HuGE Literature Finder
Records 1-30
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Prothrombotic genotypes and risk of major bleeding in patients with incident venous thromboembolism.
Thrombosis research 2020 Apr 191 82-89. Johnsen Håkon S, Bjøri Esben, Hindberg Kristian, Brækkan Sigrid K, Morelli Vânia M, Hansen John-Bjar |
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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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Targeted sequencing to identify novel genetic risk factors for deep vein thrombosis: a study of 734 genes.
Journal of thrombosis and haemostasis : JTH 2018 Aug . de Haan H G, van Hylckama Vlieg A, Lotta L A, Gorski Marcin M, Bucciarelli P, Martinelli I, , Baglin T P, Peyvandi F, Rosendaal F |
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Venous thromboembolism risk associated with ABO, F11 and FGG loci.
Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis 2018 Jul . Manco Licínio, Silva Catarina, Fidalgo Teresa, Martinho Patrícia, Sarmento Ana B, Ribeiro M Letíc |
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Impact of baseline clinical and laboratory features on the risk of thrombosis in children with acute lymphoblastic leukemia: A prospective evaluation.
Pediatric blood & cancer 2018 Jan . Athale Uma H, Mizrahi T, Laverdière C, Nayiager T, Delva Y-L, Foster G, Thabane L, David M, Leclerc J-M, Chan A K |
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Joint effects of prothrombotic genotypes and body height on the risk of venous thromboembolism: The Tromsø Study.
Journal of thrombosis and haemostasis : JTH 2017 Nov . Horvei Lars D, Braekkan Sigrid K, Smith Erin N, Solomon Terry, Hindberg Kristian, Frazer Kelly A, Rosendaal Frits R, Hansen John-Bjar |
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Polymorphism of the ABO gene associate with thrombosis risk in patients with paroxysmal nocturnal hemoglobinuria.
Oncotarget 2017 Nov 8 (54): 92411-92419. Long Zhangbiao, Du Yali, Li Hongmin, Han Bi |
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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 |
Genetic Analysis of Venous Thromboembolism in UK Biobank Identifies the ZFPM2 Locus and Implicates Obesity as a Causal Risk Factor.
Circulation. Cardiovascular genetics 2017 Apr 10 (2): . Klarin Derek, Emdin Connor A, Natarajan Pradeep, Conrad Mark F, , Kathiresan Sek |
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A comprehensive survey of genetic variation in 20,691 subjects from four large cohorts.
PloS one 2017 12 (3): e0173997. Lindström Sara, Loomis Stephanie, Turman Constance, Huang Hongyan, Huang Jinyan, Aschard Hugues, Chan Andrew T, Choi Hyon, Cornelis Marilyn, Curhan Gary, De Vivo Immaculata, Eliassen A Heather, Fuchs Charles, Gaziano Michael, Hankinson Susan E, Hu Frank, Jensen Majken, Kang Jae H, Kabrhel Christopher, Liang Liming, Pasquale Louis R, Rimm Eric, Stampfer Meir J, Tamimi Rulla M, Tworoger Shelley S, Wiggs Janey L, Hunter David J, Kraft Pet |
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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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Genome-wide studies of von Willebrand factor propeptide identify loci contributing to variation in propeptide levels and von Willebrand factor clearance.
Journal of thrombosis and haemostasis : JTH 2016 09 14 (9): 1888-98. Ozel A B, McGee B, Siemieniak D, Jacobi P M, Haberichter S L, Brody L C, Mills J L, Molloy A M, Ginsburg D, Li J Z, Desch K |
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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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Replication of a genetic risk score for venous thromboembolism in whites but not in African Americans.
Journal of thrombosis and haemostasis : JTH 2015 Nov . Folsom Aaron R, Tang Weihong, Weng Lu-Chen, Roetker Nicholas S, Cushman Mary, Basu Saonli, Pankow James |
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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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Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.
