HuGE Literature Finder
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Records 1-100
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Effect of prothrombotic genotypes on the risk of venous thromboembolism in patients with and without ischemic stroke.The TromsØ Study.
Journal of thrombosis and haemostasis : JTH 2019 Feb . Rinde Ludvig B, Morelli Vania M, Småbrekke Birgit, Mathiesen Ellisiv B, Løchen Maja-Lisa, Njølstad Inger, Wilsgaard Tom, Smith Erin, Rosendaal Frits R, Frazer Kelly A, Braekkan Sigrid K, Hansen John-Bjar |
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Thrombin-Activatable Fibrinolysis Inhibitor Polymorphisms and Cerebral Venous Thrombosis in Mexican Mestizo Patients.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2018 Nov 24 (8): 1291-1296. Arauz Antonio, Argüelles Nayelli, Jara Aurelio, Guerrero Jorge, Barboza Miguel |
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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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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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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 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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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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Identification of Genetic Aberrations in Thrombomodulin Gene in Patients With Recurrent Venous Thromboembolism.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2017 Jan 1076029616686716. Ahmad Abrar, Sundquist Kristina, Zöller Bengt, Svensson Peter J, Sundquist Jan, Memon Ashfaque |
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Prothrombin polymorphism A19911G, factor V HR2 haplotype A4070G, and plasminogen activator-inhibitor-1 polymorphism 4G/5G and the risk of retinal vein occlusion.
Ophthalmic genetics 2017 Jan 1-5. Kuhli-Hattenbach Claudia, Hellstern Peter, Nägler Dorit Karin, Kohnen Thomas, Hattenbach Lars-Ol |
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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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Identification of coagulation gene 3'UTR variants that are potentially regulated by microRNAs.
British journal of haematology 2017 06 177 (5): 782-790. Vossen Carla Y, van Hylckama Vlieg Astrid, Teruel-Montoya Raúl, Salloum-Asfar Salam, de Haan Hugoline, Corral Javier, Reitsma Pieter, Koeleman Bobby P C, Martínez Constanti |
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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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Genetic risk factors for venous thrombosis in women using combined oral contraceptives: update of the PILGRIM study.
Clinical genetics 2016 Jul . Suchon Pierre, Frouh Fadi Al, Ibrahim Manal, Sarlon Gabrielle, Venton Geoffroy, Alessi Marie-Christine, Trégouët David-Alexandre, Morange Pierre-Emmanu |
Genome-wide association analysis of self-reported events in 6135 individuals and 252 827 controls identifies 8 loci associated with thrombosis.
Human molecular genetics 2016 May 25 (9): 1867-74. Hinds David A, Buil Alfonso, Ziemek Daniel, Martinez-Perez Angel, Malik Rainer, Folkersen Lasse, Germain Marine, Mälarstig Anders, Brown Andrew, Soria Jose Manuel, Dichgans Martin, Bing Nan, Franco-Cereceda Anders, Souto Juan Carlos, Dermitzakis Emmanouil T, Hamsten Anders, Worrall Bradford B, Tung Joyce Y, , Sabater-Lleal Mar |
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Global prevalence of prothrombin gene mutation G20210A and implications in women's health: a systematic review.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2016 Apr . Dziadosz Margaret, Baxi Laxmi |
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Homozygous Carrier of Prothrombin G20210A Mutation with Massive Pulmonary Embolism and His Family: Gender Differences of Susceptibility to Mutation.
Folia medica 2016 Mar 58 (1): 64-6. Stoeva Natalia Y, Koleva Vessela |
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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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Genetic risk factors for venous thrombosis in the elderly in a case-control study.
Journal of thrombosis and haemostasis : JTH 2016 09 14 (9): 1759-64. Karasu A, Engbers M J, Cushman M, Rosendaal F R, van Hylckama Vlieg |
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Prothrombin gene 20210A mutation in Slovak population.
Vnitrni lekarstvi 2016 62 (4): 281-286. Chudej Juraj, Plame?ová Iva |
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Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis.
PloS one 2016 11 (3): e0151347. Gorski Marcin M, Lotta Luca A, Pappalardo Emanuela, de Haan Hugoline G, Passamonti Serena M, van Hylckama Vlieg Astrid, Martinelli Ida, Peyvandi Flo |
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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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F11 is associated with recurrent VTE in women. A prospective cohort study.
