients taking metformin.

Russo GT, Giandalia A, Romeo EL, Scarcella C, Gambadoro N, Zingale R, Forte F, Perdichizzi G, Alibrandi A, Cucinotta D.

J Endocrinol Invest. 2016 Mar;39(3):305-14. doi: 10.1007/s40618-015-0365-9. Epub 2015 Aug 2.

PMID:
26233336
14.

Renal transplantation experience in a patient with factor V Leiden homozygous, MTHFR C677T heterozygous, and PAI heterozygous mutation.

Gülhan B, Tavil B, Gümrük F, Aki TF, Topaloglu R.

Pediatr Transplant. 2015 Aug;19(5):E126-9. doi: 10.1111/petr.12526. Epub 2015 May 21.

PMID:
25996881
15.

MTHFR (C677T) polymorphism and PR (PROGINS) mutation as genetic factors for preterm delivery, fetal death and low birth weight: A Northeast Indian population based study.

Tiwari D, Bose PD, Das S, Das CR, Datta R, Bose S.

Meta Gene. 2015 Jan 31;3:31-42. doi: 10.1016/j.mgene.2014.12.002. eCollection 2015 Feb.

16.
17.

Cerebral ultrasound abnormalities in offsprings of women with C677T homozygous mutation in the MTHFR gene: a prospective study.

Pogliani L, Cerini C, Penagini F, Duca P, Mameli C, Zuccotti GV.

World J Pediatr. 2015 May;11(2):134-40. doi: 10.1007/s12519-014-0490-0. Epub 2014 Jun 28.

PMID:
24974211
18.

Hyperhomocysteinaemia, low folate concentrations and MTHFR C677T mutation in abdominal aortic aneurysm.

Cao H, Hu X, Zhang Q, Li J, Liu B, Wang J, Shao Y, Zhang Z, Liu C, Hu H, Zhang J, Xin S.

Vasa. 2014 May;43(3):181-8. doi: 10.1024/0301-1526/a000347.

PMID:
24797049
19.

[Central nervous system malformations and the presence of the MTHFR-C677T mutation in fetal blood].

Simoni RZ, Couto E, Barini R, Heinrich-Moçouçah J, Bragança WO, Couto ER, Bizzachi JM.

Rev Bras Ginecol Obstet. 2013 Oct;35(10):436-41. Portuguese.

20.

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