American journal of hematology 2015 Jun 90 (6): 534-40. Tang Weihong, Cushman Mary, Green David, Rich Stephen S, Lange Leslie A, Yang Qiong, Tracy Russell P, Tofler Geoffrey H, Basu Saonli, Wilson James G, Keating Brendan J, Weng Lu-Chen, Taylor Herman A, Jacobs David R, Delaney Joseph A, Palmer Cameron D, Young Taylor, Pankow James S, O'Donnell Christopher J, Smith Nicholas L, Reiner Alexander P, Folsom Aaron |
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ABO blood type and ABO gene with susceptibility to deep vein thrombosis following orthopedic surgery: a case-control study in Chinese Han population.
Science China. Life sciences 2015 Apr 58 (4): 390-1. Sun Ye, Mao Ping, Lu JingWei, Dai Jin, Teng HuaJian, Jiang Qi |
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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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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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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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Influence of coronary artery disease-associated genetic variants on risk of venous thromboembolism.
Thrombosis research 2014 Aug 134 (2): 426-32. Bruzelius Maria, Strawbridge Rona J, Trégouët David-Alexandre, Wiggins Kerri L, Gertow Karl, Sabater-Lleal Maria, Öhrvik John, Bergendal Annica, Silveira Angela, Sundström Anders, Kieler Helle, Syvänen Ann-Christine, Smith Nicholas L, Morange Pierre-Emmanuel, Odeberg Jacob, Hamsten Ande |
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ABO blood group polymorphisms and risk for ischemic stroke and peripheral arterial disease.
Molecular biology reports 2014 Mar 41 (3): 1771-7. Sabino Adriano de Paula, Ribeiro Daniel Dias, Domingheti Caroline Pereira, Rios Danyelle Romana Alves, Dusse Luci Maria SantAna, Carvalho Maria das Graças, Fernandes Ana Pau |
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Lack of strong effect modification by NFE2L2/CYP3A5/ABO of the risk of venous thrombosis associated with oral hormone therapy.
Journal of thrombosis and haemostasis : JTH 2013 Aug 11 (8): 1617-9. Blondon M, Wiggins K L, Harrington L B, Psaty B M, Smith N |
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A genome-wide association study for venous thromboembolism: the extended cohorts for heart and aging research in genomic epidemiology (CHARGE) consortium.
Genetic epidemiology 2013 Jul 37 (5): 512-21. Tang Weihong, Teichert Martina, Chasman Daniel I, Heit John A, Morange Pierre-Emmanuel, Li Guo, Pankratz Nathan, Leebeek Frank W, Paré Guillaume, de Andrade Mariza, Tzourio Christophe, Psaty Bruce M, Basu Saonli, Ruiter Rikje, Rose Lynda, Armasu Sebastian M, Lumley Thomas, Heckbert Susan R, Uitterlinden André G, Lathrop Mark, Rice Kenneth M, Cushman Mary, Hofman Albert, Lambert Jean-Charles, Glazer Nicole L, Pankow James S, Witteman Jacqueline C, Amouyel Philippe, Bis Joshua C, Bovill Edwin G, Kong Xiaoxiao, Tracy Russell P, Boerwinkle Eric, Rotter Jerome I, Trégouët David-Alexandre, Loth Daan W, Stricker Bruno H Ch, Ridker Paul M, Folsom Aaron R, Smith Nicholas |
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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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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 carotid artery intima-media thickness and coronary artery calcification in women of the Kronos Early Estrogen Prevention Study.
Physiological genomics 2013 Jan 45 (2): 79-88. Miller Virginia M, Petterson Tanya M, Jeavons Elysia N, Lnu Abhinita S, Rider David N, Heit John A, Cunningham Julie M, Huggins Gordon S, Hodis Howard N, Budoff Matthew J, Santoro Nanette, Hopkins Paul N, Lobo Rogerio A, Manson JoAnn E, Naftolin Frederick, Taylor Hugh S, Harman S Mitchell, de Andrade Mari |
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Linkage analysis identifies a locus for plasma von Willebrand factor undetected by genome-wide association.
