HuGE Literature Finder
Records 1-30
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Thrombophilic Risk of Factor V Leiden, Prothrombin G20210A, MTHFR, and Calreticulin Mutations in Essential Thrombocythemia Egyptian Patients.
Advances in hematology 2020 2020 7695129. El-Ghonemy Mohamed S, El Sharawy Solafa, Fahmi Maryan Waheeb, El-Ashwah Shaimaa, Denewer May, El-Baiomy M |
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Relationship between genetic polymorphism of MTHFR C677T and lower extremities deep venous thrombosis.
Hematology (Amsterdam, Netherlands) 2019 Dec 24 (1): 108-111. Xu Jiasheng, Li Kexin, Zhou Weim |
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Investigation of potential biomarkers for thrombosis related diseases in Turkish Cypriot population.
International journal of biological macromolecules 2019 Mar 124 515-518. Ergoren M C, Tulay |
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Correlations between methylenetetrahydrofolate reductase gene polymorphisms and venous thromboembolism: A meta-analysis of 99 genetic association studies.
European journal of preventive cardiology 2019 Jan 26 (2): 120-134. Zeng Juan, Zeng Qingh |
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Impact of maternal methylenetetrahydrofolate reductase C677T polymorphism on intervillous and decidual pathology with pregnancy loss.
The journal of obstetrics and gynaecology research 2018 Aug . Mehandjiev Tzvetozar R, Tenno Nodoka M, Nakura Yukiko, Georgiev Tzanko P, Minekawa Ryoko, Wakimoto Tetsu, Mimura Kazuya, Nakayama Masahiro, Kawakami Kanae, Kanagawa Takeshi, Tomimatsu Takuji, Fujita Tomio, Onouchi Yoshihiro, Takeuchi Makoto, Kimura Tadashi, Yanagihara Ita |
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Frequency and characteristics associated with inherited thrombophilia in patients with intracranial dural arteriovenous fistula.
Journal of neurosurgery 2018 Apr 1-5. LaHue Sara C, Kim Helen, Pawlikowska Ludmila, Nelson Jeffrey, Cooke Daniel L, Hetts Steven W, Singh Vinee |
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Factor V Leiden G1691A, Prothrombin G20210A, and MTHFR C677T and A1298C Mutations in Patients With Sickle Cell Disease in Tunisia.
Hemoglobin 2018 Mar 42 (2): 96-102. Belhaj Nefissi Rim, Doggui Radhouene, Ouali Faida, Messaoud Taieb, Gritli Nasreddi |
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Identification of genetic risk factors associated with ischaemic stroke in young Mexican patients.
Neurologia (Barcelona, Spain) 2018 Mar . Jiménez-González M C, Santiago-Germán D, Castillo-Henkel E F, Alvarado-Moreno J A, Hernández-Juárez J, Leaños-Miranda A, Majluf-Cruz A, Isordia-Salas |
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High prevalence of factor V Leiden and prothrombin G20101A mutations in Kashmiri patients with venous thromboembolism.
Gene 2018 Feb . Shafia Syed, Zargar Mahrukh H, Khan Nabeela, Ahmad Rehana, Shah Zafar Amin, Asimi Ravo |
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Methylenetetrahydrofolate Reductase Gene Polymorphism (C677T) as a Risk Factor for Arterial Thrombosis in Georgian Patients.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 1076029618757345. Garakanidze Sopio, Costa Elísio, Bronze-Rocha Elsa, Santos-Silva Alice, Nikolaishvili Giorgi, Nakashidze Irina, Kakauridze Nona, Glonti Salome, Khukhunaishvili Rusudan, Koridze Marina, Ahmad Sarfr |
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Polymorphisms C677T and A1298C of MTHFR Gene: Homocysteine Levels and Prothrombotic Biomarkers in Coronary and Pulmonary Thromboembolic Disease.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 1076029618780344. Lupi-Herrera Eulo, Soto-López María Elena, Lugo-Dimas Antonio de Jesús, Núñez-Martínez Marcela Elizabeth, Gamboa Ricardo, Huesca-Gómez Claudia, Sierra-Galán Lilia Mercedes, Guarner-Lans Veróni |
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Thrombophilic Gene Mutations in Relation to Different Manifestations of Venous Thromboembolism: A Single Tertiary Center Study.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Jan 24 (1): 100-106. Bezgin Tahir, Kaymaz Cihangir, Akbal Özgür, Yilmaz Fatih, Tokgöz Hacer Ceren, Özdemir Nih |
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Thrombophilic Mutations Among Patients with Sickle Cell Disease.
