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                             38 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comprehensive study of antithrombin deficiency in a large cohort of Chinese thrombophilia pedigrees: uncovering 4 SERPINC1 pathogenic variants merely impaired progressive activities Chen, Changming

23 8 p. 2508-2521
artikel
2 “An integrated multitool analysis contributes elements to interpreting unclassified factor IX missense variants associated with hemophilia B”: comment from Lee et al. Lee, Kyumin

23 8 p. 2688-2690
artikel
3 “An integrated multitool analysis contributes elements to interpreting unclassified factor IX missense variants associated with hemophilia B”: reply Branchini, Alessio

23 8 p. 2691-2693
artikel
4 Annoucements
23 8 p. 2694-2695
artikel
5 A novel genomic approach to elucidate the cause and clinical implications of reduced von Willebrand factor levels Atiq, Ferdows

23 8 p. 2406-2409
artikel
6 Basic regions of factor V and tissue factor pathway inhibitor mediate heavy chain and acidic region interactions on factor V revealed by tethered chemical cleavage Ayombil, Francis

23 8 p. 2449-2460
artikel
7 Benefits of anticoagulation prophylaxis in children undergoing kidney transplant: systematic review and meta-analysis Al-Huniti, Ahmad H.

23 8 p. 2568-2583
artikel
8 Chromogenic vs one-stage assay to diagnose women and girls with hemophilia A—mapping global approaches and assessing challenges: communication from the SSCs of the ISTH Srivaths, Lakshmi

23 8 p. 2656-2662
artikel
9 Deciphering conundrums on heparins and circulating histones: hype or hope? Ligi, Daniela

23 8 p. 2393-2395
artikel
10 Different D-dimer assays with age-adjusted cutoffs to exclude pulmonary embolism: secondary analysis of ADJUST-PE study Robert–Ebadi, Helia

23 8 p. 2531-2539
artikel
11 Elevated levels of (active) von Willebrand factor during anticoagulation are associated with early recurrence of venous thromboembolism Poolen, Geke C.

23 8 p. 2558-2567
artikel
12 Expansion microscopy allows quantitative characterization of structural organization of platelet aggregates Faulkner, Emma L.

23 8 p. 2618-2633
artikel
13 Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleeding Friedman, Rachel K.

23 8 p. 2410-2421
artikel
14 Hidden antithrombin defects: time to change and improve our thrombophilia diagnostic approach Corral, Javier

23 8 p. 2399-2402
artikel
15 Implementation and clinical utility of multigene panels for bleeding, platelet, and thrombotic disorders Ramanan, Radha

23 8 p. 2371-2387
artikel
16 Incidence and time trends of pregnancy-related first-time venous thromboembolism: a 33-year Swedish birth registry study Philipson, Jacob

23 8 p. 2473-2482
artikel
17 “Intensive factor VIII (FVIII) replacement in hemophilia patients with hypertrophic synovium: a randomized study”: comment Liu, DanYang

23 8 p. 2684-2685
artikel
18 “Intensive factor VIII replacement in hemophilia patients with hypertrophic synovium: a randomized study”: reply Di Minno, Matteo Nicola Dario

23 8 p. 2686-2687
artikel
19 Issue Information
23 8 p. e1-e5
artikel
20 Lack of overt bleeding or platelet dysfunction in a mouse model of vascular Ehlers–Danlos syndrome Lee, Robert H.

23 8 p. 2680-2683
artikel
21 Length of ischemia duration is associated with fibrin film coverage of acute myocardial infarction thrombi Ariëns, Robert A.S.

23 8 p. 2540-2549
artikel
22 Mortality, diagnosis, and etiology of disseminated intravascular coagulation—a systematic review and meta-analysis: communication from the ISTH SSC subcommittee on disseminated intravascular coagulation Umemura, Yutaka

23 8 p. 2663-2679
artikel
23 Multicenter study to improve clinical interpretation of anticardiolipin and anti-β2-glycoprotein I antibody test results for diagnosis of antiphospholipid syndrome Van Hoovels, Lieve

23 8 p. 2584-2597
artikel
24 Outcomes of immune tolerance induction with rituximab to eradicate high-titer inhibitor of hemophilia A: depicted by exponential decay model and the gene expression profile of different outcomes by RNA-sequencing Li, Zekun

23 8 p. 2436-2448
artikel
25 Pathways regulating the levels of tissue factor–positive extracellular vesicles and activation of coagulation in endotoxemic mice Sachetto, Ana T.A.

23 8 p. 2422-2435
artikel
26 Plasma peptidomics: cutting coagulation down to size Brake, Marisa A.

23 8 p. 2396-2398
artikel
27 Poor self-rated health is common in venous thromboembolism: an underestimated health issue Jara–Palomares, Luis

23 8 p. 2403-2405
artikel
28 Prostacyclin enlists AC6 to stop the clot Martin, Kathleen

23 8 p. 2390-2392
artikel
29 Proteolytic neutralization of extracellular histones by neutrophil elastase is enhanced by heparin Huckriede, Joram

23 8 p. 2483-2493
artikel
30 Proteolytic signatures of coagulation identified by plasma peptidomics Del Castillo Alferez, Jessica

23 8 p. 2494-2507
artikel
31 Recombinant a disintegrin-like and metalloproteinase with thrombospondin type 1 motifs 13 (ADAMTS-13) for acute and prophylactic treatment of congenital thrombotic thrombocytopenic purpura in pregnancy Avnon, Taeer

23 8 p. 2598-2603
artikel
32 Self-rated health in venous thromboembolism survivors: a prevalence study Viuff, Jakob Hansen

23 8 p. 2522-2530
artikel
33 Successful use of aflibercept for high cardiac output in hereditary hemorrhagic telangiectasia after failure of pazopanib and bevacizumab therapy Mathavan, Akshay

23 8 p. 2651-2655
artikel
34 The critical role of platelet adenylyl cyclase 6 in hemostasis and thrombosis Webb, Beth A.

23 8 p. 2604-2617
artikel
35 The factor (F)VIII K1693N mutation (FVIII-Nara) in a patient with moderate hemophilia A confers resistance to thrombin-catalyzed cleavage at Arg1689 involving P4ʹ position Furukawa, Shoko

23 8 p. 2461-2472
artikel
36 Venous thromboembolism after hospitalization for COVID-19: venous thrombosis virtual surveillance in COVID study Siegal, Deborah M.

23 8 p. 2550-2557
artikel
37 Venous thromboembolism in pregnancy: more prevention is needed Sørensen, Henrik Toft

23 8 p. 2388-2389
artikel
38 von Willebrand disease-specific defects and proteomic signatures in endothelial colony–forming cells Laan, Sebastiaan N.J.

23 8 p. 2634-2650
artikel
                             38 gevonden resultaten
 
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