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Aging Clinical and Experimental Research|October 15, 2008
Hydroxyurea in old patients with essential thrombocythemiaMaria Luigia Randi, Elisabetta Ruzzon, Antonio Piccoli, et al.
Medicina (Kaunas, Lithuania)|August 28, 2019
Systemic Mastocytosis and Essential Thrombocythemia: Case Report and Literature OverviewMauro Cancian, Elisabetta Cosi, Marco Pizzi, et al.
The Journal of Organic Chemistry|May 19, 2018
Selective Hydrogenations and Dechlorinations in Water Mediated by Anionic Surfactant-Stabilized Pd NanoparticlesGiorgio La Sorella, Laura Sperni, Patrizia Canton, et al.
Acta Haematologica|February 6, 2010
Heparin-induced thrombocytopenia in patients with Philadelphia-negative myeloproliferative disorders and unusual splanchnic or cerebral vein thrombosisMaria L Randi, Fabiana Tezza, Margherita Scapin, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 18, 2019
Prophylactic protocol for dental care in ligneous gingivitis due to severe plasminogen deficiency: Case report and review of literatureMaria T Sartori, Stefano Sivolella, Irene Di Pasquale, et al.
Internal and Emergency Medicine|March 26, 2021
Admission criteria for a cardiovascular short stay unit: a retrospective analysis on a pilot unitFederico Capone, Leonardo Molinari, Marianna Noale, et al.
Annals of Hematology|June 7, 2017
Thromboses and hemorrhages are common in MPN patients with high JAK2V617F allele burdenIrene Bertozzi, Giulia Bogoni, Giacomo Biagetti, et al.
Haematologica|September 26, 2008
Novel point mutation in a leucine-rich repeat of the GPIbalpha chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variantSilvia Vettore, Raffaella Scandellari, Stefano Moro, et al.
Haematologica|May 15, 2003
Inherited thrombocytopenias: a proposed diagnostic algorithm from the Italian Gruppo di Studio delle PiastrineCarlo L Balduini, Marco Cattaneo, Fabrizio Fabris, et al.
Journal of Thrombosis and Thrombolysis|August 16, 2011
Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes)Antonio Girolami, Girolami Antonio, Silvia Vettore, et al.
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