Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Granzotto M"'
Autor:
Claudio Tripodo, Marilena Granzotto, Sara Capolla, Gabriele Pozzato, Ruben Spretz, Michele Dal Bo, Luis Nunez, Sonia Zorzet, Paolo Macor, Gustavo Larsen, Sandra Noriega, Nelly Mezzaroba, Eduardo Mansilla, Francesca Vita, Ramiro Mendoza-Maldonado, Valter Gattei
Publikováno v:
Nano Research. 9:537-548
Current approaches for the treatment of chronic lymphocytic leukemia (CLL) have greatly improved the prognosis for survival, but some patients remain refractive to these therapeutic regimens. Hence, in addition to reducing the long-term sideeffects o
Merkel Cell polyomavirus (MCPyV), a ubiquitous DNA tumor virus, has been found to be associated with Merkel cell carcinoma and chronic lymphocytic leukaemia while other associations are still being explored. MCPyV sequences have also been detected in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::beab0bb517de307989070f33452e2dfb
https://hdl.handle.net/11368/2692215
https://hdl.handle.net/11368/2692215
Autor:
Sabina Passamonti, Federica Tramer, Luigi Candussio, Jovana Cvorovic, Marilena Granzotto, Giuliana Decorti
Colorectal cancer is the second most frequent cause of cancer death in the western world. Although the prognosis has improved after the introduction of newer anticancer drugs, the treatment of metastatic colorectal cancer still remains a challenge du
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb89113f0324986576b8c7e8f629fde6
http://hdl.handle.net/11368/2497756
http://hdl.handle.net/11368/2497756
Autor:
Andrea D'Osualdo, Alessandro Ventura, Sergio Crovella, Hans R. Waterham, Lorenzo Calligaris, Marco Nevyjel, Alessandra Pontillo, Alberto Tommasini, Egidio Barbi, Marilena Granzotto
Publikováno v:
Pediatrics, 119(2), e523-e527. American Academy of Pediatrics
Mevalonate kinase deficiency is a rare inborn disorder of isoprenoid and sterol biosynthesis characterized by a recurrent autoinflammatory syndrome and, in most severe cases, psychomotor delay. Clinical manifestations can be very complex and, in some
Autor:
Egidio Barbi, Alberto Tommasini, Andrea Taddio, Erica Valencic, Alessandro Ventura, M. Andolina, Marilena Granzotto, Elena Faleschini, Loredana Lepore
This work studies IPEX (Immunodysregulation with Polyendocrinopathy and Enteropathy X-linked), a severe disorder of course in early childhood due to mutations in the FOXP3 gene (locus Xp11.23-q13.3) leading to failure in immune tolerance and his ther
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aaf93436405d1828099141427433efd6
https://hdl.handle.net/11368/1702669
https://hdl.handle.net/11368/1702669
Autor:
Francesca Gombac, Marlenka Zerial, Valentina Leone, Alberto Tommasini, Loredana Lepore, Alessandro Ventura, Roberta Ciambra, Marilena Granzotto
Publikováno v:
Pediatric hematology and oncology. 22(2)
Chronic granulomatous disease (CGD) is a rare genetically determined immunodeficiency. Neutrophils from CGD patients show a defective killing of phagocytosed fungi and bacteria, due not only to an impairment in oxidative burst, but also to absence of
Autor:
Chiara Garrovo, Gustavo Horacio Marín, Marilena Granzotto, Gabriele Baj, Sonia Zorzet, Luis Nunez, Stefania Biffi, Nelly Mezzaroba, Ruben Spretz, Sandra Noriega, Marianna Lucafò, Eduardo Mansilla, Erika Secco, Gustavo Larsen, Valter Gattei, Marco Calvaruso, Ramiro Mendoza-Maldonado, Sara Capolla, Gabriele Pozzato, Claudio Tripodo, Paolo Macor
Publikováno v:
PLoS ONE, Vol 8, Iss 9, p e74216 (2013)
PLoS ONE
PLoS ONE
Current B-cell disorder treatments take advantage of dose-intensive chemotherapy regimens and immunotherapy via use of monoclonal antibodies. Unfortunately, they may lead to insufficient tumor distribution of therapeutic agents, and often cause adver