Clinical laboratory 2017 Nov 63 (11): 1815-1818. Nefissi Rim B, Ouali Faida, Massaoud Taieb, Gritli Nasreddi |
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Prevalence of common hereditary risk factors for thrombophilia in Somalia and identification of a novel Gln544Arg mutation in coagulation factor V.
Journal of thrombosis and thrombolysis 2017 Sep . Abdi Abshir Ali, Osman Abdimaj |
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Prevalence of 1691G>A F5, 20210G>A F2, and 677C>T MTHFR polymorphisms in Bosnian women with pregnancy loss.
Bosnian journal of basic medical sciences 2017 May . Mahmutbegovic Emir, Marjanovic Damir, Medjedovic Edin, Mahmutbegovic Nevena, Dogan Serkan, Valjevac Amina, Czerska Ewa, Pawi?ska-Matecka Anna, Madlani Agnieszka, Adler Grazy |
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Prevalence of Factor V Leiden-G1691A and MTHFR-C677T Thrombosis Gene Modifier in Iron Deficiency Anemia: A Pathophysiological Effect in Indian Isolates.
Indian journal of clinical biochemistry : IJCB 2017 Mar 32 (1): 103-105. Pandey S K, Pandey S, Mishra R M, Indurkar |
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Cilioretinal artery: Vasculogenesis might be promoted by plasminogen activator inhibitor-1 5G allele.
Ophthalmic genetics 2017 Feb 1-6. Yilmaz Sarenur, Ardagil Aylin, Akalin Ibrahim, Guzin Altinel Meltem, Dag Yasar, Kurum Esra, Koyun Efe, Ari Yaylali Sevil, Bayramlar Husey |
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Interactions among methylenetetrahydrofolate reductase (MTHFR) and cystathionine ?-synthase (CBS) polymorphisms - a cross-sectional study: multiple heterozygosis as a risk factor for higher homocysteine levels and vaso-occlusive episodes.
Genetics and molecular research : GMR 2017 Feb 16 (1): . Amaral F M, Miranda-Vilela A L, Lordelo G S, Ribeiro I F, Daldegan M B, Grisolia C |
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Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study.
Ophthalmic genetics 2017 Jan 1-5. Koylu Mehmet Talay, Kucukevcilioglu Murat, Erdurman Fazil Cuneyt, Durukan Ali Hakan, Sobac? Gungor, Torun Deniz, Tunca Yusuf, Ayyildiz Ond |
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Atherosclerotic and thrombotic genetic and environmental determinants in Egyptian coronary artery disease patients: a pilot study.
BMC cardiovascular disorders 2017 Jan 17 (1): 26. Fawzy Manal S, Toraih Eman A, Aly Nagwa M, Fakhr-Eldeen Abeer, Badran Dahlia I, Hussein Mohammad |
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A Prothrombotic Score Based on Genetic Polymorphisms of the Hemostatic System Differs in Patients with Ischemic Stroke, Myocardial Infarction, or Peripheral Arterial Occlusive Disease.
Frontiers in cardiovascular medicine 2017 4 39. Herm Juliane, Hoppe Berthold, Siegerink Bob, Nolte Christian H, Koscielny Jürgen, Haeusler Karl Geo |
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The ß-fibrinogen gene 455G/A polymorphism associated with cardioembolic stroke in atrial fibrillation with low CHA
Scientific reports 2017 12 7 (1): 17517. Hu Xiaofeng, Wang Junjun, Li Yaguo, Wu Jiong, Qiao Song, Xu Shanhu, Huang Jun, Chen Linh |
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Towards the genetic basis of cerebral venous thrombosis-the BEAST Consortium: a study protocol.
BMJ open 2016 Nov 6 (11): e012351. Cotlarciuc Ioana, Marjot Thomas, Khan Muhammad S, Hiltunen Sini, Haapaniemi Elena, Metso Tiina M, Putaala Jukka, Zuurbier Susanna M, Brouwer Matthijs C, Passamonti Serena M, Bucciarelli Paolo, Pappalardo Emanuela, Patel Tasmin, Costa Paolo, Colombi Marina, Canhão Patrícia, Tkach Aleksander, Santacroce Rosa, Margaglione Maurizio, Favuzzi Giovanni, Grandone Elvira, Colaizzo Donatella, Spengos Kostas, Arauz Antonio, Hodge Amanda, Ditta Reina, Debette Stephanie, Zedde Marialuisa, Pare Guillaume, Ferro José M, Thijs Vincent, Pezzini Alessandro, Majersik Jennifer J, Martinelli Ida, Coutinho Jonathan M, Tatlisumak Turgut, Sharma Pankaj, |
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Association of Mycobacterium infections in patients with Mendelian Susceptibility to Mycobacterium Disease (MSMD) with Venous Thromboembolism.