Proceedings of the National Academy of Sciences of the United States of America 2013 Jan 110 (2): 588-93. Desch Karl C, Ozel Ayse B, Siemieniak David, Kalish Yossi, Shavit Jordan A, Thornburg Courtney D, Sharathkumar Anjali A, McHugh Caitlin P, Laurie Cathy C, Crenshaw Andrew, Mirel Daniel B, Kim Yoonhee, Cropp Cheryl D, Molloy Anne M, Kirke Peadar N, Bailey-Wilson Joan E, Wilson Alexander F, Mills James L, Scott John M, Brody Lawrence C, Li Jun Z, Ginsburg Dav |
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Single nucleotide polymorphisms and the risk of venous thrombosis: results from a Danish case-cohort study.
British journal of haematology 2012 Nov . El-Galaly TC, Severinsen MT, Overvad K, Steffensen R, Vistisen AK, Tjønneland A, Kristensen SR |
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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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Genetic associations for activated partial thromboplastin time and prothrombin time, their gene expression profiles, and risk of coronary artery disease.
American journal of human genetics 2012 Jul 91 (1): 152-62. Tang Weihong, Schwienbacher Christine, Lopez Lorna M, Ben-Shlomo Yoav, Oudot-Mellakh Tiphaine, Johnson Andrew D, Samani Nilesh J, Basu Saonli, Gögele Martin, Davies Gail, Lowe Gordon D O, Tregouet David-Alexandre, Tan Adrian, Pankow James S, Tenesa Albert, Levy Daniel, Volpato Claudia B, Rumley Ann, Gow Alan J, Minelli Cosetta, Yarnell John W G, Porteous David J, Starr John M, Gallacher John, Boerwinkle Eric, Visscher Peter M, Pramstaller Peter P, Cushman Mary, Emilsson Valur, Plump Andrew S, Matijevic Nena, Morange Pierre-Emmanuel, Deary Ian J, Hicks Andrew A, Folsom Aaron |
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Non-O blood type is the commonest genetic risk factor for VTE: results from a meta-analysis of the literature.
Seminars in thrombosis and hemostasis 2012 Jul 38 (5): 535-48. Dentali Francesco, Sironi Anna Paola, Ageno Walter, Turato Sara, Bonfanti Carlo, Frattini Francesco, Crestani Silvia, Franchini Massi |
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The association of non-O blood group and severity of liver fibrosis in patients with chronic hepatitis C infection.
Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences 2012 May 17 (5): 466-9. Shavakhi Ahmad, Hajalikhani Mehri, Minakari Mohammad, Norian Alireza, Riahi Rahil, Azarnia Mina, Liaghat Li |
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Human metabolic individuality in biomedical and pharmaceutical research.
Nature 2011 Sep 477 (7362): 54-60. Suhre Karsten, Shin So-Youn, Petersen Ann-Kristin, Mohney Robert P, Meredith David, Wägele Brigitte, Altmaier Elisabeth, , Deloukas Panos, Erdmann Jeanette, Grundberg Elin, Hammond Christopher J, de Angelis Martin Hrabé, Kastenmüller Gabi, Köttgen Anna, Kronenberg Florian, Mangino Massimo, Meisinger Christa, Meitinger Thomas, Mewes Hans-Werner, Milburn Michael V, Prehn Cornelia, Raffler Johannes, Ried Janina S, Römisch-Margl Werner, Samani Nilesh J, Small Kerrin S, Wichmann H-Erich, Zhai Guangju, Illig Thomas, Spector Tim D, Adamski Jerzy, Soranzo Nicole, Gieger Christi |
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Genetic variation within the anticoagulant, procoagulant, fibrinolytic and innate immunity pathways as risk factors for venous thromboembolism.
Journal of thrombosis and haemostasis : JTH 2011 Jun 9 (6): 1133-42. Heit J A, Cunningham J M, Petterson T M, Armasu S M, Rider D N, DE Andrade |
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Hemodialysis vascular access thrombosis: The role of factor V Leiden, prothrombin gene mutation and ABO blood groups.
