Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Carmen De Fusco"'
Autor:
Francesco Pegoraro, Aurora Chinnici, Linda Beneforti, Michele Tantuli, Irene Trambusti, Carmen De Fusco, Concetta Micalizzi, Alessandra Todesco, Fabiola Dell’acqua, Stefania Gaspari, Maria Luisa Coniglio, Elena Sieni
Publikováno v:
HemaSphere, Vol 7, p e62871f1 (2023)
Externí odkaz:
https://doaj.org/article/67f5d3e0d3f9442fa533351249d9fc2e
Autor:
Francesco Pegoraro, Martina Mazzariol, Irene Trambusti, Saamer Bakhshi, Saumyaranjan Mallick, Ira J. Dunkel, Van den Bos Cor, Ozlem Tezol, Shijun Shan, Suheyla Ocak, Flavio Giordano, Carmen De Fusco, Stefania Gaspari, Jean Donadieu, Eli Diamond, Jean-Francois Emile, Elena Sieni, Julien Haroche, Augusto Vaglio
Publikováno v:
HemaSphere, Vol 7, p e44200f4 (2023)
Externí odkaz:
https://doaj.org/article/239ca57cd85743fabf7d95809c7923ad
Autor:
Alessandra Santoro, Sonia Cannella, Antonino Trizzino, Giuseppa Bruno, Carmen De Fusco, Luigi D. Notarangelo, Daniela Pende, Gillian M. Griffiths, Maurizio Aricò
Publikováno v:
Haematologica, Vol 93, Iss 7 (2008)
Mutations of UNC13D have been described in patients affected by familial hemophagocytic lymphohistiocytosis (FHL3). The Munc13-4 protein contributes to the priming of the secretory granules. Mutation in this gene results in defective cellular cytotox
Externí odkaz:
https://doaj.org/article/ee08ed6387434d7e9a31bfeb6b15aa20
Autor:
Franco Locatelli, Lorenzo Moretta, Concetta Micalizzi, Valentina Cetica, Elena Sieni, Carmen De Fusco, Franca Fagioli, Cesare Danesino, Maria Caterina Putti, Maurizio Aricò, Andrea Biondi, Lucio Luzzatto, Gillian M. Griffiths, Daniela Pende
Publikováno v:
The Journal of Allergy and Clinical Immunology
Background Hemophagocytic lymphohistiocytosis (HLH) is a rare life-threatening disease affecting mostly children but also adults and characterized by hyperinflammatory features. A subset of patients, referred to as having familial hemophagocytic lymp
Autor:
Daniela Pende, Alessandra Santoro, Giuseppa Bruno, Sonia Cannella, Carmen De Fusco, Luigi D. Notarangelo, Antonino Trizzino, Maurizio Aricò, Gillian M. Griffiths
Publikováno v:
Haematologica. 93(7)
Mutations of UNC13D have been described in patients affected by familial hemophagocytic lymphohistiocytosis (FHL3). The Munc13-4 protein contributes to the priming of the secretory granules. Mutation in this gene results in defective cellular cytotox
Autor:
Antonino Trizzino, Alessandra Santoro, Maurizio Aricò, Daniela Pende, Lorenzo Moretta, Concetta Micalizzi, Patrizia Bertolini, Luigi D. Notarangelo, Carmen De Fusco, Gillian M. Griffiths, Sonia Cannella, Cesare Danesino
Publikováno v:
Blood. 106:2807-2807
Familial hemophagocytic Lymphohistiocytosis (FLH) is a rare disorder characterized by fever, hepatosplenomegaly, cytopenia, hypertriglyceridemia, hypofibrinogenemia and reduced natural killer (NK) cell activity. Several genetic defects have been reco