Microbiology and immunology 2016 Sep . Alinejad Dizaj Maryam, Mahdaviani Seyed Alireza, Tabarsi Payam, Ahari Hamed, Ebrahimi Ahmad, Nadji Seyed Alireza, Emami Habib, Mortaz Esmae |
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Genetic Risk Factors in Venous Thromboembolism.
Advances in experimental medicine and biology 2016 Sep . Hotoleanu Cristi |
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Portal Vein Thrombosis in a Preterm Newborn with Mutation of the MTHFR and PAI-1 Genes and Sepsis by Candida parapsilosis.
American journal of perinatology 2016 Sep 33 (11): 1099-103. Giuffrè Mario, Verso Clelia Lo, Serra Gregorio, Moceri Giovanni, Cimador Marcello, Corsello Giovanni, |
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The efficacy of tissue factor -603A/G and +5466A>G polimorphisms at the development of venous thromboembolism in cancer patients.
Experimental oncology 2016 Sep 38 (3): 187-90. Ero?lu A, Ceylan G G, Ozturk E, Yalcin A, Yalcin B, Karasoy |
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The Impact of Inherited Thrombophilia Types and Low Molecular Weight Heparin Treatment on Pregnancy Complications in Women with Previous Adverse Outcome.
Yonsei medical journal 2016 Sep 57 (5): 1230-5. Aracic Nada, Roje Damir, Jakus Ivana Alujevic, Bakotin Marinela, Stefanovic Vedr |
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Frequency and association of 1691 (G>A) FVL, 20210 (G>A) PT and 677 (C>T) MTHFR with deep vein thrombosis in the population of Bosnia and Herzegovina.
Balkan journal of medical genetics : BJMG 2016 Jul 19 (1): 43-50. Jusi?-Kari? A, Terzi? R, Jerki? Z, Avdi? A, Po?anin |
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Venous Thromboembolism After Knee Arthroscopy in Undiagnosed Familial Thrombophilia.
Orthopedics 2016 Jul 1-6. Jetty Vybhav, Glueck Charles J, Freiberg Richard A, Wang Pi |
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Intracardiac Thrombosis Involving All Four Cardiac Chambers after Extracardiac Membranous Oxygenation Associated with MTHFR Mutations.
The Korean journal of thoracic and cardiovascular surgery 2016 Jun 49 (3): 207-9. Kim Bong Jun, Song Seung Hwan, Shin Yu Rim, Park Han Ki, Park Young Hwan, Shin Hong |
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Potential Risk Factors Associated With Vascular Diseases in Patients Receiving Treatment for Hypertension.
Annals of laboratory medicine 2016 May 36 (3): 215-22. Kim Hyunjung, Park Joonhong, Chae Hyojin, Lee Gun Dong, Lee Sang Yoon, Lee Jong Min, Oh Yong Seog, Kim Myungshin, Kim Yongg |
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Correlation with Platelet Parameters and Genetic Markers of Thrombophilia Panel (Factor II g.20210G>A, Factor V Leiden, MTHFR (C677T, A1298C), PAI-1, ?-Fibrinogen, Factor XIIIA (V34L), Glycoprotein IIIa (L33P)) in Ischemic Strokes.
Neuromolecular medicine 2016 Mar . Tasdemir Sener, Erdem Haktan Bagis, Sahin Ibrahim, Ozel Lutfi, Ozdemir Gokhan, Eroz Recep, Tatar Abdulga |
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Hyperhomocysteinemia and MTHFR C677T polymorphism in patients with portal vein thrombosis complicating liver cirrhosis.
Thrombosis research 2016 Mar 141 189-195. Ventura Paolo, Venturelli Giorgia, Marcacci Matteo, Fiorini Massimo, Marchini Stefano, Cuoghi Chiara, Pietrangelo Antonel |
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Role of Hyperhomocysteinemia and Methylene Tetrahydrofolate Reductase C677T Polymorphism in Idiopathic Portal Vein Thrombosis.
