Items where authors include "Castaman, G."

Article

Wheeler, A.P. orcid.org/0000-0003-3967-4873, Abraham, A., Barnes, C. et al. (12 more authors) (2025) Real‐world unmet needs of patients with haemophilia A and haemophilia B with or without inhibitors: End‐of‐study results from the explorer6 non‐interventional study. Haemophilia, 31 (5). pp. 903-911. ISSN 1351-8216

Rodeghiero, F. orcid.org/0000-0003-2253-2502, Ghiotto, L. orcid.org/0009-0008-6438-7810, Pontalto, L. et al. (23 more authors) (2025) Mild or moderate hemophilia is not always a mild or moderate bleeding disorder: back to the clinical phenotype. HemaSphere, 9 (3). e70111. ISSN 2572-9241

Pagliari, M.T., Rosendaal, F.R., Ahmadinejad, M. et al. (29 more authors) (2022) Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study. Journal of Thrombosis and Haemostasis, 20 (5). pp. 1106-1114. ISSN 1538-7933

Tosetto, A., Badiee, Z., Baghaipour, M. et al. (32 more authors) (2020) Bleeding symptoms in patients diagnosed as type 3 von willebrand disease: results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study. Journal of Thrombosis and Haemostasis, 18 (9). pp. 2145-2154. ISSN 1538-7933

Makris, M. orcid.org/0000-0001-7622-7939, Oldenburg, J., Mauser-Bunschoten, E.P. et al. (4 more authors) (2018) The definition, diagnosis and management of mild hemophilia A: communication from the SSC of the ISTH. Journal of Thrombosis and Haemostasis, 16 (12). pp. 2530-2533. ISSN 1538-7933

Iorio, A., Barbara, A., Makris, M. orcid.org/0000-0001-7622-7939 et al. (21 more authors) (2017) Natural history and clinical characteristics of inhibitors in previously treated haemophilia A patients: A case series. Haemophilia, 23 (2). pp. 255-263. ISSN 1351-8216

Castaman, G., Hillarp, A. and Goodeve, A. orcid.org/0000-0002-6177-7062 (2014) Laboratory aspects of von Willebrand disease: test repertoire and options for activity assays and genetic analysis. Haemophilia , 20 (S4). pp. 65-70. ISSN 1351-8216

Hickson, N., Hampshire, D. orcid.org/0000-0002-1387-8926, Castaman, G. et al. (5 more authors) (2011) Effect of the VWF promoter (GT)n repeat and single-nucleotide polymorphism c.-2527G>A on circulating von Willebrand factor levels under normal conditions. Journal of Thrombosis and Haemostasis, 9 (3). pp. 603-605. ISSN 1538-7933

Hickson, N., Hampshire, D. orcid.org/0000-0002-1387-8926, Winship, P. et al. (11 more authors) (2010) von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels. Journal Of Thrombosis And Haemostasis, 8 (9). pp. 1986-1993. ISSN 1538-7933