Thrombosis and haemostasis 2015 Oct 115 (2): . Bruzelius M, Ljungqvist M, Bottai M, Bergendal A, Strawbridge R J, Holmström M, Silveira A, Kieler H, Hamsten A, Lärfars G, Odeberg |
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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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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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The Prevalence of the Prothrombin (F2) 20210G>A Mutation in a Cohort of Sri Lankan Patients with Thromboembolic Disorders.
Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2015 Sep 31 (3): 356-61. Gunathilake K M D, Sirisena U N D, Nisansala P K D, Goonasekera H W W, Jayasekara R W, Dissanayake V H |
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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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Genetic Risk Factors of Venous Thromboembolism in the East Algerian Population.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2015 Aug . Moussaoui S, Saussoy P, Ambroise J, Defour J P, Zouitene R, Sifi K, Abadi |
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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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Thrombophilic factor analysis in cirrhotic patients with portal vein thrombosis.
Journal of thrombosis and thrombolysis 2015 Jul 40 (1): 54-60. Saugel Bernd, Lee Marcel, Feichtinger Stephanie, Hapfelmeier Alexander, Schmid Roland M, Siveke Jens |
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Testosterone, thrombophilia, thrombosis.
Translational research : the journal of laboratory and clinical medicine 2015 May 165 (5): 537-48. Freedman Joel, Glueck Charles J, Prince Marloe, Riaz Rashid, Wang Pi |
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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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Meta-analysis of 65,734 individuals identifies TSPAN15 and SLC44A2 as two susceptibility loci for venous thromboembolism.
American journal of human genetics 2015 Apr 96 (4): 532-42. Germain Marine, Chasman Daniel I, de Haan Hugoline, Tang Weihong, Lindström Sara, Weng Lu-Chen, de Andrade Mariza, de Visser Marieke C H, Wiggins Kerri L, Suchon Pierre, Saut Noémie, Smadja David M, Le Gal Grégoire, van Hylckama Vlieg Astrid, Di Narzo Antonio, Hao Ke, Nelson Christopher P, Rocanin-Arjo Ares, Folkersen Lasse, Monajemi Ramin, Rose Lynda M, Brody Jennifer A, Slagboom Eline, Aïssi Dylan, Gagnon France, Deleuze Jean-Francois, Deloukas Panos, Tzourio Christophe, Dartigues Jean-Francois, Berr Claudine, Taylor Kent D, Civelek Mete, Eriksson Per, , Psaty Bruce M, Houwing-Duitermaat Jeanine, Goodall Alison H, Cambien François, Kraft Peter, Amouyel Philippe, Samani Nilesh J, Basu Saonli, Ridker Paul M, Rosendaal Frits R, Kabrhel Christopher, Folsom Aaron R, Heit John, Reitsma Pieter H, Trégouët David-Alexandre, Smith Nicholas L, Morange Pierre-Emmanu |
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Determinants of premature familial arterial thrombosis in patients with juvenile ischaemic stroke. The Italian Project on Stroke in Young Adults (IPSYS).
Thrombosis and haemostasis 2015 Mar 113 (3): 641-8. Pezzini Alessandro, Grassi Mario, Lodigiani Corrado, Patella Rosalba, Gandolfo Carlo, Zini Andrea, DeLodovici Maria Luisa, Paciaroni Maurizio, Del Sette Massimo, Toriello Antonella, Musolino Rossella, Calabrò Rocco Salvatore, Bovi Paolo, Adami Alessandro, Silvestrelli Giorgio, Sessa Maria, Cavallini Anna, Marcheselli Simona, Bonifati Domenico Marco, Checcarelli Nicoletta, Tancredi Lucia, Chiti Alberto, Del Zotto Elisabetta, Spalloni Alessandra, Costa Paolo, Giacalone Giacomo, Ferrazzi Paola, Poli Loris, Morotti Andrea, Rasura Maurizia, Simone Anna Maria, Gamba Massimo, Cerrato Paolo, Micieli Giuseppe, Melis Maurizio, Massucco Davide, De Giuli Valeria, Pepe Daniele, Iacoviello Licia, Padovani Alessandro, |
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Causes and consequences of portal vein thrombosis in 1,243 patients with cirrhosis: results of a longitudinal study.