Vascular specialist international 2016 Mar 32 (1): 6-10. Ghaznavi Habib, Soheili Zahra, Samiei Shahram, Soltanpour Mohammad Soleim |
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Variant alleles in factor V, prothrombin, plasminogen activator inhibitor-1, methylenetetrahydrofolate reductase and risk of thromboembolism in metastatic colorectal cancer patients treated with first-line chemotherapy plus bevacizumab.
The pharmacogenomics journal 2016 Mar . Falvella F S, Cremolini C, Miceli R, Nichetti F, Cheli S, Antoniotti C, Infante G, Martinetti A, Marmorino F, Sottotetti E, Berenato R, Caporale M, Colombo A, de Braud F, Di Bartolomeo M, Clementi E, Loupakis F, Pietrantonio |
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Primary thrombophilia in Mexico: a single tertiary referral hospital experience.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2016 Jan . Lacayo-Leñero Dennis, Hernández-Hernández Darinel, Valencia-Martínez Andrés, Barrales-Benítez Olga, Vargas-Ruiz Angel |
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Possible Association Between the Methylenetetrahydrofolate Reductase Gene C677T Polymorphism and Preexisting Portal Vein Thrombosis in Liver Transplant Recipients.
Experimental and clinical transplantation : official journal of the Middle East Society for Organ Transplantation 2016 06 14 (3): 313-6. Kamei Hideya, Nakamura Taro, Nagai Shunji, Ishigami Masatoshi, Hamajima Nobuyu |
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Thrombosis Related ABO, F5, MTHFR, and FGG Gene Polymorphisms in Morbidly Obese Patients.
Disease markers 2016 2016 7853424. Kupcinskiene Kristina, Murnikovaite Martyna, Varkalaite Greta, Juzenas Simonas, Trepenaitis Darius, Petereit Ruta, Maleckas Almantas, Kupcinskas Juozas, Macas Andri |
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Association of Methylenetetrahydrofolate Reductase C677T Polymorphism with Hyperhomocysteinemia and Deep Vein Thrombosis in the Iranian Population.
Vascular specialist international 2015 Dec 31 (4): 109-14. Ghaznavi Habib, Soheili Zahra, Samiei Shahram, Soltanpour Mohammad Soleim |
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Molecular and biochemical investigations of patients with intermediate or severe hyperhomocysteinemia.
Molecular genetics and metabolism 2015 Dec . Sørensen Jannie Tanderup, Gaustadnes Mette, Stabler Sally P, Allen Robert H, Mudd S Harvey, Hvas Anne-Met |
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PAI-1 4G-4G and MTHFR 677TT in non-hepatitis C virus/hepatitis B virus-related liver cirrhosis.
World journal of hepatology 2015 Dec 7 (29): 2920-6. Pasta Linda, Pasta Frances |
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Plasma homocysteine levels, methylene tetrahydrofolate reductase A1298C gene polymorphism and risk of retinal vein thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Dec . Ghaznavi Habib, Soheili Zahra, Samiei Shahram, Soltanpour Mohammad Soleim |
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Frequency of three prothrombotic polymorphisms among Syrian Population: Factor V G1691A, Prothrombin G20210A and Methylenetetrahydrofolate Reductase C677T.
Annals of human biology 2015 Nov 1-17. Jarjour Rami A, Ammar Samer, Majdalawi Ra |
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A Study on Hereditary Thrombophilia and Stroke in a Cohort from Sri Lanka.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2015 Oct . Kalpage Hasini A, Sumathipala Dulika S, Goonasekara Hemali W, Dissanayake Vajira |
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Coexistence of the 677C>T and 1298A>C MTHFR polymorphisms and its significance in the population of Polish women.
Ginekologia polska 2015 Oct 86 (10): 742-7. Wolski Hubert, Koci?cka Maria, Mrozikiewicz Aleksandra E, Barlik Magdalena, Kurzawi?ska Gra?y |
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Effects of MTHFR c.677C>T, F2 c.20210G>A and F5 Leiden Polymorphisms in Gastroschisis.
Journal of investigative surgery : the official journal of the Academy of Surgical Research 2015 Sep 1-5. Makhmudi Akhmad, Sadewa Ahmad Hamim, Aryandono Teguh, Chatterjee Sumantra, Heij Hugo A, Gunad |
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Prothrombin G20210A and methylenetetrahydrofolate reductase C677T polymorphisms in peripheral capillary nonperfusion: a case report.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Sep 26 (6): 682-4. Wathek Chaima, Mrad Meriem, Abdessalem Nadia Ben, Maalej Afef, Gritli Nasreddine, Gabsi Salem, Rannen Riadh, Fekih-Mrissa Naji |
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The Contributions of Thrombophilic Mutations to Genetic Susceptibility to Deep Venous Thrombosis in Iraqi Patients.
