HuGE Literature Finder
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Records 1-100
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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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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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Thrombophilia in Klinefelter Syndrome With Deep Venous Thrombosis, Pulmonary Embolism, and Mesenteric Artery Thrombosis on Testosterone Therapy: A Pilot Study.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2016 Aug . Glueck Charles J, Jetty Vybhav, Goldenberg Naila, Shah Parth, Wang Pi |
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Impact of Prothrombotic Risk Factors in a Cohort of Egyptian Hemophilia A Patients.
Molecular diagnosis & therapy 2016 Feb . Hamdy Mona Salah El-Din, Nasr Aml Soliman, Makhlouf Manal Mohamed, El-Saadany Zainab Ali, Samir Magy, Morgan Dalia Sab |
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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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Risk factors associated with inhibitor development in Chinese patients with haemophilia B.
Haemophilia : the official journal of the World Federation of Hemophilia 2015 Jul 21 (4): e286-93. Zhou J, Ding Q, Chen Z, Yang H, Lin L, Wang H, Wang X, Wu |
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[Congenital hypofibrinogenemia associated with a novel mutation in FGG gene].
Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2015 Jun 32 (3): 331-4. Wang Yingyu, Ding Hongxiang, Hao Xiuping, Zhu Liqing, Yang Lihong, Jin Yanhui, Wang Mingsh |
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Influence of factor 5 rs6025 and factor 2 rs1799963 mutation on inhibitor development in patients with hemophilia A--an Israeli-German multicenter database study.
Thrombosis research 2014 Apr 133 (4): 544-9. Kenet Gili, Bidlingmaier Christoph, Bogdanova Nadja, Ettingshausen Carmen Escuriola, Goldenberg Neil, Gutsche Sven, Halimeh Susan, Holzhauer Susanne, Kurnik Karin, Limperger Verena, Junker Ralf, Nowak-Göttl Ulri |
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Risk factors and recurrent thrombotic episodes in patients with cerebral venous thrombosis.
Blood transfusion = Trasfusione del sangue 2014 Jan 12 Suppl 1 s337-42. Tufano Antonella, Guida Anna, Coppola Antonio, Nardo Assunta, Di Capua Mirko, Quintavalle Gabriele, Di Minno Matteo Nicola Dario, Cerbone Anna Maria, Di Minno Giovan |
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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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The role of the factor V Leiden mutation in osteonecrosis of the hip.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2013 Sep 19 (5): 499-503. Glueck Charles J, Freiberg Richard A, Boriel Gail, Khan Zia, Brar Amanpreet, Padda Jagjit, Wang Pi |
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Prediction of ischemic stroke in young Indians: is thrombophilia profiling a way out?
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Jun 24 (4): 449-53. Chatterjee Tathagata, Gupta Neha, Choudhry Ved Prakash, Behari Madhuri, Saxena Renu, Ashraf Mohammad |
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Thrombotic risk factors in Chinese Budd-Chiari syndrome patients. An observational study with a systematic review of the literature.
Thrombosis and haemostasis 2013 May 109 (5): 878-84. Qi X, Wu F, Ren W, He C, Yin Z, Niu J, Bai M, Yang Z, Wu K, Fan D, Han |
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Maternal cerebral venous thrombosis, uncommon but serious disorder, pathologic predictors and contribution of prothrombotic abnormalities.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Apr 24 (3): 269-72. Klai Sarra, Fekih-Mrissa Najiba, Mrissa Ridha, Rachdi Radhouen, Gritli Nasredi |
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Thrombophilia in Patients With Lower Limbs Deep Veins Thrombosis (LDVT) Results of a Monocentric Survey on 103 Consecutive Outpatients.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2013 Jan . Signorelli SS, Fiore V, Puccia G, Mastrosimone G, Anzaldi M |
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[Evaluation of coagulopathies and fibrinolytic abnormalities in central retinal vein occlusion in patients under 60years of age.]
Journal francais d'ophtalmologie 2012 Dec . Tea S, Barrali M, Racadot E, Delbosc B |
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Evaluation of the presence of hereditary and acquired thrombophilias in Brazilian children and adolescents with diagnoses of portal vein thrombosis.
