Zobrazeno 1 - 10
of 198
pro vyhledávání: '"F. Rodeghiero and"'
Autor:
F. Rodeghiero, V. De Stefano, Cristina Santoro, Sergio Siragusa, Nicola Vianelli, Francesco Zaja, Federico Chiurazzi, Giuseppe Carli, Monica Carpenedo, Valentina Carrai, Silvia Cantoni
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases. 13
The current COVID-19 pandemic requires revisiting our current approach to major blood disorders, including ITP (Immune Thrombocytopenia), stirring up the production of several disease-specific practical guidelines. This report describes an updated ve
Publikováno v:
Journal of thrombosis and haemostasis : JTH. 16(9)
Hereditary thrombocytopenias (HTPs) constitute a heterogeneous group of diseases characterized by a reduction in platelet count and a potential bleeding risk. As a result of advances in diagnostic methods, HTPs are increasingly being identified, and
Autor:
D. Arnold, N. Hashemi Sadraei, F. Rodeghiero, A. Janssens, C. Turkington, D. Selleslag, A. Newland, J. Mayer, R. Bird, D. Kuter
Publikováno v:
HemaSphere. 3:302-303
Autor:
F. Rodeghiero
Publikováno v:
Journal of Thrombosis and Haemostasis. 12:1234-1237
Autor:
F. Valeri, W. Barcellini, Francesco Zaja, Renato Fanin, E. Rossi, F. Palandri, Nicola Vianelli, E. Crea, S. Volpetti, E. Lucchini, I. Giardini, Marco Vignetti, Giuseppe Carli, E. Boggio, Giuseppe Auteri, U. Consoli, Monica Carpenedo, F. Rodeghiero, U. Dianzani, Andrea Patriarca, F. Rotondo, Cristina Santoro
Publikováno v:
HemaSphere. 3:302
Autor:
Alessandra Frattini, Carlo Fumagalli, Ferruccio Trifiro, M. Ricotta, Gianluca Mazzoni, F. Rodeghiero, G. Puccinotti, Fabrizio Cavani, Carlotta Cortelli
Publikováno v:
Topics in Catalysis. 38:295-301
This paper describes the preparation, characterization and reactivity in n-butane oxidation of catalysts made of vanadyl pyrophosphate (VPP) diluted in aluminum phosphate. Catalysts were prepared by synthesizing at the same time the VPP precursor and
Publikováno v:
Journal of Thrombosis and Haemostasis. 11:142-150
Bleeding symptoms are frequently reported even in otherwise healthy subjects, and differentiating a normal subject from a patient with a mild bleeding disorder (MBD) can be extremely challenging. The concept of bleeding rate, that is, the number of b
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 3(3)
Summary. Acquired haemophilia is a rare but often catastrophic haemorrhagic disorder associated with a high mortality rate. No single therapeutic approach has been consistently successful and clinical experience remains mainly anecdotal. This report
Autor:
F. Rodeghiero, Sandra L. Haberichter, U. Budde, Giancarlo Castaman, Reinhard Schneppenheim, Paula M. Jacobi, Tobias Obser, Sofia H. Giacomelli
Publikováno v:
Journal of Thrombosis and Haemostasis. 10:951-958
Summary. Background: von Willebrand disease (VWD) is caused by mutations in von Willebrand factor (VWF) that have different pathophysiologic effect in causing low plasma VWF levels. Type 1 VWD includes quantitative plasma VWF deficiency with normal V
Autor:
F. Elice, F. Rodeghiero
Publikováno v:
Thrombosis Research. 129:360-366
Patients with hematologic malignancies have an increased risk of venous thromboembolism (VTE), particularly at diagnosis and during the treatment with chemotherapy, asparaginase or immunomodulatory drugs (IMiDs). A disease-dependent hypercoagulable c