Genetic testing and molecular biomarkers 2015 Sep 19 (9): 500-4. Al-Allawi Nasir A S, Badi Ameer I A, Goran Musheer A, Nerweyi Farida F A, Ballo Hawar M S, Al-Mzury Najat T |
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Thrombophilia Profile in Budd-Chiari Syndrome and Splanchnic Vein Thrombosis: A Study from Western India.
The Journal of the Association of Physicians of India 2015 Sep 63 (9): 32-5. Sawant Prabha, Vashishtha Chitranshu, Nasa Mukesh, Parikh Pathik, Patel Jignesh, Agasti Anan |
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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 2015 Aug . El Sebay Hatem M, Safan Manal A, Daoud Ashraf A, Tayel Safaa I, Nouh Alaa, El Shafie Shym |
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Risk factors for thrombosis development in Mexican patients.
Annals of vascular surgery 2015 Aug . Zavala-Hernández César, Hernández-Zamora Edgar, Martínez-Murillo Carlos, Majluf-Cruz Abraham, Vela-Ojeda Jorge, García-Chávez Jaime, Reyes-Maldonado El |
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Thrombophilia and venous thromboembolism in pregnancy: a meta-analysis of genetic risk.
European journal of obstetrics, gynecology, and reproductive biology 2015 Aug 191 106-11. Ziakas Panayiotis D, Poulou Loukia S, Pavlou Matthaios, Zintzaras Eli |
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Thrombophilic genetic factors PAI-1 4G-4G and MTHFR 677TT as risk factors of alcohol, cryptogenic liver cirrhosis and portal vein thrombosis, in a Caucasian population.
Gene 2015 Aug 568 (1): 85-8. D'Amico Mario, Pasta Francesca, Pasta Lin |
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A preliminary study of inherited thrombophilic risk factors in different clinical manifestations of venous thromboembolism in central Iran.
The Indian journal of medical research 2015 Jul 142 (1): 46-52. Karimi Ali, Abolhasani Marziyeh, Hashemzadeh-Chaleshtori Morteza, Pourgheysari Bato |
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The investigation of hereditary and acquired thrombophilia risk factors in the development of complications in pregnancy in Croatian women.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2015 Jul 1-6. Lenz Bahrija, Samardzija Marina, Drenjancevic Domagoj, Zibar Davor, Samardzija Marko, Milostic-Srb Andr |
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Association study of methylenetetrahydrofolate reductase C677T mutation with cerebral venous thrombosis in an Iranian population.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Jun . Ghaznavi Habib, Soheili Zahra, Samiei Shahram, Soltanpour Mohammad |
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Factor V Leiden, factor V Cambridge, factor II GA20210, and methylenetetrahydrofolate reductase in cerebral venous and sinus thrombosis: A case-control study.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2015 Jun 20 (6): 554-562. Saadatnia Mohammad, Salehi Mansour, Movahedian Ahmad, Shariat Seyed Ziaeddin Samsam, Salari Mehri, Tajmirriahi Marzieh, Asadimobarakeh Elham, Salehi Rasoul, Amini Gilda, Ebrahimi Homa, Kheradmand Ehs |
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Homocysteine, methylenetetrahydrofolate reductase, folate status and atherothrombosis: A mechanistic and clinical perspective.
Vascular pharmacology 2015 Jun . Santilli Francesca, Davì Giovanni, Patrono Car |
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Polymorphisms in prothrombotic genes in young stroke patients in Greece: a case-controlled study.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Jun 26 (4): 430-5. Ranellou Kyriaki, Paraskeva Anteia, Kyriazopoulos Panagiotis, Batistatou Anna, Evangelou Aggelos, El-Aly Mahmoud, Zis Panagiotis, Tavernarakis Antonios, Charalabopoulos Konstantin |
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Thrombophilic mutations as risk factor for retinal vein occlusion: a case-control study.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2015 May 21 (4): 373-7. Russo Patrizia Dello, Damante Giuseppe, Pasca Samantha, Turello Marina, Barillari Giovan |
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Impact of thrombophilic genes mutations on thrombosis risk in Egyptian nonmetastatic cancer patients.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2015 Apr 26 (3): 309-15. Wahba Mona Ahmed, Ismail Mona Ahmed, Saad Abeer Attia, Habashy Deena Mohamed, Hafeez Zeinab Mohamed Abdel, Boshnak Noha Husse |
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Venous Thromboembolism after Allogeneic Pediatric Hematopoietic Stem Cell Transplantation: A Single-Center Study.