Journal of pediatric gastroenterology and nutrition 2012 Nov 55 (5): 599-604. Ferri Priscila Menezes, Rodrigues Ferreira Alexandre, Fagundes Eleonora Druve Tavares, Xavier Sandra Guerra, Dias Ribeiro Daniel, Fernandes Ana Paula, Borges Karina Braga Gomes, Liu Shinfay Maximilian, de Melo Maria do Carmo Barros, Roquete Mariza Leitão Valadares, Penna Francisco Jo |
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Sample-to-SNP kit: a reliable, easy and fast tool for the detection of HFE p.H63D and p.C282Y variations associated to hereditary hemochromatosis.
Gene 2012 Oct 507 (1): 79-84. Nielsen Peter B, Petersen Maja S, Ystaas Viviana, Andersen Rolf V, Hansen Karin M, Blaabjerg Vibeke, Refstrup Met |
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The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia.
Journal of thrombosis and thrombolysis 2012 Oct 34 (3): 406-9. Bôžiková Alexandra, Gabriková Dana, Sovi?ová Adriana, Behulová Regina, Ma?eková So?a, Boro?ová Iveta, Petrej?íková Eva, Soták Miroslav, Bernasovská Jarmila, Bernasovský Iv |
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MTHFR polymorphic variant C677T is associated to vascular complications in sickle-cell disease.
Genetic testing and molecular biomarkers 2012 Sep 16 (9): 1038-43. Hatzlhofer Betânia L D, Bezerra Marcos André C, Santos Magnun N N, Albuquerque Dulcinéia M, Freitas Elizabete M, Costa Fernando F, Araújo Aderson S, Muniz Maria Tereza |
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Prevalence of coagulation factor II G20210A and factor V G1691A Leiden polymorphisms in Chechans, a genetically isolated population in Jordan.
Molecular biology reports 2012 Sep 39 (9): 9133-8. Dajani Rana, Fatahallah Raja, Dajani Abdelrahman, Al-Shboul Mohammad, Khader Yous |
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Factor V Leiden, prothrombin 20210G>A, MTHFR 677C>T and 1298A>C, and homocysteinemia in Tunisian blood donors.
Journal of clinical laboratory analysis 2012 May 26 (3): 167-73. Hadhri Samira, Rejab Mohamed Ben, Guedria Hajer, Ifa Lamia, Chatti Noureddine, Skouri Had |
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The thrombophilic pattern of different clinical manifestations of venous thromboembolism: a survey of 443 cases of venous thromboembolism.
Seminars in thrombosis and hemostasis 2012 Mar 38 (2): 230-4. Grifoni Elisa, Marcucci Rossella, Ciuti Gabriele, Cenci Caterina, Poli Daniela, Mannini Lucia, Liotta Agatina Alessandrello, Miniati Massimo, Abbate Rosanna, Prisco Domeni |
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Subclinical central nervous system involvement and thrombophilic status in young thalassemia intermedia patients of Greek origin.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2012 Feb . Teli A, Economou M, Rudolf J, Tzovaras F, Gourtsa V, Kondou A, Kontopoulos E, Gombakis N, Athanassiou-Metaxa M, Zafeiriou D |
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Thrombophilia among Chinese women with venous thromboembolism during pregnancy.
Gynecologic and obstetric investigation 2012 73 (3): 183-8. Tam Wing-Hung, Ng Margaret Heung-Ling, Yiu Alice Ka-Wah, Lau Kin-Mang, Cheng Gregory Yin-Ming, Li Chi-Y |
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The association of inherited thrombophilia and intrauterine fetal death: a case-control study.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2011 Dec 22 (8): 8. Helgadottir LB, Skjeldestad FE, Jacobsen AF, Sandset PM, Jacobsen EM |
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Hereditary thrombophilia in an unselected cohort of venous thrombosis patients in Singapore.
