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British Journal of Haematology|February 27, 2015
Are all cases of paediatric essential thrombocythaemia really myeloproliferative neoplasms? Analysis of a large cohortMaria L Randi, Giulia Geranio, Irene Bertozzi, et al.
Blood|July 4, 2014
Platelet diameters in inherited thrombocytopenias: analysis of 376 patients with all known disordersPatrizia Noris, Ginevra Biino, Alessandro Pecci, et al.
Human Mutation|December 7, 2007
Position of nonmuscle myosin heavy chain IIA (NMMHC-IIA) mutations predicts the natural history of MYH9-related diseaseAlessandro Pecci, Emanuele Panza, Núria Pujol-Moix, et al.
Haematologica|September 28, 2019
Antithrombotic prophylaxis for surgery-associated venous thromboembolism risk in patients with inherited platelet disorders. The SPATA-DVT StudyFrancesco Paciullo, Loredana Bury, Patrizia Noris, et al.
Haematologica|April 8, 2017
Bleeding risk of surgery and its prevention in patients with inherited platelet disordersSara Orsini, Patrizia Noris, Loredana Bury, et al.
Human Mutation|June 18, 2014
Spectrum of the mutations in Bernard-Soulier syndromeAnna Savoia, Shinji Kunishima, Daniela De Rocco, et al.
Human Mutation|November 5, 2013
MYH9-related disease: a novel prognostic model to predict the clinical evolution of the disease based on genotype-phenotype correlationsAlessandro Pecci, Catherine Klersy, Paolo Gresele, et al.
Haematologica|April 26, 2014
Analysis of 339 pregnancies in 181 women with 13 different forms of inherited thrombocytopeniaPatrizia Noris, Nicole Schlegel, Catherine Klersy, et al.
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