Turkish journal of haematology : official journal of Turkish Society of Haematology 2015 Apr . Az?k Fatih, Gökçebay Dilek Gürlek, Tavil Betül, Pamir I??k, Tunç Bahattin, Uçkan Duy |
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Evaluation of cerebral venous thrombosis secondary to oral contraceptive use in adolescents.
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Jan 36 (1): 149-53. Özdemir Hasan H, Varol Sefer, Ak?l E?ref, Acar Abdullah, Demir Caner |
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Elevated risk of thrombophilia in agenesis of the vena cava as a factor for deep vein thrombosis.
Orphanet journal of rare diseases 2015 10 (1): 3. Sagban Tolga Atilla, Scharf Rüdiger E, Wagenhäuser Markus U, Oberhuber Alexander, Schelzig Hubert, Grabitz Klaus, Duran Mans |
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Evaluation of a high throughput method for the detection of mutations associated with thrombosis and hereditary hemochromatosis in brazilian blood donors.
PloS one 2015 10 (5): e0125460. Dionisio Tavares Niewiadonski Vivian, Dos Santos Bianchi Juliana Vieira, de Almeida-Neto Cesar, Gaburo Nelson, Sabino Ester Cerdei |
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Genetic risk factors in patients with deep venous thrombosis, a retrospective case control study on Iranian population.
Thrombosis journal 2015 13 35. Hosseini Soudabeh, Kalantar Ebrahim, Hosseini Maryam Sadat, Tabibian Shadi, Shamsizadeh Morteza, Dorgalaleh Akb |
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High Incidence of ACE/PAI-1 in Association to a Spectrum of Other Polymorphic Cardiovascular Genes Involving PBMCs Proinflammatory Cytokines in Hypertensive Hypercholesterolemic Patients: Reversibility with a Combination of ACE Inhibitor and Statin.
PloS one 2015 10 (5): e0127266. AlBacha Jeanne d'Arc, Khoury Mira, Mouawad Charbel, Haddad Katia, Hamoui Samar, Azar Albert, Fajloun Ziad, Makdissy Nehm |
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Impact of Inherited Prothrombotic Disorders on the Long-Term Clinical Outcome of Percutaneous Transluminal Angioplasty in Patients with Diabetes.
Journal of diabetes research 2015 2015 369758. Dubský Michal, Jirkovská Alexandra, Pagá?ová Libuše, Bém Robert, N?mcová Andrea, Fejfarová Vladimíra, Wosková Veronika, Jude Edward |
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Pulmonary Embolism in a Sarcoidosis Patient Double Heterozygous for Methylenetetrahydrofolate Reductase Gene Polymorphisms and Factor V Leiden and Homozygous for the D-Allele of Angiotensin Converting Enzyme Gene.
Case reports in medicine 2015 2015 606805. El-Majzoub Nadim, Mahfouz Rami, Kanj Nad |
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Thrombophilic polymorphisms are not associated with disease-free survival in breast cancer patients.
International journal of clinical and experimental medicine 2015 8 (5): 8115-21. Ero?lu Aydan, Y?lmaz Ayfer Ezgi, Karasoy Dur |
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Clinical Implications of Methylenetetrahydrofolate Reductase Mutations and Plasma Homocysteine Levels in Patients with Thromboembolic Occlusion.
Vascular specialist international 2014 Dec 30 (4): 113-9. Park Won-Cheol, Chang Jeong-Hw |
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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 : the official journal of the Japan Society of Hepatology 2014 Dec 44 (14): E480-98. Qi Xingshun, Yang Zhiping, De Stefano Valerio, Fan Daimi |
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Prevalence of genetic prothrombotic risk factors: 1691G > A FV, 20210G > A PT and 677C > T MTHFR mutations in the Bosnian population.
Annals of human biology 2014 Oct 1-5. Adler Gra?yna, Agnieszka Garstka, Valjevac Amina, Czerska Ewa, Kiseljakovic Emina, Salkic Nermin Nusr |
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Plasma homocysteine concentrations in acute and convalescent changes of central retinal vein occlusion in a Chinese population.
Investigative ophthalmology & visual science 2014 Jul 55 (7): 4057-62. Dong Ning, Xu Bing, Tang X |
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Adaptive developmental plasticity in methylene tetrahydrofolate reductase (MTHFR) C677T polymorphism limits its frequency in South Indians.
