Human Genome Epidemiology Literature Finder
Records 1 - 10 (of 10 Records) |
Query Trace: Hemophilia A and VWF[original query] |
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Variation in baseline factor VIII concentration in a retrospective cohort of mild/moderate hemophilia A patients carrying identical F8 mutations. Journal of thrombosis and haemostasis : JTH 2016 Dec . Loomans J I, van Velzen A S, Eckhardt C L, Peters M, Mäkipernaa A, Holmstrom M, Brons P P, Dors N, Haya S, Voorberg J, van der Bom J G, Fijnvandraat |
Genetic determinants of VWF clearance and FVIII binding modify FVIII pharmacokinetics in pediatric hemophilia A patients. Blood 2019 Jul . Swystun Laura L, Ogiwara Kenichi, Rawley Orla, Brown Christine, Georgescu Ilinca, Hopman Wilma, Labarque Veerle, Male Christoph, Thom Katharina, Blanchette Victor S, Carcao Manuel, Lillicrap Dav |
Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A population. Journal of thrombosis and haemostasis : JTH 2020 Nov . Ogiwara Kenichi, Swystun Laura L, Paine A Simonne, Kepa Sylvia, Choi Seon Jai, Rejtö Judit, Hopman Wilma, Pabinger Ingrid, Lillicrap Dav |
The Asialoglycoprotein Receptor Minor Subunit Gene Contributes to Pharmacokinetics of Factor VIII Concentrates in Hemophilia A. Thrombosis and haemostasis 2021 Aug . Lunghi Barbara, Morfini Massimo, Martinelli Nicola, Balestra Dario, Linari Silvia, Frusconi Sabrina, Branchini Alessio, Cervellera Christian F, Marchetti Giovanna, Castaman Giancarlo, Bernardi Frances |
Genetic and Bioinformatic Strategies to Improve Diagnosis in Three Inherited Bleeding Disorders in Bogotá, Colombia. Genes 2021 11 12 (11): . Lago Juliana, Groot Helena, Navas Diego, Lago Paula, Gamboa María, Calderón Dayana, Polanía-Villanueva Diana |
Genetic Alterations, DNA Methylation, Alloantibodies and Phenotypic Heterogeneity in Type III von Willebrand Disease. Genes 2022 6 13 (6): . Naveed Muhammad Asif, Abid Aiysha, Ali Nadir, Hassan Yaqoob, Amar Ali, Javed Aymen, Qamar Khansa, Mustafa Ghulam, Raza Ali, Saleem Umera, Hussain Shabbir, Shakoor Madiha, Khaliq Shagufta, Mohsin Shahi |
Next-generation sequencing of von Willebrand factor and coagulation factor VIII genes: a cross-sectional study in Croatian adult patients diagnosed with von Willebrand disease. Croatian medical journal 2022 5 63 (2): 166-175. Lapi? Ivana, Radi? Antolic Margareta, Boban Ana, Coen Herak Desiree, Rogi? Dunja, Zadro Rena |
The Lesson Learned from the New c.2547-1G?>?T Mutation Combined with p.R854Q: When a Type 2N Mutation Reveals a Quantitative von Willebrand Factor Defect. Thrombosis and haemostasis 2022 2 122 (9): 1479-1485. Casonato Alessandra, Cozzi Maria Rita, Ferrari Silvia, Rubin Beatrice, Gianesello Lisa, De Marco Luigi, Daidone Vivia |
Combination of CLEC4M rs868875 G-Carriership and ABO O Genotypes May Predict Faster Decay of FVIII Infused in Hemophilia A Patients. Journal of clinical medicine 2022 2 11 (3): . Lunghi Barbara, Morfini Massimo, Martinelli Nicola, Linari Silvia, Castaman Giancarlo, Bernardi Frances |
Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor. Journal of thrombosis and haemostasis : JTH 2023 2 . Elsheikh Einas, Lavin Michelle, Heck Lilian Antunes, Larkin Niamh, Mullaney Brendan, Doherty Dearbhla, Kennedy Megan, Keenan Catriona, Guest Thomas, O'Mahony Brian, Fazavana Judicael, Fallon Padraic G, Preston Roger J S, Gormley John, Ryan Kevin, O'Connell Niamh M, Singleton Evelyn, Byrne Mary, McGowan Mark, Roche Sheila, Doyle Mairead, Crowley Maeve P, O'Shea Susan I, Reipert Birgit M, Johnsen Jill M, Pipe Steven W, Di Paola Jorge, Turecek Peter L, O'Donnell James S, |
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