HuGE Literature Finder
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| Phenotypic and Genotypic Signatures of VWF Exon 18 in Eastern Saudi Patients Previously Diagnosed with Type 1 von Willebrand Disease. International journal of general medicine 2022 6 15 5385-5394. Alzahrani Faisal M, Al Faris Asma A, Bashawri Layla A, Hassan Fathelrahman Mahdi, El-Masry Omar S, Aldossary Maryam A, Al Sultan Osama, Borgio J Francis, Alsahli Mohammed A, Goodeve An |
| Unraveling the Influence of Common von Willebrand factor variants on von Willebrand Disease Phenotype: An Exploratory Study on the Molecular and Clinical Profile of von Willebrand Disease in Spain Cohort. Thrombosis and haemostasis 2020 Mar 120 (3): 437-448. Borràs Nina, Garcia-Martínez Iris, Batlle Javier, Pérez-Rodríguez Almudena, Parra Rafael, Altisent Carme, López-Fernández María Fernanda, Costa Pinto Joana, Batlle-López Fernando, Cid Ana Rosa, Bonanad Santiago, Cabrera Noelia, Moret Andrés, Mingot-Castellano María Eva, Navarro Nira, Pérez-Montes Rocío, Marcellini Shally, Moreto Ana, Herrero Sonia, Soto Inmaculada, Fernández-Mosteirín Núria, Jiménez-Yuste Víctor, Alonso Nieves, de Andrés-Jacob Aurora, Fontanes Emilia, Campos Rosa, Paloma María José, Bermejo Nuria, Berrueco Rubén, Mateo José, Arribalzaga Karmele, Marco Pascual, Palomo Ángeles, Castro Quismondo Nerea, Iñigo Belén, Del Mar Nieto María, Vidal Rosa, Martínez María Paz, Aguinaco Reyes, Tenorio Maria, Ferreiro María, García-Frade Javier, Rodríguez-Huerta Ana María, Cuesta Jorge, Rodríguez-González Ramón, García-Candel Faustino, Dobón Manuela, Aguilar Carlos, Corrales Irene, Vidal Francis |
| Common and Rare Variants in Genes Associated with von Willebrand Factor Level Variation: No Accumulation of Rare Variants in Swedish von Willebrand Disease Patients. TH open : companion journal to thrombosis and haemostasis 2020 11 4 (4): e322-e331. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
| Genetic Variation in the von Willebrand Factor Gene in Swedish von Willebrand Disease Patients. TH open : companion journal to thrombosis and haemostasis 2019 6 2 (1): e39-e48. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
| Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients. Thrombosis and haemostasis 2018 Jul . Lind-Halldén Christina, Manderstedt Eric, Carlberg Daniel, Lethagen Stefan, Halldén Christ |
| Common VWF sequence variants associated with higher VWF and FVIII are less frequent in subjects diagnosed with type 1 VWD. Research and practice in thrombosis and haemostasis 2018 Apr 2 (2): 390-398. Flood Veronica H, Johnsen Jill M, Kochelek Caroline, Slobodianuk Tricia L, Christopherson Pamela A, Haberichter Sandra L, Udani Rupa, Bellissimo Daniel B, Friedman Kenneth D, Montgomery Robert |
| Genetic variation in the C-type lectin receptor CLEC4M in type 1 von Willebrand Disease patients. PloS one 2018 13 (2): e0192024. Manderstedt Eric, Lind-Halldén Christina, Lethagen Stefan, Halldén Christ |
Genome-wide association studies identify genetic loci for low von Willebrand factor levels.
European journal of human genetics : EJHG 2015 Oct . van Loon Janine, Dehghan Abbas, Weihong Tang, Trompet Stella, McArdle Wendy L, Asselbergs Folkert F W, Chen Ming-Huei, Lopez Lorna M, Huffman Jennifer E, Leebeek Frank W G, Basu Saonli, Stott David J, Rumley Ann, Gansevoort Ron T, Davies Gail, Wilson James J F, Witteman Jacqueline C M, Cao Xiting, de Craen Anton J M, Bakker Stephan J L, Psaty Bruce M, Starr John M, Hofman Albert, Wouter Jukema J, Deary Ian J, Hayward Caroline, van der Harst Pim, Lowe Gordon D O, Folsom Aaron R, Strachan David P, Smith Nicolas, de Maat Moniek P M, O'Donnell Christoph |
| 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, |
| Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes. Thrombosis and haemostasis 2008 Jun 99 (6): 1013-8. Lethagen S, Hillarp A, Ekholm C, Mattson E, Halldén C, Friberg B |
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