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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|June 1, 2005
Low frequency of VHL gene mutations in young individuals with polycythemia and high serum erythropoietinMaria Luigia Randi, Alessandra Murgia, Maria Caterina Putti, et al.Platelets|September 16, 2008
A case of Bernard-Soulier Syndrome due to a homozygous four bases deletion (TGAG) of GPIbalpha gene: lack of GPIbalpha but absence of bleedingSilvia Vettore, Raffaella Scandellari, Margherita Scapin, et al.Mediterranean Journal of Hematology and Infectious Diseases|March 12, 2024
Coexistence of Multiple Gene Variants in Some Patients with ErythrocytosesAndrea Benetti, Irene Bertozzi, Giulio Ceolotto, et al.Journal of Clinical Medicine|April 3, 2020
Prevalence and Causes of Anemia in Hospitalized Patients: Impact on Diseases OutcomeMaria Luigia Randi, Irene Bertozzi, Claudia Santarossa, et al.Blood|July 20, 2006
Pediatric patients with essential thrombocythemia are mostly polyclonal and V617FJAK2 negativeMaria Luigia Randi, Maria Caterina Putti, Margherita Scapin, et al.Blood|December 8, 2009
Src tyrosine kinase preactivation is associated with platelet hypersensitivity in essential thrombocythemia and polycythemia veraMaria Luigia Randi, Anna Maria Brunati, Margherita Scapin, et al.Hormones (Athens, Greece)|April 12, 2014
Gonadotropin secreting pituitary adenoma associated with erythrocytosis: case report and literature reviewFilippo Ceccato, Gianluca Occhi, Daniela Regazzo, et al.Pediatric Blood & Cancer|February 27, 2013
MPL W515L mutation in pediatric essential thrombocythemiaPiero Farruggia, Paolo D'Angelo, Maria La Rosa, et al.American Journal of Hematology|October 30, 2013
Masked polycythemia vera diagnosed according to WHO and BCSH classificationTiziano Barbui, Jürgen Thiele, Alessandra Carobbio, et al.Pageof 7