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There are 7739920 results for: content related to: Prothrombin 20210 G[RIGHTWARDS ARROW]A, MTHFR C677T mutations in women with venous thromboembolism associated with pregnancy

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    Journal of Thrombosis and Haemostasis

    Volume 3, Issue s1, August 2005, Pages: H01–SYM90,

    Version of Record online : 6 SEP 2013, DOI: 10.1111/j.1538-7836.2005.03000.x

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    Journal of Thrombosis and Haemostasis

    Volume 3, Issue s1, August 2005, Pages: P0001–P2386,

    Version of Record online : 9 SEP 2013, DOI: 10.1111/j.1538-7836.2005.0300c.x

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    Journal of Thrombosis and Haemostasis

    Volume 7, Issue s2, July 2009, Pages: 317–1168,

    Version of Record online : 15 JUN 2009, DOI: 10.1111/j.1538-7836.2009.03473_2.x

  4. Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients?

    Asia-Pacific Journal of Clinical Oncology

    Volume 8, Issue 3, September 2012, Pages: e34–e41, Metin OZKAN, Serdar SIVGIN, Ismail KOCYIGIT, Funda EMIROGULLARI, Mustafa DIKILITAS, Leylagul KAYNAR, Yusuf OZKUL and Ozlem ER

    Version of Record online : 15 MAY 2012, DOI: 10.1111/j.1743-7563.2012.01536.x

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    Journal of Thrombosis and Haemostasis

    Volume 5, Issue S2, July 2007, Pages: P-W-401–P-W-701,

    Version of Record online : 13 FEB 2014, DOI: 10.1111/j.1538-7836.2007.tb00035.x

  6. Association of Mycobacterium infections in patients with Mendelian Susceptibility to Mycobacterium Disease (MSMD) with Venous Thromboembolism

    Microbiology and Immunology

    Accepted manuscript online: 30 SEP 2016, Maryam Alinejad Dizaj, Seyed Alireza Mahdaviani, Payam Tabarsi, Hamed Ahari, Ahmad Ebrahimi, Seyed Alireza Nadji, Habib Emami and Esmaeil Mortaz

    DOI: 10.1111/1348-0421.12442

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    Journal of Thrombosis and Haemostasis

    Volume 13, Issue S2, June 2015, Pages: 1–997,

    Version of Record online : 3 JUN 2015, DOI: 10.1111/jth.12993

  8. Frequency of selected thrombophilias in women with placental abruption

    Australian and New Zealand Journal of Obstetrics and Gynaecology

    Volume 47, Issue 4, August 2007, Pages: 297–301, Martin PROCHÁZKA, Marek LUBUŠKÝ, Luděk SLAVÍK, Petr HRACHOVEC, Petr ZIELINA, Milan KUDELA and Pelle G. LINDQVIST

    Version of Record online : 11 JUL 2007, DOI: 10.1111/j.1479-828X.2007.00741.x

  9. Genetic polymorphisms of methylenetetrahydrofolate reductase (MTHFR) and methionine synthase reductase (MTRR) in ethnic populations in Texas; a report of a novel MTHFR polymorphic site, G1793A

    American Journal of Medical Genetics

    Volume 107, Issue 2, 15 January 2002, Pages: 162–168, Peter L. Rady, Sylvia Szucs, James Grady, S. David Hudnall, Leonard H. Kellner, Harold Nitowsky, Stephen K. Tyring and Reuben K. Matalon

    Version of Record online : 26 DEC 2001, DOI: 10.1002/ajmg.10122

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    Abstracts: Turkish Society of Molecular Medicine, Third International Congress of Molecular Medicine, May 5–8, 2009, Istanbul, Turkey

    IUBMB Life

    Volume 61, Issue 3, March 2009, Pages: 273–389, Prof. Dr. Turgay Isbir

    Version of Record online : 25 FEB 2009, DOI: 10.1002/iub.183

  11. Portal vein thrombosis in Egyptian patients with liver cirrhosis: Role of methylenetetrahydrofolate reductase C677T gene mutation

    Hepatology Research

    Volume 40, Issue 5, May 2010, Pages: 486–493, Mamdouh Ahmed Gabr, Sahar Saad El-Din Bessa and Enas Arafa El-Zamarani