Journal of clinical pathology 2011 Sep 64 (9): 814-7. Lee Lai Heng, Liu Te Chih, Kuperan Ponnudurai, Tan Lip Kun, Tan Daryl, Poon Michelle L, Ong Kiat Hoe, Fong Sing Zern, Tan Melissa Y, Ng Heng J |
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Genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro, Brazil.
Arquivos de neuro-psiquiatria 2011 Jun 69 (3): 431-5. Filho Isaac Lima da Silva, Leite Ana Claudia Celestino Bezerra, Moura Patrícia Gomes, Ribeiro Georgina Severo, Cavalcante Andréa Cony, Azevedo Flávia Carolina Marques de, Andrada-Serpa Maria José |
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THROMBOPHILIC SCREENING IN TURNER SYNDROME.
Journal of endocrinological investigation 2011 May . Calcaterra V, Gamba G, Montani N, de Silvestri A, Terulla V, Lanati G, Larizza D |
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Acquired activated protein C resistance, thrombophilia and adverse pregnancy outcomes: a study performed in an Irish cohort of pregnant women.
Journal of pregnancy 2011 2011 232840. Sedano-Balbás Sara, Lyons Mark, Cleary Brendan, Murray Margaret, Gaffney Geraldine, Maher Majel |
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The status of thrombophilic defects and non-O blood group as risk factors for gestational vascular complications among Tunisian women.
Acta haematologica 2011 125 (3): 115-20. Klai Sarra, Fekih-Mrissa Najiba, Rachdi Radhouen, Gritli Nasredi |
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Impact of thrombogenic mutations on clinical phenotypes of von Willebrand disease.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2010 Jun 16 (3): 281-7. Ahmad Firdos, Kannan Meganathan, Yadav Vinita, Biswas Arijit, Saxena Re |
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Vascular at-risk genotypes and disease severity in Lebanese sickle cell disease patients.
American journal of hematology 2010 May 85 (5): 395-6. Farra Chantal, Zahed Laila, Nietert Paul J, Hourani Hala, Jradi Oussama, Inati Adlette, Mahfouz Rami, Abboud Miguel, Oberkanins Christi |
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Role of thrombotic risk factors in end-stage renal disease.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2010 Apr 16 (2): 132-40. Tripathi Gaurav, Sankhwar Satya Narayan, Sharma Raj Kumar, Baburaj Vinod Pandirikkal, Agrawal Suraks |
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Risk factors for clinical manifestations in carriers of Factor V Leiden and prothrombin gene mutations.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2010 Jan 21 (1): 11-5. DeSancho Maria Teresa, Berlus Nickisha, Christos Paul J, Rand Jac |
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The impact of prothrombotic mutations on factor consumption in adult patients with severe hemophilia.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009 Dec 15 (6): 660-5. Ar M Cem, Baykara Onur, Buyru Ayse Nur, Baslar Zaf |
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The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with beta-thalassemia major.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009 Dec 20 (8): 675-8. Al-Sweedan Suleimman A, Jaradat Said, Iraqi Muna, Beshtawi Moham |
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The prevalence of factor V Leiden, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T among G6PD deficient individuals from Western Iran.
Molecular biology reports 2009 Nov 36 (8): 2361-4. Mozafari Hadi, Rahimi Zohreh, Heidarpour Azadeh, Fallahi Mahsa, Muniz Adraia |
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Congenital thrombotic risk factors in beta-thalassemia.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2009 Oct 15 (5): 581-4. Sipahi Tansu, Kara Aslihan, Kuybulu Ayca, Egin Yonca, Akar Nej |
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Thrombin generation and D-dimer concentrations in a patient cohort investigated for venous thromboembolism. Relations to venous thrombosis, factor V Leiden and prothrombin G20210A. The LIST study.
Thrombosis research 2009 Jun 124 (2): 178-84. Chaireti Roza, Jennersjö Cecilia, Lindahl Tomas |
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Modulation of clinical phenotype of Glanzmann's thrombasthenia by thrombogenic mutations.
