المؤلفون: 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., Lordkipanidze M.

المساهمون: P. Gresele, E. Falcinelli, L. Bury, A. Pecci, M.-. Alessi, M. Borhany, P.G. Heller, C. Santoro, A.R. Cid, S. Orsini, P. Fontana, E. De Candia, G. Podda, M. Kannan, K. Jurk, G. Castaman, C. Falaise, G. Guglielmini, P. Nori, C. Zaninetti, M. Fiore, A. Tosetto, P. Zuniga, K. Miyazaki, A. Dupui, C. Hayward, A. Casonato, E. Grandone, M.G. Mazzucconi, P. Jame, F. Fabri, Y. Hensken, M. Napolitano, J. Curnow, V. Gkalea, M. Fedor, M.P. Lambert, B. Zieger, L. Barcella, B. Cosmi, P. Giordano, C. Porri, F. Melazzini, M. Abid, A.C. Glembotsky, G. Ferrara, A. Russo, H. Deckmyn, A.L. Frelinger, P. Harrison, D. Mezzano, A.D. Mumford, M. Lordkipanidze

مصطلحات موضوعية: bleeding prediction, bleeding score, inherited platelet disorder, mild-moderate bleeding disorder, von Willebrand disease, Child, Communication, Hemorrhage, Human, Platelet Function Test, von Willebrand Factor, Blood Platelet Disorder, von Willebrand Diseases, Settore MED/09 - Medicina Interna

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33880867; info:eu-repo/semantics/altIdentifier/wos/WOS:000641553500025; volume:19; issue:5; firstpage:1364; lastpage:1371; numberofpages:8; journal:JOURNAL OF THROMBOSIS AND HAEMOSTASIS; http://hdl.handle.net/2434/877010Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85106700271

الإتاحة: https://doi.org/10.1111/jth.15263Test
http://hdl.handle.net/2434/877010Test

المؤلفون: 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

المساهمون: Università degli Studi di Perugia = University of Perugia (UNIPG), Centre recherche en CardioVasculaire et Nutrition = Center for CardioVascular and Nutrition research (C2VN), Aix Marseille Université (AMU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Institut National de Recherche pour l’Agriculture, l’Alimentation et l’Environnement (INRAE), Unidad de Coagulopatías Congénitas. Hospital Universitario La Fe., Gresele, Paolo, Falcinelli, Emanuela, Bury, Loredana, Pecci, Alessandro, Alessi, Marie-Christine, Borhany, Munira, Heller, Paula G, Santoro, Cristina, Cid, Ana Rosa, Orsini, Sara, Fontana, Pierre, De Candia, Erica, Podda, Gianmarco, Kannan, Meganathan, Jurk, Kerstin, Castaman, Giancarlo, Falaise, Céline, Guglielmini, Giuseppe, Noris, Patrizia, Mariasanta Napolitano, Università degli Studi di Perugia (UNIPG), University of Perugia, 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

المصدر: 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

مصطلحات موضوعية: medicine.medical_specialty, animal structures, mild‐, Platelet Function Tests, Platelet disorder, inherited platelet disorder, Hemorrhage, 030204 cardiovascular system & hematology, Hemorrhage/diagnosis, 03 medical and health sciences, 0302 clinical medicine, Von Willebrand factor, hemic and lymphatic diseases, Internal medicine, von Willebrand Factor, Von Willebrand disease, Medicine, Humans, Platelet, Bleeding prediction, Bleeding score, Blood platelet disorders, Child, Communication, Hemorrhage, Humans, Inherited platelet disorders, Mild-moderate bleeding disorders, Platelet Function Tests, von Willebrand diseases, von Willebrand Factor, Child, Blood Platelet Disorders, ddc:616, mild-moderate bleeding disorders, biology, business.industry, mild-moderate bleeding disorder, Incidence (epidemiology), Communication, Settore MED/09 - MEDICINA INTERNA, bleeding prediction, von Willebrand Diseases/diagnosis/genetics, [SDV.MHEP.HEM]Life Sciences [q-bio]/Human health and pathology/Hematology, Hematology, medicine.disease, Blood Platelet Disorders/diagnosis/genetics, 3. Good health, bleeding score, Institutional repository, von Willebrand Diseases, moderate bleeding disorders, inherited platelet disorders, Quartile, biology.protein, von Willebrand disease, business

وصف الملف: STAMPA

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::92e5881224dd6b78cdce3a0c34718e47Test
https://pubmed.ncbi.nlm.nih.gov/33880867Test

المؤلفون: De Candia E.

المساهمون: 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, Erica, Podda, G., Kannan, M., Jurk, K., Castaman, G., Falaise, C., Guglielmini, G., Noris, P.

مصطلحات موضوعية: bleeding prediction, bleeding score, inherited platelet disorders, mild-moderate bleeding disorders, von Willebrand disease, Child, Communication, Hemorrhage, Humans, Platelet Function Tests, von Willebrand Factor, Blood Platelet Disorders, von Willebrand Diseases, Settore MED/09 - MEDICINA INTERNA

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/33880867; info:eu-repo/semantics/altIdentifier/wos/WOS:000641553500025; volume:19; issue:5; firstpage:1364; lastpage:1371; numberofpages:8; issueyear:2021; journal:JOURNAL OF THROMBOSIS AND HAEMOSTASIS; http://hdl.handle.net/10807/183023Test; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85106700271

الإتاحة: https://doi.org/10.1111/jth.15263Test
http://hdl.handle.net/10807/183023Test