Hepatology (Baltimore, Md.) 2015 Feb 61 (2): 660-7. Nery Filipe, Chevret Sylvie, Condat Bertrand, de Raucourt Emmanuelle, Boudaoud Larbi, Rautou Pierre-Emmanuel, Plessier Aurelie, Roulot Dominique, Chaffaut Cendrine, Bourcier Valerie, Trinchet Jean-Claude, Valla Dominique-Charles, |
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Predicting venous thrombosis in women using a combination of genetic markers and clinical risk factors.
Journal of thrombosis and haemostasis : JTH 2015 Feb 13 (2): 219-27. Bruzelius M, Bottai M, Sabater-Lleal M, Strawbridge R J, Bergendal A, Silveira A, Sundström A, Kieler H, Hamsten A, Odeberg |
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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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Genetic variations associated with recurrent venous thrombosis.
Circulation. Cardiovascular genetics 2014 Dec 7 (6): 806-13. van Hylckama Vlieg Astrid, Flinterman Linda E, Bare Lance A, Cannegieter Suzanne C, Reitsma Pieter H, Arellano Andre R, Tong Carmen H, Devlin James J, Rosendaal Frits |
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Associations of coagulation factor V Leiden and prothrombin G20210A mutations with Budd-Chiari syndrome and portal vein thrombosis: a systematic review and meta-analysis.
Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association 2014 Nov 12 (11): 1801-12.e7. Qi Xingshun, Ren Weirong, De Stefano Valerio, Fan Daimi |
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Factor V Leiden 1691G/A and prothrombin gene 20210G/A polymorphisms as prothrombotic markers in adult Egyptian acute leukemia patients.
Medical oncology (Northwood, London, England) 2014 Nov 31 (11): 265. El Sissy Azza Hamdy, El Sissy Maha H, Elmoamly Shere |
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Multilocus genetic risk scores for venous thromboembolism risk assessment.
Journal of the American Heart Association 2014 Oct 3 (5): e001060. Soria José Manuel, Morange Pierre-Emmanuel, Vila Joan, Souto Juan Carlos, Moyano Manel, Trégouët David-Alexandre, Mateo José, Saut Noémi, Salas Eduardo, Elosua Rober |
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Circulating microparticles in carriers of prothrombin G20210A mutation.
Thrombosis and haemostasis 2014 Sep 112 (3): 432-7. Campello E, Spiezia L, Radu C M, Gavasso S, Zerbinati P, Woodhams B, Simioni |
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Factors that predict thrombosis in relatives of patients with venous thromboembolism.
Blood 2014 Sep 124 (13): 2124-30. Couturaud Francis, Leroyer Christophe, Tromeur Cecile, Julian Jim A, Kahn Susan R, Ginsberg Jeffrey S, Wells Philip S, Douketis James D, Mottier Dominique, Kearon Cli |
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Thrombophilic risk factors in different types of retinal vein occlusion in Tunisian patients.
Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association 2014 Jul 23 (6): 1592-8. Mrad Meriem, Fekih-Mrissa Najiba, Wathek Cheima, Rannen Riadh, Gabsi Salem, Gritli Nasreddi |
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Association between inherited thrombophilia and impaired right ventricular function in deep vein thrombosis without symptomatic pulmonary embolism.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2014 Apr 20 (3): 270-7. Asgun Halil Fatih, Kirilmaz Bahadir, Saygi Serkan, Ozturk Okan, Silan Fatma, Karatag Ozan, Kosar Sule, Ozdemir Oztu |
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Impact of coagulation in the development of thromboembolic events in patients with spinal cord injury.
Spinal cord 2014 Apr 52 (4): 327-32. de Campos Guerra J C, Mourão M A, França C N, da Rosa C D P, Burattini M |
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Association between thrombophilia and seated immobility venous thromboembolism.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2014 Mar 25 (2): 135-41. Siniarski Aleksander, Wypasek Ewa, Fijorek Kamil, Gajos Grzegorz, Undas Anet |
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Influence of single nucleotide polymorphisms on thrombin generation in factor V Leiden heterozygotes.