Clinica chimica acta; international journal of clinical chemistry 2009 May 403 (1-2): 156-8. Kannan Meganathan, Yadav Birendra Kumar, Ahmad Firdos, Biswas Arijit, Saxena Re |
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Association of inherited thrombophilia with embryonic and postembryonic recurrent pregnancy loss.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2009 Mar 20 (2): 134-40. Ivanov Petar D, Komsa-Penkova Regina S, Konova Emiliana I, Kovacheva Katia S, Simeonova Maria N, Popov Jordan |
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Usefulness of genetic polymorphisms and conventional risk factors to predict coronary heart disease in patients with familial hypercholesterolemia.
The American journal of cardiology 2009 Feb 103 (3): 375-80. van der Net Jeroen B, Janssens A Cecile J W, Defesche Joep C, Kastelein John J P, Sijbrands Eric J G, Steyerberg Ewout |
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Prevalence of thrombotic risk factors among beta-thalassemia patients from Western Iran.
Journal of thrombosis and thrombolysis 2008 Dec 26 (3): 229-33. Rahimi Zohreh, Ghaderi Mandana, Nagel Ronald L, Muniz Adria |
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The prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian antenatal population.
The Australian & New Zealand journal of obstetrics & gynaecology 2008 Dec 48 (6): 536-41. Said Joanne M, Brennecke Shaun P, Moses Eric K, Walker Susan P, Monagle Paul T, Campbell Janine, Bryant Valerie J, Borg Anthony J, Higgins John |
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Perthes' disease and the search for genetic associations: collagen mutations, Gaucher's disease and thrombophilia.
The Journal of bone and joint surgery. British volume 2008 Nov 90 (11): 1507-11. Kenet G, Ezra E, Wientroub S, Steinberg D M, Rosenberg N, Waldman D, Hayek |
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Factor V Leiden, prothrombin G20210A, and protein C mutation frequency in Turkish venous thrombosis patients.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2008 Oct 14 (4): 415-20. Altinisik Julide, Ates Omer, Ulutin Turgut, Cengiz Mujgan, Buyru N |
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Nonstroke arterial thrombosis in children: Hacettepe experience.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008 Sep 19 (6): 519-24. Balci Yasemin Isik, Unal Sule, Gumruk Fatma, Cetin Mualla, Ozkutlu Suheyla, Gurgey Aytem |
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The risk of symptomatic pulmonary embolism due to proximal deep venous thrombosis differs in patients with different types of inherited thrombophilia.
Thrombosis and haemostasis 2008 Jun 99 (6): 1030-4. Rossi E, Za T, Ciminello A, Leone G, De Stefano V |
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Thrombophilic mutations among Southern Iranian patients with sickle cell disease: high prevalence of factor V Leiden.
Journal of thrombosis and thrombolysis 2008 Jun 25 (3): 288-92. Rahimi Zohreh, Vaisi-Raygani Asad, Nagel Ronald L, Muniz Adria |
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Thrombosis in children with cardiac pathology: analysis of acquired and inherited risk factors.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2008 Jun 19 (4): 294-304. Alioglu Bulent, Avci Zekai, Tokel Kursat, Atac F Belgin, Ozbek Nam |
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Inheritance and perinatal consequences of inherited thrombophilia in Greece.
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics 2008 Feb 100 (2): 124-9. Karakantza Marina, Androutsopoulos Georgios, Mougiou Athina, Sakellaropoulos Georgios, Kourounis Georgios, Decavalas Georgi |
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The role of thrombophilia and thyroid autoimmunity in unexplained infertility, implantation failure and recurrent spontaneous abortion.
Human reproduction (Oxford, England) 2008 Feb 23 (2): 278-84. Bellver José, Soares Sergio R, Alvarez Claudio, Muñoz Elkin, Ramírez Alberto, Rubio Carmen, Serra Vicente, Remohí José, Pellicer Anton |
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Thrombophilia differences in cerebral venous sinus and lower extremity deep venous thrombosis.
Neurology 2008 Feb 70 (8): 627-33. Wysokinska E M, Wysokinski W E, Brown R D, Karnicki K, Gosk-Beirska I, Grill D, McBane R |
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Maternal factor V Leiden mutation is associated with HELLP syndrome in Caucasian women.
