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Immunochip analysis identifies novel susceptibility loci in the human leukocyte antigen region for acquired thrombotic thrombocytopenic purpura.
Mancini I, Ricaño-Ponce I, Pappalardo E, Cairo A, Gorski MM, Casoli G, Ferrari B, Alberti M, Mikovic D, Noris M, Wijmenga C, Peyvandi F; Italian Group of TTP Investigators. Mancini I, et al. Among authors: cairo a. J Thromb Haemost. 2016 Dec;14(12):2356-2367. doi: 10.1111/jth.13548. Epub 2016 Dec 3. J Thromb Haemost. 2016. PMID: 27762046 Free article.
Novel aspects of factor XIII deficiency.
Muszbek L, Bagoly Z, Cairo A, Peyvandi F. Muszbek L, et al. Among authors: cairo a. Curr Opin Hematol. 2011 Sep;18(5):366-72. doi: 10.1097/MOH.0b013e3283497e3e. Curr Opin Hematol. 2011. PMID: 21738029 Review.
Classification of rare bleeding disorders (RBDs) based on the association between coagulant factor activity and clinical bleeding severity.
Peyvandi F, Di Michele D, Bolton-Maggs PH, Lee CA, Tripodi A, Srivastava A; Project on Consensus Definitions in Rare Bleeeding Disorders of the Factor VIII/Factor IX Scientific and Standardisation Committee of the International Society on Thrombosis and Haemostasis. Peyvandi F, et al. J Thromb Haemost. 2012 Sep;10(9):1938-43. doi: 10.1111/j.1538-7836.2012.04844.x. J Thromb Haemost. 2012. PMID: 22943259 Free article. No abstract available.
The D173G mutation in ADAMTS-13 causes a severe form of congenital thrombotic thrombocytopenic purpura. A clinical, biochemical and in silico study.
Lancellotti S, Peyvandi F, Pagliari MT, Cairo A, Abdel-Azeim S, Chermak E, Lazzareschi I, Mastrangelo S, Cavallo L, Oliva R, De Cristofaro R. Lancellotti S, et al. Among authors: cairo a. Thromb Haemost. 2016 Jan;115(1):51-62. doi: 10.1160/TH15-02-0119. Epub 2015 Aug 13. Thromb Haemost. 2016. PMID: 26272487
77 results