Clinica chimica acta; international journal of clinical chemistry 2011 Feb 412 (5-6): 425-9. Rios Danyelle R A, Fernandes Ana P, Carvalho Maria G, Figueiredo Roberta C, Guimarães Daniela A M, Reis Daniberg R, Simões e Silva Ana C, Gomes Karina B, Dusse Luci M |
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Genetics of venous thrombosis: insights from a new genome wide association study.
PloS one 2011 6 (9): e25581. Germain Marine, Saut Noémie, Greliche Nicolas, Dina Christian, Lambert Jean-Charles, Perret Claire, Cohen William, Oudot-Mellakh Tiphaine, Antoni Guillemette, Alessi Marie-Christine, Zelenika Diana, Cambien François, Tiret Laurence, Bertrand Marion, Dupuy Anne-Marie, Letenneur Luc, Lathrop Mark, Emmerich Joseph, Amouyel Philippe, Trégouët David-Alexandre, Morange Pierre-Emmanu |
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Effect of genetic variations in syntaxin-binding protein-5 and syntaxin-2 on von Willebrand factor concentration and cardiovascular risk.
Circulation. Cardiovascular genetics 2010 Dec 3 (6): 507-12. van Loon Janine E, Leebeek Frank W G, Deckers Jaap W, Dippel Diederik W J, Poldermans Don, Strachan David P, Tang Weihong, O'Donnell Christopher J, Smith Nicholas L, de Maat Moniek P |
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von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.
Journal of thrombosis and haemostasis : JTH 2010 Sep 8 (9): 1986-93. Hickson N, Hampshire D, Winship P, Goudemand J, Schneppenheim R, Budde U, Castaman G, Rodeghiero F, Federici A B, James P, Peake I, Eikenboom J, Goodeve A, |
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Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) Consortium.
Circulation 2010 Mar 121 (12): 1382-92. Smith Nicholas L, Chen Ming-Huei, Dehghan Abbas, Strachan David P, Basu Saonli, Soranzo Nicole, Hayward Caroline, Rudan Igor, Sabater-Lleal Maria, Bis Joshua C, de Maat Moniek P M, Rumley Ann, Kong Xiaoxiao, Yang Qiong, Williams Frances M K, Vitart Veronique, Campbell Harry, Mälarstig Anders, Wiggins Kerri L, Van Duijn Cornelia M, McArdle Wendy L, Pankow James S, Johnson Andrew D, Silveira Angela, McKnight Barbara, Uitterlinden Andre G, , Aleksic Nena, Meigs James B, Peters Annette, Koenig Wolfgang, Cushman Mary, Kathiresan Sekar, Rotter Jerome I, Bovill Edwin G, Hofman Albert, Boerwinkle Eric, Tofler Geoffrey H, Peden John F, Psaty Bruce M, Leebeek Frank, Folsom Aaron R, Larson Martin G, Spector Timothy D, Wright Alan F, Wilson James F, Hamsten Anders, Lumley Thomas, Witteman Jacqueline C M, Tang Weihong, O'Donnell Christopher |
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ABO blood groups and genetic risk factors for thrombosis in Croatian population.
Croatian medical journal 2009 Dec 50 (6): 550-8. Jukic Irena, Bingulac-Popovic Jasna, Dogic Vesna, Babic Ivana, Culej Jelena, Tomicic Maja, Vuk Tomislav, Sarlija Dorotea, Balija Meli |
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Perioperative genomic profiles using structure-specific oligonucleotide probes.
Clinical medicine & research 2009 Sep 7 (3): 69-84. Hogan Kirk J, Burmester James K, Caldwell Michael D, Hogan Quinn H, Coursin Douglas B, Green Dawn N, Selzer Rebecca M R, Broderick Thomas P, Rusy Deborah A, Poroli Mark, Lutz Anna L, Sanders Allison M, Oldenburg Mary C, Koelbl James A, de Arruda-Indig Monika, Halsey Jennifer L, Day Stephen P, Domanico Michael |
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Common susceptibility alleles are unlikely to contribute as strongly as the FV and ABO loci to VTE risk: results from a GWAS approach.
