HuGE Literature Finder
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| Identification of genetic risk factors associated with ischaemic stroke in young Mexican patients. Neurologia (Barcelona, Spain) 2021 Jun 36 (5): 337-345. 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 |
| Prevalence of thrombophilia-associated genetic risk factors in blood donors of a regional hospital in southern Brazil. Hematology, transfusion and cell therapy 2021 Mar . Dick-Guareschi Jéssica, Fontana Juliana Cristine, Sanseverino Maria Teresa Vieira, Kubaski Francyne, Sekine Leo, Mesquita Nanci Félix, Onsten Tor Gunnar Hugo, Leistner-Segal Sand |
| Inherited and acquired thrombophilia in adults with retinal vascular occlusion: A systematic review and meta-analysis. Journal of thrombosis and haemostasis : JTH 2020 Aug . Romiti Giulio Francesco, Corica Bernadette, Borgi Marco, Visioli Giacomo, Pacella Elena, Cangemi Roberto, Proietti Marco, Basili Stefania, Raparelli Valer |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| Prevalence of F5 1691G>A, F2 20210G>A, and MTHFR 677C>T 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 |
| 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 |
| 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 |
| Interactions among methylenetetrahydrofolate reductase (MTHFR) and cystathionine ß-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 |
| 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 |
| 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 |
| Association of Mycobacterium infections in patients with Mendelian susceptibility to mycobacterial disease 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 |
| 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, |
| 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 |
| 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 |
| 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 |
| 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 |
| Incidence of the MTHFR polymorphisms in patients with varicose veins. Hippokratia 0 21 (4): 175-179. Ekim M, Ekim |
| Methylenetetrahydrofolate reductase polymorphism in healthy volunteers and its correlation with homocysteine levels in patients with thrombosis. Indian journal of pharmacology 0 51 (4): 248-254. Munshi Renuka, Panchal Falguni, Kulkarni Vrinda, Chaurasia Aj |
- Page last reviewed:Oct 1, 2021
- Page last updated:May 18, 2022
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