Acta obstetricia et gynecologica Scandinavica 2008 87 (6): 635-42. Muetze Sabine, Leeners Brigitte, Ortlepp Jan R, Kuse Sabine, Tag Carmen G, Weiskirchen Ralf, Gressner Axel M, Rudnik-Schoeneborn Sabine, Zerres Klaus, Rath Wern |
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Risk factors of venous thromboembolism in thai patients.
International journal of hematology 2007 Dec 86 (5): 397-402. Angchaisuksiri Pantep, Atichartakarn Vichai, Aryurachai Katcharin, Archararit Napaporn, Rachakom Buppa, Atamasirikul Kanlayanee, Tiraganjana Arj |
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CYP2C9 and VKORC1 genetic polymorphism analysis might be necessary in patients with Factor V Leiden and prothrombin gene G2021A mutation(s).
Diagnostic molecular pathology : the American journal of surgical pathology, part B 2007 Sep 16 (3): 184-6. Leung Allen, Huang Chih-Kang, Muto Riho, Liu Yinxian, Pan Qiu |
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Frequency of selected thrombophilias in women with placental abruption.
The Australian & New Zealand journal of obstetrics & gynaecology 2007 Aug 47 (4): 297-301. Procházka Martin, Lubuský Marek, Slavík Ludek, Hrachovec Petr, Zielina Petr, Kudela Milan, Lindqvist Pelle |
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The risk of recurrent venous thromboembolism among heterozygous carriers of factor V Leiden or prothrombin G20210A mutation. A systematic review of prospective studies.
Haematologica 2007 Aug 92 (8): 1107-14. Marchiori Antonio, Mosena Laura, Prins Martin H, Prandoni Pao |
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Effects of the factor V G1691A mutation and the factor II G20210A variant on the clinical expression of severe hemophilia A in children--results of a multicenter studys.
Haematologica 2007 Jul 92 (7): 982-5. Kurnik Karin, Kreuz Wolfhart, Horneff Sylvia, Düring Christine, Schobess Rosemarie, Bidlingmaier Christoph, Ettingshausen Carmen Escuriola, Krümpel Anne, Bogdanova Nadia, Nowak-Göttl Ulri |
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Hyperhomocysteinemia and the compound heterozygous state for methylene tetrahydrofolate reductase are independent risk factors for deep vein thrombosis among South Indians.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2007 Mar 18 (2): 113-7. Naushad Sm, Jamal Nurul Jain, Angalena R, Prasad C Krishna, Devi A Radha Ra |
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[Hyperhomocysteinemia--one of the factors underlying thrombotic complications in patients with chronic myeloproliferative diseases].
Terapevticheski? arkhiv 2007 79 (12): 57-62. Sokolova M A, Khoroshko N D, Tsvetaeva N V, Turkina A G, Levina A A, Mamukova Iu I, Rokhnianskaia A A, Sudarikov A B, Romanova E A, Vasil'ev S A, Sukhanova G A, Orel E B, Rudakova V E, Tutaeva V V, Manakova T E, Semenova E A, Kulikov S |
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Congenital prothrombotic disorders in children with peripheral venous and arterial thromboses.
Acta haematologica 2007 117 (3): 149-55. Albisetti Manuela, Moeller Alexander, Waldvogel Katharina, Bernet-Buettiker Vera, Cannizzaro Vincenzo, Anagnostopoulos Alexia, Balmer Christian, Schmugge Mark |
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Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population.
American journal of hematology 2006 Dec 81 (12): 933-7. Torres J D, Cardona H, Alvarez L, Cardona-Maya W, Castañeda S A, Quintero-Rivera F, Cadavid A, Bedoya G, Tobón |
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Screening for inherited thrombophilia might be warranted among Eastern Mediterranean sickle-beta-0 thalassemia patients.
Journal of thrombosis and thrombolysis 2006 Oct 22 (2): 121-3. Isma'eel Hussain, Arnaout M S, Shamseddeen Wael, Mahfouz R, Zeineh N, Jradi Oussama, Taher A |
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The clinical impact of MTHFR polymorphism on the vascular complications of sickle cell disease.
Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2006 Oct 39 (10): 1291-5. Moreira Neto F, Lourenço D M, Noguti M A E, Morelli V M, Gil I C P, Beltrão A C S, Figueiredo M |
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Ethnic differences in the prevalence of inherited thrombophilic polymorphisms in an asymptomatic Australian prenatal population.
Human biology 2006 Aug 78 (4): 403-12. Said Joanne M, Brennecke Shaun P, Moses Eric K, Walker Susan P, Borg Anthony J, Williams Jeff T, Higgins John |
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Genetic polymorphisms of hemostasis genes and primary outcome of very low birth weight infants.
Pediatrics 2006 Aug 118 (2): 683-9. Härtel Christoph, König Inke, Köster Stefan, Kattner Evelyn, Kuhls Eckhardt, Küster Helmut, Möller Jens, Müller Dirk, Kribs Angela, Segerer Hugo, Wieg Christian, Herting Egbert, Göpel Wolfga |
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Frequency of thrombophilia-related genetic variations in patients with idiopathic pulmonary embolism in an urban emergency department.
Clinical chemistry 2006 Jun 52 (6): 1026-32. Kruse Lori, Mitchell Alice M, Camargo Carlos A, Hernandez Jackeline, Kline Jeffrey |
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High prevalence of inherited prothrombotic risk factors in 134 consecutive patients with von Willebrand disease.
American journal of hematology 2006 Jun 81 (6): 465-7. Franchini Massimo, Veneri Dino, Poli Giovanni, Manzato Franco, Salvagno Gian Luca, Lippi Giusep |
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Thrombophilic risk factors and homocysteine levels in Behçet's disease in eastern Spain and their association with thrombotic events.
Thrombosis and haemostasis 2006 Apr 95 (4): 618-24. Ricart José Ma, Vayá Amparo, Todolí José, Calvo Javier, Villa Piedad, Estellés Amparo, España Francisco, Santaolaria Marisa, Corella Dolores, Aznar Jus |
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Genetic determinants of cardiovascular disease risk in familial hypercholesterolemia.
Arteriosclerosis, thrombosis, and vascular biology 2005 Jul 25 (7): 1475-81. Jansen Angelique C M, van Aalst-Cohen Emily S, Tanck Michael W T, Cheng Suzanne, Fontecha Marcel R, Li Jia, Defesche Joep C, Kastelein John J |
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Prevalence of hyperhomocysteinaemia, activated protein C resistance and prothrombin gene mutation in inflammatory bowel disease.
European journal of gastroenterology & hepatology 2005 Jul 17 (7): 739-44. Mahmood Asif, Needham Jane, Prosser Jeanne, Mainwaring Jason, Trebble Tim, Mahy Gillian, Ramage Jo |
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Retinal vein occlusion: a form of venous thrombosis or a complication of atherosclerosis? A meta-analysis of thrombophilic factors.
Thrombosis and haemostasis 2005 Jun 93 (6): 1021-6. Janssen Mirian C H, den Heijer Martin, Cruysberg Johannes R M, Wollersheim Hub, Bredie Sebastian J |
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Cardiovascular and thrombophilic risk factors for idiopathic sudden sensorineural hearing loss.
Journal of thrombosis and haemostasis : JTH 2005 May 3 (5): 929-34. Marcucci R, Alessandrello Liotta A, Cellai A P, Rogolino A, Berloco P, Leprini E, Pagnini P, Abbate R, Prisco |
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Prevalence of antiphospholipid antibodies, factor V G1691A (Leiden) and prothrombin G20210A mutations in early and late recurrent pregnancy loss.
European journal of obstetrics, gynecology, and reproductive biology 2005 Apr 119 (2): 164-70. Mtiraoui Nabil, Borgi Lobna, Hizem Sondes, Nsiri Brahim, Finan Ramzi R, Gris Jean-Christophe, Almawi Wassim Y, Mahjoub Touha |
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Portal vein thrombosis in children and adolescents: the low prevalence of hereditary thrombophilic disorders.