Blood 2009 May 113 (21): 5298-303. Trégouët David-Alexandre, Heath Simon, Saut Noémie, Biron-Andreani Christine, Schved Jean-François, Pernod Gilles, Galan Pilar, Drouet Ludovic, Zelenika Diana, Juhan-Vague Irène, Alessi Marie-Christine, Tiret Laurence, Lathrop Mark, Emmerich Joseph, Morange Pierre-Emmanu |
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ABO genotype and risk of thrombotic events and hemorrhagic stroke.
Journal of thrombosis and haemostasis : JTH 2009 Feb 7 (2): 263-9. Wiggins K L, Smith N L, Glazer N L, Rosendaal F R, Heckbert S R, Psaty B M, Rice K M, Lumley |
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AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
Haematologica 2008 May 93 (5): 729-34. Miñano Antonia, Ordóñez Adriana, España Francisco, González-Porras José Ramón, Lecumberri Ramón, Fontcuberta Jordi, Llamas Pilar, Marín Francisco, Estellés Amparo, Alberca Ignacio, Vicente Vicente, Corral Javi |
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The GOAL study: a prospective examination of the impact of factor V Leiden and ABO(H) blood groups on haemorrhagic and thrombotic pregnancy outcomes.
British journal of haematology 2008 Jan 140 (2): 236-40. Clark Peter, Walker Isobel D, Govan Lindsay, Wu Olivia, Greer Ian |
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A sequence variation scan of the coagulation factor VIII (FVIII) structural gene and associations with plasma FVIII activity levels.
Blood 2007 May 109 (9): 3713-24. Viel Kevin R, Machiah Deepa K, Warren Diane M, Khachidze Manana, Buil Alfonso, Fernstrom Karl, Souto Juan C, Peralta Juan M, Smith Todd, Blangero John, Porter Sandra, Warren Stephen T, Fontcuberta Jordi, Soria Jose M, Flanders W Dana, Almasy Laura, Howard Tom |
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ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens.
Thrombosis and haemostasis 2007 Apr 97 (4): 534-41. Morelli Vania M, de Visser Marieke C H, van Tilburg Nico H, Vos Hans L, Eikenboom Jeroen C J, Rosendaal Frits R, Bertina Rogier |
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Low-density lipoprotein receptor-related protein 1 polymorphism 663 C > T affects clotting factor VIII activity and increases the risk of venous thromboembolism.
Journal of thrombosis and haemostasis : JTH 2007 Mar 5 (3): 497-502. Vormittag R, Bencur P, Ay C, Tengler T, Vukovich T, Quehenberger P, Mannhalter C, Pabinger |
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ABO blood group but not haemostasis genetic polymorphisms significantly influence thrombotic risk: a study of 180 homozygotes for the Factor V Leiden mutation.
British journal of haematology 2006 Dec 135 (5): 697-702. Authors are not available |
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Contribution of low density lipoprotein receptor-related protein genotypes to coagulation factor VIII levels in thrombotic women.
Haematologica 2006 Sep 91 (9): 1261-3. Marchetti Giovanna, Lunghi Barbara, Legnani Cristina, Cini Michela, Pinotti Mirko, Mascoli Francesco, Bernard Frances |
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The ABO blood group genotype and factor VIII levels as independent risk factors for venous thromboembolism.
Thrombosis and haemostasis 2005 Mar 93 (3): 468-74. Tirado Isabel, Mateo José, Soria José Manuel, Oliver Arturo, Martínez-Sánchez Elisabeth, Vallvé Cristina, Borrell Monserrat, Urrutia Teresa, Fontcuberta Jor |
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Relationship between ABO and Secretor genotype with plasma levels of factor VIII and von Willebrand factor in thrombosis patients and control individuals.
British journal of haematology 2005 Jan 128 (1): 100-7. Schleef Michael, Strobel Erwin, Dick Andrea, Frank Josef, Schramm Wolfgang, Spannagl Micha |
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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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