Molecular biology reports 2014 May 41 (5): 3045-50. Naushad Shaik Mohammad, Krishnaprasad Chintakindi, Devi Akella Radha Ra |
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Association of methylenetetrahydrofolate reductase (A1298C and C677T) polymorphisms with retinal vein occlusion in Tunisian patients.
Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis 2014 Apr 50 (2): 283-7. Mrad Meriem, Wathek Cheima, Saleh Mekki Ben, Baatour Makrem, Rannen Riadh, Lamine Khaled, Gabsi Salem, Gritli Nasreddine, Fekih-Mrissa Naji |
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Combined genetic mutations have remarkable effect on deep venous thrombosis and/or pulmonary embolism occurence.
Gene 2014 Feb 536 (1): 171-6. Simsek Erdal, Yesilyurt Ahmet, Pinarli Ferda, Eyerci Nilnur, Ulus A Tul |
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Impact of inherited thrombophilia on the risk of recurrent venous thromboembolism onset in Georgian population.
Georgian medical news 2014 Feb (227): 93-7. Pirtskhelani N, Kochiashvili N, Makhaldiani L, Pargalava N, Gaprindashvili E, Kartvelishvili |
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The relationship between factor V Leiden, prothrombin G20210A, and MTHFR mutations and the first major thrombotic episode in polycythemia vera and essential thrombocythemia.
Annals of hematology 2014 Feb 93 (2): 203-9. Trifa Adrian P, Cucuianu Andrei, Popp Radu A, Coad? Camelia A, Costache Roxana M, Militaru Mariela S, Vesa ?tefan C, Pop Ioan |
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The role of point mutations in the genes, predisposing inherited thrombophilia in the pathogeneses of proximal and distal deep vein thrombosis in Georgian population.
Georgian medical news 2014 Feb (227): 98-102. Pirtskhelani N, Kochiashvili N, Makhaldiani L, Pargalava N, Gaprindashvili E, Kartvelishvili |
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Hyperhomocysteinemia and methylenetetrahydrofolate reductase C677T polymorphism in cerebral veno-sinus thrombosis.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2014 Jan 20 (1): 78-83. Bharatkumar Venkata Pinnelli, Nagaraja Dindagur, Christopher Ri |
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[Prognostic value of allelic variants affecting the hemostatic system in the development of antiphospholipid syndrome and kidney lesion in patients with systemic lupus erythematosus].
Terapevticheski? arkhiv 2014 86 (6): 57-62. Borisov E N, Krasnova T N, Samohodskaia L M, Ivanitski? L V, Nikiforova N V, Mukhin N |
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Homocysteine, methylenetetrahydrofolate reductase C677T polymorphism, and risk of retinal vein occlusion: an updated meta-analysis.
BMC ophthalmology 2014 14 147. Li Dan, Zhou Minwen, Peng Xiaoyan, Sun Hui |
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PAI-1 4G/5G and MTHFR C677T polymorphisms increased the accuracy of two prediction scores for the risk of acute lower extremity deep vein thrombosis.
Romanian journal of morphology and embryology = Revue roumaine de morphologie et embryologie 2014 55 (1): 153-7. Pop Tudor Radu, Vesa ?tefan Cristian, Trifa Adrian Pavel, Cri?an Sorin, Buzoianu Anca Da |
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Thrombophilia in patients with retinal vein occlusion: a retrospective analysis.
Ophthalmologica. Journal international d'ophtalmologie. International journal of ophthalmology. Zeitschrift für Augenheilkunde 2014 232 (1): 46-52. Risse Franziska, Frank Rolf Dario, Weinberger Andreas W |
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Significance of the use of the ViennaLab "Cardiovascular Disease panel" (CVD) Assay as a reflex test for the "Factor V/II/MTHFR Assay".
Meta gene 2013 Dec 1 76-81. Hoteit Rouba, Abbas Fatmeh, Antar Ahmad, Abdel Khalek Rabab, Shammaa Dina, Mahfouz Ra |
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Association between polymorphism of MTHFR c.677C>T and risk of cardiovascular disease in Turkish population: a meta-analysis for 2.780 cases and 3.022 controls.
Molecular biology reports 2013 Nov . Bozok Çetinta? V, Gündüz C |
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Plasma homocysteine concentrations in the acute phase after central retinal vein occlusion in a Chinese population.
Current eye research 2013 Nov 38 (11): 1153-8. Dong Ning, Wang Bingsong, Chu Liqun, Xiao L |
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Who are at risk for thromboembolism after arthroplasty? A systematic review and meta-analysis.
