Journal of Thrombosis and Haemostasis

Novel roles of cAMP/cGMP-dependent signaling in platelets
pp. 167-176(10)
Author: SMOLENSKI, A.

Megakaryocytes, malignancy and bone marrow vascular niches
pp. 177-188(12)
Authors: PSAILA, B.; LYDEN, D.; ROBERTS, I.

Comparison of associations of adherence to a Dietary Approaches to Stop Hypertension (DASH)-style diet with risks of cardiovascular disease and venous thromboembolism
pp. 189-198(10)
Authors: FITZGERALD, K. C.; CHIUVE, S. E.; BURING, J. E.; RIDKER, P. M.; GLYNN, R. J.

The gain-of-function variant allele CYP2C19*17: a double-edged sword between thrombosis and bleeding in clopidogrel-treated patients
pp. 199-206(8)
Authors: LI, Y.; TANG, H.-L.; HU, Y.-F.; XIE, H.-G.

High sCD40L levels early after trauma are associated with enhanced shock, sympathoadrenal activation, tissue and endothelial damage, coagulopathy and mortality
pp. 207-216(10)
Authors: JOHANSSON, P. I.; SØRENSEN, A. M.; PERNER, A.; WELLING, K.-L.; WANSCHER, M.; LARSEN, C. F.; OSTROWSKI, S. R.

Mortality and inherited thrombophilia: results from the European Prospective Cohort on Thrombophilia
pp. 217-222(6)
Authors: PABINGER, I.; VOSSEN, C. Y.; LANG, J.; CONARD, J.; GARCÍA-DABRIO, M. C.; MIESBACH, W.; LEGNANI, C.; SVENSSON, P.; KAIDER, A.; ROSENDAAL, F. R.

Risk of obstetric and thromboembolic complications in family members of women with previous adverse obstetric outcomes carrying common inherited thombophilias
pp. 223-228(6)
Authors: VILLANI, M.; TISCIA, G. L.; MARGAGLIONE, M.; COLAIZZO, D.; FISCHETTI, L.; VERGURA, P.; GRANDONE, E.

Randomized controlled trial of a new portable calf compression device (Venowave) for prevention of venous thrombosis in high-risk neurosurgical patients
pp. 229-235(7)
Authors: SOBIERAJ-TEAGUE, M.; HIRSH, J.; YIP, G.; GASTALDO, F.; STOKES, T.; SLOANE, D.; O'DONNELL, M. J.; EIKELBOOM, J. W.

A simple reminder system improves venous thromboembolism prophylaxis rates and reduces thrombotic events for hospitalized patients<link href="#fn1"/>
pp. 236-243(8)
Authors: MITCHELL, J. D.; COLLEN, J. F.; PETTEYS, S.; HOLLEY, A. B.

Dynamic APTT parameters: applications in thrombophilia
pp. 244-250(7)
Authors: SØRENSEN, B.; INGERSLEV, J.

Precision and accuracy of point-of-care testing coagulometers used for self-testing and self-management of oral anticoagulation therapy
pp. 251-260(10)
Authors: CHRISTENSEN, T. D.; LARSEN, T. B.

Predictors of major bleeding in peri-procedural anticoagulation management
pp. 261-267(7)
Authors: TAFUR, A. J.; McBANE, R.; WYSOKINSKI, W. E.; LITIN, S.; DANIELS, P.; SLUSSER, J.; HODGE, D.; BECKMAN, M. G.; HEIT, J. A.

A role for adhesion and degranulation-promoting adapter protein in collagen-induced platelet activation mediated via integrin α₂β₁
pp. 268-277(10)
Authors: JARVIS, G. E.; BIHAN, D.; HAMAIA, S.; PUGH, N.; GHEVAERT, C. J. G.; PEARCE, A. C.; HUGHES, C. E.; WATSON, S. P.; WARE, J.; RUDD, C. E.; FARNDALE, R. W.

The platelet-surface thiol isomerase enzyme ERp57 modulates platelet function
pp. 278-288(11)
Authors: HOLBROOK, L.-M.; SASIKUMAR, P.; STANLEY, R. G.; SIMMONDS, A. D.; BICKNELL, A. B.; GIBBINS, J. M.

A mutation in the β₃ cytoplasmic tail causes variant Glanzmann thrombasthenia by abrogating transition of α_IIbβ₃ to an active state
pp. 289-297(9)
Authors: HAUSCHNER, H.; MOR-COHEN, R.; SELIGSOHN, U.; ROSENBERG, N.

Developmental hemostasis: recommendations for laboratories reporting pediatric samples
pp. 298-300(3)
Authors: IGNJATOVIC, V.; KENET, G.; MONAGLE, P.; On behalf of the perinatal and paediatric haemostasis subcommittee of the scientific and standardization committee of the international society on thrombosis and haemostasiscr4,

Are thrombophilia more multifactorial than we thought: report of mosaicism for FII G20210A and novel FII T20061C gene variants
pp. 301-303(3)
Authors: DJORDJEVIC, V.; MITIC, G.; PRUNER, I.; KOVAC, M.; RADOJKOVIC, D.

Artificially depleted plasmas are not necessarily commutable with native patient plasmas for International Sensitivity Index calibration and International Normalized Ratio derivation
pp. 303-305(3)
Author: VAN DEN BESSELAAR, A. M. H. P.

Rapid genetic diagnosis of heritable platelet function disorders with next-generation sequencing: proof-of-principle with Hermansky-Pudlak syndrome
pp. 306-309(4)
Authors: JONES, M. L.; MURDEN, S. L.; BEM, D.; MUNDELL, S. J.; GISSEN, P.; DALY, M. E.; WATSON, S. P.; MUMFORD, A. D.; on behalf of the UK GAPP study groupcr9,

RGS2 deficiency in mice does not affect platelet thrombus formation at sites of vascular injury
pp. 309-311(3)
Authors: BANNO, F.; NOJIRI, T.; MATSUMOTO, S.; KAMIDE, K.; MIYATA, T.

Performance of four clinical decision rules in patients with malignancy and suspected pulmonary embolism
pp. 312-314(3)
Authors: VAN ES, J.; DOUMA, R. A.; MOS, I. C. M.; HUISMAN, M. V.; KAMPHUISEN, P. W.

Identification and characterization of mutations in the promoter region of the factor VIII gene
pp. 314-317(4)
Authors: ZIMMERMANN, M. A.; MEIER, D.; OLDENBURG, J.; MÜLLER, C. R.; ROST, S.

2B or not 2B? Masquerading as von Willebrand disease?
pp. 317-319(3)
Authors: FAVALORO, E. J.; KOUTTS, J.

More on: racial differences in venous thromboembolism
pp. 319-320(2)
Authors: MIYATA, T.; HAMASAKI, N.; WADA, H.; KOJIMA, T.

Novel analysis of clinically relevant diagnostic errors in point-of-care devices: a rebuttal
pp. 321-322(2)
Author: HOLLAND, L.

Novel analysis of clinically relevant diagnostic errors in point-of-care devices: a reply to a rebuttal
pp. 322-323(2)
Authors: SHERMOCK, K. M.; STREIFF, M. B.; PINTO, B. L.; KRAUS, P.; PRONOVOST, P. J.

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pp. 324-325(2)