Thrombosis and haemostasis 2014 Mar 111 (3): 438-46. Segers O, Simioni P, Tormene D, Castoldi |
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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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Risk assessment of venous thrombosis in families with known hereditary thrombophilia: the MARseilles-NImes prediction model.
Journal of thrombosis and haemostasis : JTH 2014 Feb 12 (2): 138-146. Cohen W, Castelli C, Suchon P, Bouvet S, Aillaud M F, Brunet D, Barthet M C, Alessi M C, Trégouët D A, Morange P |
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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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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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Risk of Budd-Chiari syndrome associated with factor V Leiden and G20210A prothrombin mutation: a meta-analysis.
PloS one 2014 9 (4): e95719. Zhang Peijin, Zhang Jing, Sun Guixiang, Gao Xiuyin, Wang Hui, Yan Wenjun, Xu Hao, Zu Maoheng, Ma He, Wang Wei, Lu Zhaoj |
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The 3'end prothrombin gene variants in patients with different thrombotic events.
Laboratory medicine 2014 45 (4): 309-14. Djordjevic Valentina, Pruner Iva, Tomic Branko, Nestorovic Aleksandra, Gvozdenov Maja, Kovac Mirjana, Radojkovic Dragi |
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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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High prevalence of prothrombotic abnormalities in multifocal osteonecrosis: description of a series and review of the literature.
Medicine 2013 Nov 92 (6): 295-304. Gómez-Puerta Jose A, Peris Pilar, Reverter Joan Carles, Espinosa Gerard, Martinez-Ferrer Angeles, Monegal Ana, Monteagudo Juan, Tàssies Dolors, Guañabens Nur |
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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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Homozygous factor V Leiden and double heterozygosity for factor V Leiden and prothrombin mutation.
Journal of thrombosis and thrombolysis 2013 Oct 36 (3): 324-31. Saemundsson Ymir, Sveinsdottir Signý Vala, Svantesson Henrik, Svensson Peter |
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Influence of proband's characteristics on the risk for venous thromboembolism in relatives with factor V Leiden or prothrombin G20210A polymorphisms.
Blood 2013 Oct 122 (15): 2555-61. Bucciarelli Paolo, De Stefano Valerio, Passamonti Serena M, Tormene Daniela, Legnani Cristina, Rossi Elena, Castaman Giancarlo, Simioni Paolo, Cini Michela, Martinelli I |
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Clinical and genetic factors associated with venous thromboembolism in myeloma patients treated with lenalidomide-based regimens.
American journal of hematology 2013 Sep 88 (9): 765-70. Bagratuni Tina, Kastritis Efstathios, Politou Marianna, Roussou Maria, Kostouros Efthimios, Gavriatopoulou Maria, Eleutherakis-Papaiakovou Evangelos, Kanelias Nikolaos, Terpos Evangelos, Dimopoulos Meletios |
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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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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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Screening for coagulopathy and identification of children with acute lymphoblastic leukemia at a higher risk of symptomatic venous thrombosis: an AIEOP experience.
Journal of pediatric hematology/oncology 2013 Jul 35 (5): 348-55. Santoro Nicola, Colombini Antonella, Silvestri Daniela, Grassi Massimo, Giordano Paola, Parasole Rosanna, Barisone Elena, Caruso Roberta, Conter Valentino, Valsecchi Maria G, Masera Giuseppe, Rizzari Carme |
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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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Non-steroidal anti-inflammatory drugs and venous thromboembolism in women.
Pharmacoepidemiology and drug safety 2013 Jun 22 (6): 658-66. Bergendal Annica, Adami Johanna, Bahmanyar Shahram, Hedenmalm Karin, Lärfars Gerd, Persson Ingemar, Sundström Anders, Kieler Hel |
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Venous thromboembolism in patients with Cushing's syndrome: need of a careful investigation of the prothrombotic risk profile.
Pituitary 2013 Jun 16 (2): 175-81. Koutroumpi S, Daidone V, Sartori M T, Cattini M G, Albiger N M, Occhi G, Ferasin S, Frigo A, Mantero F, Casonato A, Scaroni |
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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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ABO blood groups and the risk of venous thrombosis in patients with inherited thrombophilia.