Journal of pediatric surgery 2004 Sep 39 (9): 1356-61. Pinto Raquel B, Silveira Themis R, Bandinelli Eliane, Röhsig Lia |
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A C677T methylenetetrahydrofolate reductase (MTHFR) polymorphism and G20210A mutation in the prothrombin gene of sickle cell anemia patients from Northeast Brazil.
Hemoglobin 2004 Aug 28 (3): 237-41. Couto Fábio David, Boas Wendell Vilas, Lyra Isa, Zanette Angela, Dupuit Marie France, Almeida Mari Ney Tavares, Reis Mitermayer Galvão, Gonçalves Marilda Sou |
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Factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations among patients with sickle cell disease in Eastern Saudi Arabia.
American journal of hematology 2004 Jul 76 (3): 307-9. Fawaz Naglaa A, Bashawery Layla, Al-Sheikh Iman, Qatari Ahlam, Al-Othman Sara S, Almawi Wassim |
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Prothrombin gene mutation G20210A, homocysteine, antiphospholipid antibodies and other hypercoagulable states in ocular thrombosis.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2004 Jul 15 (5): 393-7. Van Cott Elizabeth M, Laposata Michael, Hartnett M Elizabe |
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An improved electronic microarray-based diagnostic assay for identification of MEFV mutations.
Human mutation 2004 Jun 23 (6): 621-8. Moutereau Stéphane, Narwa Rémy, Matheron Catherine, Vongmany Natalie, Simon Emmanuelle, Goossens Mich |
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Factor V G1691A, prothrombin G20210A, and methylenetetrahydrofolate reductase [MTHFR] C677T gene polymorphism in angiographically documented coronary artery disease.
Journal of thrombosis and thrombolysis 2004 Jun 17 (3): 199-205. Almawi Wassim Y, Ameen Ghada, Tamim Hala, Finan Ramzi R, Irani-Hakime No |
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Hyperhomocysteinemia and other thrombophilic risk factors in 26 patients with cerebral venous thrombosis.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2004 Jun 11 (6): 405-9. Boncoraglio G, Carriero M R, Chiapparini L, Ciceri E, Ciusani E, Erbetta A, Parati E |
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MTHFR C677T mutation, factor II G20210A mutation and factor V Leiden as risks factor for youth retinal vein occlusion.
La Clinica terapeutica 2004 154 (5): 299-303. Cruciani F, Moramarco A, Curto T, Labate A, Recupero V, Conti L, Gandolfo GM, Balacco Gabrieli C |
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The contribution of factor V Leiden and prothrombin G20210A mutation to the risk of central venous catheter-related thrombosis.
Haematologica 2004 Feb 89 (2): 201-6. Van Rooden CJ, Rosendaal FR, Meinders AE, Van Oostayen JA, Van Der Meer FJ, Huisman MV |
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Hyperhomocysteinemia and other newly recognized inherited coagulation disorders (factor V Leiden and prothrombin gene mutation) in patients with idiopathic cerebral vein thrombosis.
Cerebrovascular diseases (Basel, Switzerland) 2004 17 (2-3): 153-9. Ventura Paolo, Cobelli Milena, Marietta Marco, Panini Rossana, Rosa Maria Cristina, Salvioli Gianfran |
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Evaluation of the Roche LightCycler: a simple and rapid method for direct detection of factor V Leiden and prothrombin G20210A genotypes from blood samples without the need for DNA extraction.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2003 Jul 14 (5): 499-503. Cooper Peter C, Cooper Susan M, Smith Julie M, Kitchen Steven, Makris Micha |
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Genetic risk factors for cerebrovascular disease in children with sickle cell disease: design of a case-control association study and genomewide screen.
BMC medical genetics 2003 Jul 4 (): 6. Adams Gaye T, Snieder Harold, McKie Virgil C, Clair Betsy, Brambilla Donald, Adams Robert J, Kutlar Ferdane, Kutlar Abdull |
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[Occurrence of gene mutations in factor V Leiden, prothrombin and methylenetetrahydrofolate reductase in patients with pre-eclampsia].