    Version of Record online : 30 MAR 2010, DOI: 10.1111/j.1872-034X.2010.00628.x

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    Methylenetetrahydrofolate reductase C677T gene mutation and hyperhomocysteinemia in Budd–Chiari syndrome and portal vein thrombosis: A systematic review and meta-analysis of observational studies

    Hepatology Research

    Volume 44, Issue 14, December 2014, Pages: E480–E498, Xingshun Qi, Zhiping Yang, Valerio De Stefano and Daiming Fan

    Version of Record online : 20 MAY 2014, DOI: 10.1111/hepr.12348

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    Association of factor V Leiden, Janus kinase 2, prothrombin, and MTHFR mutations with primary Budd–Chiari syndrome in Egyptian patients

    Journal of Gastroenterology and Hepatology

    Volume 31, Issue 1, January 2016, Pages: 235–240, Hatem M El Sebay, Manal A Safan, Ashraf A Daoud, Safaa I Tayel, Mohamed A Nouh and Shymaa El Shafie

    Version of Record online : 30 DEC 2015, DOI: 10.1111/jgh.13066

  14. Interrelationships among genetic C677T polymorphism of 5,10-methylenetetrahydrofolate reductase, biochemical folate status, and lymphocytic p53 oxidative damage in association with tumor malignancy and survivals of patients with hepatocellular carcinoma

    Molecular Nutrition & Food Research

    Volume 58, Issue 2, February 2014, Pages: 329–342, Chang-Sheng Kuo, Chi-Yun Huang, Hsing-Tao Kuo, Chin-Pao Cheng, Chien-Hung Chen, Chin-Li Lu, Feili-Lo Yang and Rwei-Fen Syu Huang

    Version of Record online : 29 AUG 2013, DOI: 10.1002/mnfr.201200479

  15. Combined Thrombophilic Mutations in Women with Unexplained Recurrent Miscarriage

    American Journal of Reproductive Immunology

    Volume 57, Issue 2, February 2007, Pages: 133–141, Alexandros Sotiriadis, George Vartholomatos, Matthaios Pavlou, Nicolaos Kolaitis, Leucothea Dova, Theodor Stefos, Evangelos Paraskevaidis and Sophia N. Kalantaridou

    Version of Record online : 8 JAN 2007, DOI: 10.1111/j.1600-0897.2006.00454.x

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    Evidence that interactive effects of COMT and MTHFR moderate psychotic response to environmental stress

    Acta Psychiatrica Scandinavica

    Volume 125, Issue 3, March 2012, Pages: 247–256, O. Peerbooms, B. P. F. Rutten, D. Collip, M. Lardinois, T. Lataster, V. Thewissen, S. Mafi Rad, M. Drukker, G. Kenis, J. van Os, I. Myin-Germeys and R. van Winkel

    Version of Record online : 30 NOV 2011, DOI: 10.1111/j.1600-0447.2011.01806.x

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

    Pediatric Transplantation

    Volume 19, Issue 5, August 2015, Pages: E126–E129, Bora Gülhan, Betül Tavil, Fatma Gümrük, Tuncay F. Aki and Rezan Topaloglu

    Version of Record online : 21 MAY 2015, DOI: 10.1111/petr.12526

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    Association analysis of the COMT/MTHFR genes and geriatric depression: An MRI study of the putamen

    International Journal of Geriatric Psychiatry

    Volume 24, Issue 8, August 2009, Pages: 847–855, Chih-Chuan Pan, Douglas R. McQuoid, Warren D. Taylor, Martha E. Payne, Allison Ashley-Koch and David C. Steffens

    Version of Record online : 23 FEB 2009, DOI: 10.1002/gps.2206

  19. Methylenetetrahydrofolate reductase homozygosis and low-density lipoproteins in patients with genotype 1 chronic hepatitis C

    Journal of Viral Hepatitis

    Volume 19, Issue 7, July 2012, Pages: 465–472, S. Petta, C. Bellia, A. Mazzola, D. Cabibi, C. Cammà, A. Caruso, V. Di Marco, A. Craxì and M. Ciaccio

    Version of Record online : 28 NOV 2011, DOI: 10.1111/j.1365-2893.2011.01557.x

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    Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion

    Acta Ophthalmologica Scandinavica

    Volume 78, Issue 3, June 2000, Pages: 340–343, J. Larsson, B. Hultberg and A. Hillarp

    Version of Record online : 24 DEC 2001, DOI: 10.1034/j.1600-0420.2000.078003340.x