Reduced survival of type 2B von Willebrand factor, irrespective of large multimer representation or thrombocytopeniaCASONATO, Alessandra; GALLINARO, Lisa; GRAZIA CATTINI, Maria et al.Haematologica (Roma). 2010, Vol 95, Num 8, pp 1366-1372, issn 0390-6078, 7 p.Article

Platelet-Type Von Willebrand Disease: A Rare, Often Misdiagnosed and Underdiagnosed Bleeding DisorderOTHMAN, Maha.Seminars in thrombosis and hemostasis. 2011, Vol 37, Num 5, pp 464-469, issn 0094-6176, 6 p.Article

Platelet-Type von Willebrand Disease and Type 2B von Willebrand Disease : A Story of Nonidentical Twins when Two Different Genetic Abnormalities Evolve into Similar PhenotypesOTHMAN, Maha.Seminars in thrombosis and hemostasis. 2007, Vol 33, Num 8, pp 780-786, issn 0094-6176, 7 p.Article

Phenotypic Identification of Platelet-Type von Willebrand Disease and Its Discrimination from Type 2B von Willebrand Disease : A Question of 2B or Not 2B? A Story of Nonidentical Twins? Or Two Sides of a Multidenominational or Multifaceted Primary-Hemostasis Coin?FAVALORO, Emmanuel J.Seminars in thrombosis and hemostasis. 2008, Vol 34, Num 1, pp 113-127, issn 0094-6176, 15 p.Article

Genetics of type 2B von Willebrand Disease : True 2B, tricky 2B, or Not 2B. What Are the Modifiers of the Phenotype?OTHMAN, Maha; FAVALORO, Emmanuel J.Seminars in thrombosis and hemostasis. 2008, Vol 34, Num 6, pp 520-531, issn 0094-6176, 12 p.Article

A novel D235Y mutation in the GP1BA gene enhances platelet interaction with von Willebrand factor in an Iranian family with platelet-type von Willebrand diseaseENAYAT, Said; RAVANBOD, Shirin; RASSOULZADEGAN, Maryam et al.Thrombosis and haemostasis. 2012, Vol 108, Num 5, pp 952-960, issn 0340-6245, 9 p.Article

A novel von Willebrand factor mutation (11372S) associated with type 2B-like von Willebrand disease : An elusive phenotype and a difficult diagnosisCASONATO, Alessandra; SARTORELLO, Francesca; PONTARA, Elena et al.Thrombosis and haemostasis. 2007, Vol 98, Num 6, pp 1182-1187, issn 0340-6245, 6 p.Article

A first Taiwanese Chinese family of type 2B von Willebrand disease with R1306W mutationSHEN, Ming-Ching; LIN, Jen-Shiou; LIN, David Shih-Yao et al.Thrombosis research. 2003, Vol 112, Num 5-6, pp 291-295, issn 0049-3848, 5 p.Article