Sage Journals: Discover world-class research

Retricted access

Case report

First published 2012-5

Myocardial Infarction in a Newborn Heterozygous for the MTHFR C677T Mutation

Amy B. Clark, Theophil A. Stokes, Henry F. Krous [...]

Pediatric and Developmental Pathology

Retricted access

Research article

First published 2008-09

Bilateral Transverse Sinus Thrombosis Secondary to a Homozygous C677T MTHFR Gene Mutation

Ziad M. Kanaan, Rami Mahfouz, Ali Taher [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Brief report

First published 2003-09

High Incidence of Two Methylenetetrahydrofolate Reductase Mutations (C677T and A1298C) in Hispanics

Dondapati Chowdary, Deanna Streck, Marvin N. Schwalb [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Brief report

First published 2000-09

Ethnic Differences in the Frequency of the C677T Mutation in the Methylenetetrahydrofolate Reductase ( MTHFR ) Gene in Healthy Israeli Populations

Rivka Dresner Pollak, Yechiel Friedlander, Arthur Pollak [...]

Genetic Testing and Molecular Biomarkers

Retricted access

Other

First published 2002-01

Presence of the 5,10-Methylenetetrahydrofolate Reductase C677T Mutation in Puerto Rican Patients With Neural Tube Defects

Lourdes Garcia-Fragoso, Inés García-García, Alberto de la Vega [...]

Journal of Child Neurology

Free access

Research article

First published 2006-10

Stromelysin-1 5A/6A and eNOS T-786C Polymorphisms,MTHFR C677T and A1298C Mutations,and Cigarette-Cannabis Smoking: A Pilot,Hypothesis-Generating Study of Gene-Environment Pathophysiological Associations With Buerger’s Disease

Charles J. Glueck, Mofiz Haque, Magdalena Winarska [...]

Clinical and Applied Thrombosis/Hemostasis

Open access

Research article

First published 2019

The Role of Factor V Leiden,Prothrombin G20210A,and MTHFR C677T Mutations in Neonatal Cerebral Sinovenous Thrombosis

Maria Garrido-Barbero, Juan Arnaez, Begoña Loureiro [...]

Clinical and Applied Thrombosis/Hemostasis

Free access

Research article

First published 2015-3

The Prevalence of Factor V Leiden (G1691A) and Methylenetetrahydrofolate Reductase C677T Mutations in Sickle Cell Disease in Western India

Harshada K. Kangne, Farah F. Jijina, Yazdi M. Italia [...]

Clinical and Applied Thrombosis/Hemostasis

Free access

Research article

First published 2007-04

The Frequency of Factor V Leiden and Concomitance of Factor V Leiden With Prothrombin G20210A Mutation and Methylene Tetrahydrofolate Reductase C677T Gene Mutation in Healthy Population of Denizli,Aegean Region of Turkey

Sibel Kabukcu, Nazan Keskin, Ali Keskin [...]

Clinical and Applied Thrombosis/Hemostasis

Retricted access

Other

First published 2007-04

Moya Moya Syndrome in a Child With Pyruvate Kinase Deficiency and Combined Prothrombotic Factors

Angeliki Skardoutsou, Konstantinos A. Voudris, Sotiria Mastroyianni [...]

Journal of Child Neurology

Search results