Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 131 Records) |
| Query Trace: Venous Thrombosis and MTHFR[original query] |
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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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| A Patient with Ulcerative Colitis Complicated by Systemic Vein Thrombosis. Case reports in gastroenterology 2018 7 12 (2): 322-326. Meštrovi? Antonio, Žaja Ivan, Ardali? Žarko, Vrebalov-Cindro Pavle, Šusti? Ivan, Puljiz Marko, Bratani? Andre, Bonacin Dam |
| Prevalence of factor V leiden, MTHFR C677T and MTHFR A1298C polymorphisms in patients with deep vein thrombosis in Central Iran. Molecular biology reports 2018 6 45 (4): 621-624. Ehsani Majid, Imani Aida, Moravveji Alire |
| 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 |
| 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 |
| 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 |
| Genetic risk factors for venous thromboembolism among infertile men with Klinefelter syndrome. Journal of clinical & translational endocrinology 2020 6 20 100228. Hussein Tarek M, Abd Elmoaty Elneily Dalia, Mohamed Abdelfattah Elsayed Fatma, El-Attar Lama |
| Inherited Thrombophilia in a Lebanese Family of Four Generations: A Case Report of Recurrent Miscarriage. Vascular health and risk management 2020 2 16 53-56. Khalife Sara, Bissar-Tadmouri Nisri |
| Association of Genetic Variants with Hyperhomocysteinemia in Indian Patients with Thrombosis. Indian journal of clinical biochemistry : IJCB 2020 10 35 (4): 465-473. Paradkar Minal Umesh, Padate Balkrishna, Shah Swarup A V, Vora Hiral, Ashavaid Tester |
| Prevalence and Multiplicity of Thrombophilia Genetic Polymorphisms of F V, MTHFR, F II, and PAI -I: A Cross-Sectional Study on a Healthy Jordanian Population. International journal of general medicine 2021 14 5323-5332. Al-Zoubi Nabil, Alrabadi Nasr, Kheirallah Khalid, Alqudah Ahm |
| Targeted next-generation sequencing reveals novel and known variants of thrombophilia associated genes in Saudi patients with venous thromboembolism. Clinica chimica acta; international journal of clinical chemistry 2021 5 519 247-254. Athar Mohammad, Ghita Ibrahim S, Albagenny Amani A, Abduljaleel Zainularifeen, Shadab Ghulam, Elsendiony Ahmed, Halawani Saeed H, Alkazmi Mohammad M, Alquthami Khalid, Alkhuzae Mohammad M, Althebyani Abdulaziz A, Bogari Neda M, Dannoun Anas, Al-Allaf Faisal |
| 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 |
| Comprehensive Thrombophilia Evaluation in Cerebral Venous Thrombosis: A Single Center Cross Sectional Study. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2022 6 38 (3): 522-528. Kumar Rajiv, Vinny Pulikottil Wilson, Nair Vishnu G, Jakku Raje |
| A call to action: MTHFR polymorphisms should not be a part of inherited thrombophilia testing. Research and practice in thrombosis and haemostasis 2022 6 6 (4): e12739. Deloughery Thomas G, Hunt Beverley J, Barnes Geoffrey D, Connors Jean M, |
| Thromboembolism in Children. Indian journal of pediatrics 2023 5 . Yurday Öncül, Arzu Akyay, Ünsal Özg |
| Ischaemic stroke with multi-focal venous and arterial thrombosis due to hyperhomocysteinemia: anabolic androgenic steroid use and MTHFR c.667 C?>?T variant - a case report. BMC neurology 2023 4 23 (1): 167. Jpk Chen, A Rees, C H Coughlan, W Goodison, E Murphy, A Chandrathe |
| [Hereditary Spherocytosis and Pregnancy: A Case Report]. Acta medica portuguesa 2023 2 . Miguel Andreia, Alves Maria José, Massa Ana Catari |
- Page last reviewed:Feb 1, 2023
- Page last updated:Jun 02, 2023
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