Ceská gynekologie / Ceská lékarská spolecnost J. Ev. Purkyne 2003 May 68 (3): 162-6. Procházka M, Krcová V, Kudela M, Slavík |
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Combined carrier status of prothrombin 20210A and factor XIII-A Leu34 alleles as a strong risk factor for myocardial infarction: evidence of a gene-gene interaction.
Blood 2003 Apr 101 (8): 3037-41. Butt Christopher, Zheng Hong, Randell Edward, Robb Desmond, Parfrey Patrick, Xie Ya-Ga |
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Prothrombin G20210A mutation and oral contraceptive use increase upper-extremity deep vein thrombotic risk.
Thrombosis and haemostasis 2003 Mar 89 (3): 452-7. Vayá Amparo, Mira Yolanda, Mateo Jose, Falco Cristina, Villa Piedad, Estelles Amparo, Corella Dolores, Fontcuberta Jordi, Aznar Jus |
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Does the MTHFR 677T allele alter the clinical phenotype in severe haemophilia A?
Thrombosis research 2003 Jan 109 (1): 71-2. Ahmed Rafeeq, Kannan M, Choudhry Ved Prakash, Saxena Re |
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Interaction between hyperhomocysteinemia, mutated methylenetetrahydrofolatereductase (MTHFR) and inherited thrombophilic factors in recurrent venous thrombosis.
Thrombosis and haemostasis 2002 Nov 88 (5): 723-8. Keijzer Miranda B A J, den Heijer Martin, Blom Henk J, Bos Gerard M J, Willems Huub P J, Gerrits Wim B J, Rosendaal Frits |
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Effects of hereditary and acquired risk factors of venous thrombosis on a thrombin generation-based APC resistance test.
Thrombosis and haemostasis 2002 Jul 88 (1): 5-11. Curvers Joyce, Thomassen M Christella L G D, Rimmer Janet, Hamulyak Karly, van der Meer Jan, Tans Guido, Preston F Eric, Rosing J |
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Inherited thrombophilia and first venous thromboembolism during pregnancy and puerperium.
Thrombosis and haemostasis 2002 May 87 (5): 791-5. Martinelli Ida, De Stefano Valerio, Taioli Emanuela, Paciaroni Katia, Rossi Elena, Mannucci Pier Mannucc |
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Prothrombotic genotypes are not associated with pre-eclampsia and gestational hypertension: results from a large population-based study and systematic review.
Thrombosis and haemostasis 2002 May 87 (5): 779-85. Morrison E R, Miedzybrodzka Z H, Campbell D M, Haites N E, Wilson B J, Watson M S, Greaves M, Vickers M |
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Factor V Leiden (G1691A) and prothrombin gene G20210A mutations as potential risk factors for venous thromboembolism after total hip or total knee replacement surgery.
Thrombosis and haemostasis 2002 Apr 87 (4): 580-5. Wåhlander K, Larson G, Lindahl T L, Andersson C, Frison L, Gustafsson D, Bylock A, Eriksson B |
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[ABO/H blood groups and factor V Leiden].
Casopís lékar?? c?eských 2002 Mar 141 (5): 146-51. Matýsková M, Zavrelová J, Pejchalová A, Meluzinová H, Jank? |
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The prothrombin 20210A allele influences clinical manifestations of hemophilia A in patients with intron 22 inversion and without inhibitors.
Haematologica 2002 Mar 87 (3): 279-85. Tizzano Eduardo F, Soria José Manuel, Coll Immaculada, Guzmán Blanca, Cornet Mónica, Altisent Carmen, Martorell Marta, Domenech Montserrat, del Río Elisabeth, Fontcuberta Jordi, Baiget Montserr |
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Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations.
Haematologica 2002 Feb 87 (2): 177-81. Grandone Elvira, Margaglione Maurizio, Colaizzo Donatella, Pavone Giuseppe, Paladini Dario, Martinelli Pasquale, Di Minno Giovan |
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