Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Vania Lombardo"'
Autor:
Vania Lombardo, Fania Puccia, Antonino Terranova, Andrea Affronti, Ada Maria Florena, Lydia Giannitrapani, Maurizio Soresi
Publikováno v:
Italian Journal of Medicine, Vol 12, Iss 1, Pp 61-66 (2018)
Hemophagocytic syndrome (HS) is a rare disorder of the immune system. It is characterized by fever, lymphadenopathy, hepatosplenomegaly, cytopenia and hyperferritinemia. The cause differs in each country suggesting a specific genetic background and e
Externí odkaz:
https://doaj.org/article/3ef941d2023b43edb1f292378ad8ea3e
Autor:
Lydia Giannitrapani, Piero Luigi Almasio, Maria Giovanna Minissale, Giuseppe Montalto, Ilaria Morreale, Maurizio Soresi, Vania Lombardo, Fania Puccia, Antonietta Serruto, Anna Licata
Publikováno v:
European Journal of Gastroenterology & Hepatology. 30:226-232
Aim/Objective/Background Direct-acting oral anticoagulant drugs are marketed worldwide for the primary and secondary prevention and treatment of thromboembolic disorders. Rivaroxaban, an oral, direct factor Xa inhibitor, is one of the most used. Riva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::208fa6ab4c0e8636756fa1e2157f1609
https://doi.org/10.1097/meg.0000000000001030
https://doi.org/10.1097/meg.0000000000001030
Autor:
Lydia Giannitrapani, Maurizio Soresi, Vania Lombardo, Anna Licata, Giovanni Mazzola, Fania Puccia
Cytomegalovirus (CMV) infection is usually asymptomatic and self-limiting in healthy individuals, but significant complications can develop in immunosuppressed patients. Venous or arterial thromboembolic phenomena are uncommon yet very serious compli
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f99cbf757b1535cecb32d5c0961e1ba0
http://hdl.handle.net/10447/236540
http://hdl.handle.net/10447/236540
Autor:
Maurizio Soresi, Antonino Terranova, Ada Maria Florena, Lydia Giannitrapani, Vania Lombardo, Fania Puccia, Andrea Affronti
Publikováno v:
Italian Journal of Medicine, Vol 12, Iss 1, Pp 61-66 (2018)
Hemophagocytic syndrome (HS) is a rare disorder of the immune system. It is characterized by fever, lymphadenopathy, hepatosplenomegaly, cytopenia and hyperferritinemia. The cause differs in each country suggesting a specific genetic background and e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55f3d5af364e93e34162d5dd823d1b0d
https://doi.org/10.4081/itjm.2018.932
https://doi.org/10.4081/itjm.2018.932