Thrombosis research 2013 Nov 132 (5): 531-6. Zhou Xindie, Qian Wenkang, Li Jin, Zhang Pengli, Yang Zhigao, Chen Weiping, Wu Lido |
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Clinical significance of determining plasma homocysteine: case-control study on arterial and venous thrombotic patients.
Croatian medical journal 2013 Oct 54 (5): 480-8. Vuckovic Biljana A, Cabarkapa Velibor S, Ilic Tatjana A, Salatic Iva R, Lozanov-Crvenkovic Zagorka S, Mitic Gorana |
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Hyperhomocysteinemia in patients with Crohn's disease.
Techniques in coloproctology 2013 Oct 17 (5): 497-500. Casella G, Antonelli E, Di Bella C, Di Marco E, Piatti M, Villanacci V, Bologna S, Baldini V, Bassotti |
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Prevalence of MTHFR C677T single nucleotide polymorphism in genetically isolated populations in Jordan.
Biochemical genetics 2013 Oct 51 (9-10): 780-8. Dajani Rana, Fathallah Raja, Arafat Ala, AbdulQader Mohammed Emad, Hakooz Nancy, Al-Motassem Yousef, El-Khateeb Mohamm |
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Clinical impact of Factor V Leiden, Prothrombin G20210A and MTHFR C677T mutations among sickle cell disease patients of Central India.
European journal of haematology 2013 Sep . Nishank SS, Singh M, Yadav R |
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Effect of thrombosis-related gene polymorphisms upon oral cancer: a regression analysis.
Anticancer research 2013 Sep 33 (9): 4033-9. Vylliotis Antonis, Yapijakis Christos, Nkenke Emeka, Nisyrios Themistoklis, Avgoustidis Dimitrios, Adamopoulou Maria, Ragos Vasilios, Vassiliou Stavros, Koronellos Nikolas, Vairaktaris Eleftheri |
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Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis involving over 11,000 cases and 21,000 controls.
European journal of epidemiology 2013 Aug 28 (8): 621-47. Simone Benedetto, De Stefano Valerio, Leoncini Emanuele, Zacho Jeppe, Martinelli Ida, Emmerich Joseph, Rossi Elena, Folsom Aaron R, Almawi Wassim Y, Scarabin Pierre Y, den Heijer Martin, Cushman Mary, Penco Silvana, Vaya Amparo, Angchaisuksiri Pantep, Okumus Gulfer, Gemmati Donato, Cima Simona, Akar Nejat, Oguzulgen Kivilcim I, Ducros Véronique, Lichy Christoph, Fernandez-Miranda Consuelo, Szczeklik Andrzej, Nieto José A, Torres Jose Domingo, Le Cam-Duchez Véronique, Ivanov Petar, Cantu-Brito Carlos, Shmeleva Veronika M, Stegnar Mojka, Ogunyemi Dotun, Eid Suhair S, Nicolotti Nicola, De Feo Emma, Ricciardi Walter, Boccia Stefan |
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The methylenetetrahydrofolate reductase polymorphism (MTHFR c.677C>T) and elevated plasma homocysteine levels in a U.S. pediatric population with incident thromboembolism.
Thrombosis research 2013 Aug 132 (2): 170-4. Joachim Emily, Goldenberg Neil A, Bernard Timothy J, Armstrong-Wells Jennifer, Stabler Sally, Manco-Johnson Marilyn |
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Factors associated with the development of superficial vein thrombosis in patients with varicose veins.
Thrombosis research 2013 Jul 132 (1): 47-50. Karathanos Christos, Exarchou Maria, Tsezou Aspasia, Kyriakou Despina, Wittens Cees, Giannoukas Athanasi |
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Assessment of genetic risk factors for thromboembolic complications in adults with idiopathic nephrotic syndrome.
Clinical nephrology 2013 Jun 79 (6): 454-62. Sahin Melisa, Ozkurt Sultan, Degirmenci Nevbahar Akcar, Musmul Ahmet, Temiz Gokhan, Soydan Mehm |
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Methylenetetrahydrofolate reductase C677T mutation and risk of retinal vein thrombosis.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2013 Jun 18 (6): 487-91. Soltanpour Mohammad Soleiman, Soheili Zahra, Shakerizadeh Ali, Pourfathollah Ali Akbar, Samiei Shahram, Meshkani Reza, Shahjahani Mohammad, Karimi Abb |
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