Diagnostic challenges of inherited mild bleeding disorders: a bait for poorly explored clinical and basic research

Autor: Mezzano, D. ^*, Quiroga, T.

Publikováno v: In Journal of Thrombosis and Haemostasis February 2019 17(2):257-270

Quantitative impact of using different criteria for the laboratory diagnosis of type 1 von Willebrand disease

Autor: Quiroga, T., Goycoolea, M., Belmont, S., Panes, O., Aranda, E., Zúñiga, P., Pereira, J., Mezzano, D. ^*

Publikováno v: In Journal of Thrombosis and Haemostasis August 2014 12(8):1238-1243

The ISTH bleeding assessment tool as predictor of bleeding events in inherited platelet disorders: Communication from the ISTH SSC Subcommittee on Platelet Physiology

Autor: Gresele, P., Falcinelli, E., Bury, L., Pecci, A., Alessi, M. -C., Borhany, M., Heller, P. G., Santoro, C., Cid, A. R., Orsini, S., Fontana, P., De Candia, E., Podda, G., Kannan, M., Jurk, K., Castaman, G., Falaise, C., Guglielmini, G., Noris, P., Zaninetti, C., Fiore, M., Tosetto, A., Zuniga, P., Miyazaki, K., Dupuis, A., Hayward, C., Casonato, A., Grandone, E., Mazzucconi, M. G., James, P., Fabris, F., Henskens, Y., Napolitano, M., Curnow, J., Gkalea, V., Fedor, M., Lambert, M. P., Zieger, B., Barcella, L., Cosmi, B., Giordano, P., Porri, C., Melazzini, F., Abid, M., Glembotsky, A. C., Ferrara, G., Russo, A., Deckmyn, H., Frelinger, A. L., Harrison, P., Mezzano, D., Mumford, A. D., Lordkipanidzé, M., BAT-VAL Study Investigators

Publikováno v: Journal of Thrombosis and Haemostasis
Journal of Thrombosis and Haemostasis, 2021, 19 (5), pp.1364-1371. ⟨10.1111/jth.15263⟩
Journal of Thrombosis and Haemostasis, Wiley, 2021, 19 (5), pp.1364-1371. ⟨10.1111/jth.15263⟩
Journal of thrombosis and haemostasis : JTH
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
Journal of Thrombosis and Haemostasis, Vol. 19, No 5 (2021) pp. 1364-1371

Background: The ISTH Bleeding Assessment Tool (ISTH-BAT) has been validated for clinical screening of suspected von Willebrand disease (VWD) and for bleeding prediction. Recently it has been validated for subjects with inherited platelet disorders (I

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e5881224dd6b78cdce3a0c34718e47
https://pubmed.ncbi.nlm.nih.gov/33880867

Template bleeding time and PFA‐100® have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: comparative study in 148 patients

Autor: Quiroga, T., Goycoolea, M., Muñoz, B., Morales, M., Aranda, E., Panes, O., Pereira, J., Mezzano, D. ^*

Publikováno v: In Journal of Thrombosis and Haemostasis June 2004 2(6):892-898

Fibrin and D-dimer bind to monomeric GPVI

Autor: Onselaer, M-B, Hardy, AT, Wilson, C, Sanchez, X, Babar, AK, Miller, JLC, Watson, CN, Watson, SK, Bonna, A, Philippou, H, Herr, AB, Mezzano, D, Ariëns, RAS, Watson, SP

Fibrin has recently been shown to activate platelets through the immunoglobulin receptor glycoprotein VI (GPVI). In the present study, we show that spreading of human platelets on fibrin is abolished in patients deficient in GPVI, confirming that fib

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::43e8b8d9d54b1db32fe2e35e7de86eaf
https://eprints.whiterose.ac.uk/138869/9/1495.full.pdf