Blood transfusion = Trasfusione del sangue 2013 Apr 11 (2): 250-3. Spiezia Luca, Campello Elena, Bon Maria, Tison Tiziana, Milan Marta, Simioni Paolo, Prandoni Pao |
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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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Retinal vein occlusion: genetic predisposition and systemic risk factors.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Apr 24 (3): 279-83. Giannaki Kassiani, Politou Marianna, Rouvas Alexandros, Merkouri Efrossyni, Travlou Anthi, Theodosiadis Panayiotis, Gialeraki Argy |
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Thrombophilia and varicella zoster in children.
Hematology (Amsterdam, Netherlands) 2013 Mar 18 (2): 119-22. Ferrara Mara, Bertocco F, Ferrara D, Capozzi |
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Risk of venous thromboembolism and myocardial infarction associated with factor V Leiden and prothrombin mutations and blood type.
CMAJ : Canadian Medical Association journal = journal de l'Association medicale canadienne 2013 Feb . Sode BF, Allin KH, Dahl M, Gyntelberg F, Nordestgaard BG |
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Genetic Polymorphisms Associated with Retinal Vein Occlusion: A Greek Case-control Study and Meta-analysis.
Ophthalmic genetics 2013 Jan . Yioti GG, Panagiotou OA, Vartholomatos GA, Kolaitis NI, Pappa CN, Evangelou E, Stefaniotou MI |
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PLA2 polymorphism of platelet glycoprotein IIb/IIIa but not Factor V Leiden and prothrombin G20210A polymorphisms is associated with venous thromboembolism and more recurrent events in central Iran.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2013 Jan . Pourgheysari B, Boroujeni HR, Hasheminia AM, Drees F |
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Polymorphisms in Factor II and Factor V thrombophilia genes among Circassians in Jordan.
Journal of thrombosis and thrombolysis 2013 Jan 35 (1): 83-9. Dajani R, Arafat A, Hakooz N, Al-Abbadi Z, Yousef Al-Motassem, El Khateeb M, Quadan |
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The influence of factor V Leiden and G20210A prothrombin mutation on the presence of residual vein obstruction after idiopathic deep-vein thrombosis of the lower limbs.
Thrombosis and haemostasis 2013 Jan 109 (3): 3. Cosmi B, Legnani C, Pengo V, Ghirarduzzi A, Testa S, Poli D, Prisco D, Tripodi A, Palareti G |
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The influence of thrombophilic risk factors on vascular access survival in chronic dialysis patients in a retrospective evaluation.
VASA. Zeitschrift für Gefässkrankheiten 2013 Jan 42 (1): 32-9. Klamroth Robert, Orlovic Marija, Fritsche Ilona, Seibt Simone, Seibt Frank, Wegscheider Karl, Landgraf Helm |
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The Risk Factors for Thrombosis in Children With Acute Lymphoblastic Leukemia.
Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis 2013 Jan . Sivaslioglu S, Gursel T, Kocak U, Kaya Z |
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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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Prevalence of variants that confer risk for venous thromboembolism in an elderly population of northeastern Brazil.
Genetics and molecular research : GMR 2013 12 (3): 3698-707. Ferreira-Fernandes H, Costa P N, Fernandes H F, Araújo-Neto A P, Motta F J, Canalle R, Yoshioka F K, Guerreiro J F, Burbano R R, Rey J A, Pinto G |
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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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Prothrombotic polymorphisms in patients with Raynaud's phenomenon and migraine.
Acta physiologica Hungarica 2012 Dec 99 (4): 4. Takáts AT, Shemirani AH, Zsóri KS, András C, Csiki Z |
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Association of Allelic Variants of Factor V Leiden, Prothrombin And Methylenetetrahydrofolate Reductase with Thrombosis Or Ocular Involvement In Behçet's Disease: A Systematic Review And Meta-Analysis.
Autoimmunity reviews 2012 Nov . Chamorro AJ, Marcos M, Hernández-García I, Calvo A, Mejia JC, Cervera R, Espinosa G |
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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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Does asymptomatic carriage of FV Leiden and FII prothrombin mutations in heterozygous configuration pose an increased risk of thrombembolic complications in the course of pregnancy, labor and puerperium?
Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia 2012 Oct . Vavrinkova B, Binder T, Hadacova I, Hrachovinova I, Salaj P, Hruda M |
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Extrahepatic portal venous system thrombosis in recurrent acute and chronic alcoholic pancreatitis is caused by local inflammation and not thrombophilia.
The American journal of gastroenterology 2012 Oct 107 (10): 1579-85. Rebours Vinciane, Boudaoud Larbi, Vullierme Marie-Pierre, Vidaud Dominique, Condat Bertrand, Hentic Olivia, Maire Frédérique, Hammel Pascal, Ruszniewski Philippe, Lévy Philip |
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High prevalence of three prothrombotic polymorphisms among Palestinians: factor V G1691A, factor II G20210A and methylenetetrahydrofolate reductase C677T.
Journal of thrombosis and thrombolysis 2012 Oct 34 (3): 383-7. Hussein Ayman |
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Do thrombophilic gene mutations have a role on thromboembolic events in cancer patients?
Asia-Pacific journal of clinical oncology 2012 Sep 8 (3): e34-41. Ozkan Metin, Sivgin Serdar, Kocyigit Ismail, Emirogullari Funda, Dikilitas Mustafa, Kaynar Leylagul, Ozkul Yusuf, Er Ozl |
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Low borderline plasma levels of antithrombin, protein C and protein S are risk factors for venous thromboembolism.
Journal of thrombosis and haemostasis : JTH 2012 Sep 10 (9): 1783-91. Bucciarelli P, Passamonti S M, Biguzzi E, Gianniello F, Franchi F, Mannucci P M, Martinelli |
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Risk of placenta-mediated pregnancy complications or pregnancy-related VTE in VTE-asymptomatic families of probands with VTE and heterozygosity for factor V Leiden or G20210 prothrombin mutation.
European journal of haematology 2012 Sep 89 (3): 250-5. Cordoba Iris, Pegenaute Carlota, González-López Tomás José, Chillon Carmen, Sarasquete Maria Eugenia, Martin-Herrero Francisco, Guerrero Carmen, Cabrero Mónica, Garcia Sanchez Maria Helena, Pabon Pedro, Lozano Francisco Santiago, Gonzalez Marcos, Alberca Ignacio, González-Porras José Ram |
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The G534E-polymorphism of the gene encoding the factor VII-activating protease is a risk factor for venous thrombosis and recurrent events.
Thrombosis research 2012 Sep 130 (3): 441-4. Ahmad-Nejad Parviz, Dempfle Carl-Erik, Weiss Christel, Bugert Peter, Borggrefe Martin, Neumaier Micha |
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Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2012 Sep 19 (9): 1326-7. Ben Salem-Berrabah Olfa, Fekih-Mrissa Nejiba, N'siri Brahim, Ben Hamida Abdelmajid, Benammar-Elgaaied Amel, Gritli Nasreddine, Mrissa Rid |
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[The mutation of genes of hemostasis system in patients with venous cerebral angiodystonia against the background of connective tissue dysplasia].
Klinicheskaia laboratornaia diagnostika 2012 Aug (8): 33-6. Kotovshchikova E F, Buevich E I, Pen'kova E V, Kulikov V P, Chudimov V F, Siul'zhina E N, Bogdanova I V, Bochkarev A |
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A genome-wide association study of venous thromboembolism identifies risk variants in chromosomes 1q24.2 and 9q.
Journal of thrombosis and haemostasis : JTH 2012 Aug 10 (8): 1521-31. Heit J A, Armasu S M, Asmann Y W, Cunningham J M, Matsumoto M E, Petterson T M, De Andrade |
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ABO blood group and von Willebrand factor levels partially explained the incomplete penetrance of congenital thrombophilia.
Arteriosclerosis, thrombosis, and vascular biology 2012 Aug 32 (8): 2021-8. Cohen William, Castelli Christel, Alessi Marie-Christine, Aillaud Marie-Françoise, Bouvet Sophie, Saut Noémie, Brunet Dominique, Barthet Marie-Christine, Tregouet David-Alexandre, Lavigne Géraldine, Morange Pierre-Emmanu |
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