Search Results - "Santi, Roberto Mario"

Thrombosis in multiple myeloma: risk stratification, antithrombotic prophylaxis, and management of acute events. A consensus-based position paper from an ad hoc expert panel by De Stefano, Valerio, Larocca, Alessandra, Carpenedo, Monica, Cavo, Michele, Di Raimondo, Francesco, Falanga, Anna, Offidani, Massimo, Petrucci, Maria Teresa, Ruggeri, Marco, Santi, Roberto Mario, Barosi, Giovanni

“…The introduction of new therapeutic agents for multiple myeloma (MM), including proteasome inhibitors, immunomodulatory drugs, and monoclonal antibodies, has…”
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Real-World Efficacy and Safety of Plasma-Derived Von Willebrand Factor-Containing Factor VIII Concentrates in Patients With Von Willebrand Disease in Italy by Federici, Augusto B, Santoro, Rita Carlotta, Santoro, Cristina, Pieri, Lisa, Santi, Roberto Mario, Barillari, Giovanni, Borchiellini, Alessandra, Tosetto, Alberto, Zanon, Ezio, De Cristofaro, Raimondo, Mairal, Esther, Mir, Roser

“…Plasma-derived von Willebrand factor-containing factor VIII concentrates (pd-VWF/FVIII-C) are the mainstay of treatment in von Willebrand disease (VWD)…”
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Haemophilic Pelvic Pseudotumour: A New Surgical Option by Pasta, Gianluigi, Ruggieri, Roberta, Annunziata, Salvatore, Gallese, Alessandro, Gagliardi, Vincenzo Pio, Cuzzocrea, Fabrizio, Ghiara, Matteo, Russo, Mariaconcetta, Preti, Paola Stefania, Santi, Roberto Mario, Mosconi, Mario, Benazzo, Francesco

“…Background: Haemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally…”
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Rituximab in lupus anticoagulant hypoprothrombinemia syndrome: A case report by Agnelli Giacchello, Jacopo, Trincheri, Nicol Francesca, Sciancalepore, Patrizia, Contino, Laura, Santi, Roberto Mario, Pengo, Vittorio

“…Background Lupus anticoagulant hypoprothrombinemia syndrome (LAHPS) is a rare autoimmune condition characterized by acquired prothrombin (FII) deficiency…”
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Diagnosis and management of abnormal uterine bleeding in adolescence: An expert Consensus Statement of SIGO (Italian Society of Gynecology and Obstetrics) and SISET (Italian Society for the Study of Hemostasis and Thrombosis) by Santi, Roberto Mario, Fulghesu, Annamaria, Zanon, Ezio, De Candia, Erica, Grandone, Elvira, Di Renzo, Giancarlo, Succu, Claudia, Tosto, Valentina, Bruni, Vincenzina, Gresele, Paolo

“…During menarche and adolescence, abnormal uterine bleeding (AUB) may serve as a crucial indicator of a hidden bleeding disorder. When a young woman is…”
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Diagnosis and management of abnormal uterine bleeding in adolescence by Roberto Mario Santi, Annamaria Fulghesu, Ezio Zanon, Erica De Candia, Elvira Grandone, Giancarlo Di Renzo, Claudia Succu, Valentina Tosto, Vincenzina Bruni, Paolo Gresele

“…During menarche and adolescence, abnormal uterine bleeding (AUB) may serve as a crucial indicator of a hidden bleeding disorder. When a young woman is…”
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Khorana Score and Histotype Predict the Incidence of Early Venous Thromboembolism (VTE) in Non Hodgkin Lymphoma (NHL). a Pooled Data Analysis of Twelve Clinical Trials of Fondazione Italiana Linfomi (FIL) by Santi, Roberto Mario, Ceccarelli, Manuela, Catania, Gioacchino, Monagheddu, Chiara, Evangelista, Andrea, Bernocco, Elisa, Monaco, Federico, Federico, Massimo, Vitolo, Umberto, Cortelazzo, Sergio, Cabras, Maria Giuseppina, Spina, Michele, Baldini, Luca, Boccomini, Carola, Chiappella, Annalisa, Bari, Alessia, Luminari, Stefano, Calabrese, Marco, Levis, Alessandro, Contino, Laura, Ciccone, Giovannino, Ladetto, Marco

“…Background and rationale. Recent studies show that the risk of VTE in NHL pts is similar to that observed in high risk solid tumors (i.e. pancreatic, ovarian…”
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Haemophilic Pelvic Pseudotumour: A New Surgical Option by Pasta, Gianluigi, Ruggieri, Roberta, Annunziata, Salvatore, Gallese, Alessandro, Gagliardi, Vincenzo Pio, Cuzzocrea, Fabrizio, Ghiara, Matteo, Russo, Mariaconcetta, Preti, Paola Stefania, Santi, Roberto Mario, Mosconi, Mario, Benazzo, Francesco

“…BACKGROUNDHaemophilia is an inherited coagulopathy caused by the absence or dysfunction of clotting factor VIII or IX. Clinical manifestations are generally…”
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