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Journal Articles

Efficacy of Thalidomide in the Treatment of Severe Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT): Preliminary Results of an Ongoing Study

Carlo L Balduini, Francesca Bellistri, Fabio Pagella, Francesco Chu, Elina Matti, Giuseppe Spinozzi, Federica Ornati, Cecilia Canzonieri, Carla Olivieri, Cesare Danesino, Marco Benazzo, Rosangela Invernizzi

Blood (2012) 120 (21): 629.

https://doi.org/10.1182/blood.V120.21.629.629

Published: 2012

Journal Articles

MUNC13–4 Mutations in Patients with Hemophagocytic Lymphohistiocytosis Are Scattered over the Functional Domains of the Protein.

Alessandra Santoro, Sonia Cannella, Giovanna Bossi, Federico Gallo, Antonino Trizzino, Daniela Pende, Francesco Dieli, Giuseppa Bruno, Jane C. Stinchcombe, Caterina Putti, Carmela De Fusco, Cesare Danesino, Lorenzo Moretta, Luigi D. Notarangelo, Gillian Griffiths, Maurizio Aricò

Blood (2006) 108 (11): 1249.

https://doi.org/10.1182/blood.V108.11.1249.1249

Published: 2006

Journal Articles

Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function

Rita Clementi, Annalisa Chiocchetti, Giuseppe Cappellano, Elisa Cerutti, Massimo Ferretti, Elisabetta Orilieri, Irma Dianzani, Marina Ferrarini, Marco Bregni, Cesare Danesino, Valeria Bozzi, Maria Caterina Putti, Franco Cerutti, Angela Cometa, Franco Locatelli, Rita Maccario, Ugo Ramenghi, Umberto Dianzani

Blood (2006) 108 (9): 3079–3084.

https://doi.org/10.1182/blood-2006-02-001412

Published: 2006

Journal Articles

Novel Munc13-4 Mutations in Patients with Hemophagocytic Lymphohistiocytosis.

Alessandra Santoro, Sonia Cannella, Antonino Trizzino, Cesare Danesino, Daniela Pende, Carmen De Fusco, Concetta Micalizzi, Patrizia Bertolini, Lorenzo Moretta, Luigi D. Notarangelo, Gillian M. Griffiths, Maurizio Aricò

Blood (2005) 106 (11): 2807.

https://doi.org/10.1182/blood.V106.11.2807.2807

Published: 2005

Journal Articles

A proportion of patients with lymphoma may harbor mutations of the perforin gene

Rita Clementi, Franco Locatelli, Loïc Dupré, Alberto Garaventa, Lorenzo Emmi, Marco Bregni, Graziella Cefalo, Antonia Moretta, Cesare Danesino, Margherita Comis, Andrea Pession, Ugo Ramenghi, Rita Maccario, Maurizio Aricò, Maria Grazia Roncarolo

Blood (2005) 105 (11): 4424–4428.

https://doi.org/10.1182/blood-2004-04-1477

Published: 2005

Journal Articles

TNF-α-238GA, IL-1α-889CC and IL-10–819CC Polymorphisms Confere an Increased Risk to Develop Multisystem Langerhans Cell Histiocytosis.

Paola De Filippi, Cesare Danesino, Diego Ferrarese, Annalisa De Silvestri, Carla Badulli, Antonino Trizzino, Paola Fidani, Alberto Garaventa, Alessandra Lombardi, Mariaclara Cuccia, Miryam Martinetti, Maurizio Aricò

Blood (2004) 104 (11): 1331.

https://doi.org/10.1182/blood.V104.11.1331.1331

Published: 2004

Journal Articles

Inherited Perforin and Fas Mutations in a Patient with Autoimmune Lymphoproliferative Syndrome and Lymphoma.

Rita Clementi, Lorenzo Dagna, Umberto Dianzani, Loic Dupre, Irma Dianzani, Fabio Ciceri, Rita Maccario, Franco Locatelli, Cesare Danesino, Marina Ferrarini, Marco Bregni

Blood (2004) 104 (11): 1379.

https://doi.org/10.1182/blood.V104.11.1379.1379

Published: 2004

Journal Articles

Patients with Lymphoma May Harbor Mutations of the Perforin Gene.

Rita Clementi, M.D., Franco Locatelli, M.D., Loic Dupre, PhD, Alberto Garaventa, M.D., Lorenzo Emmi, M.D., Marco Bregni, M.D., Graziella Cefalo, M.D., Antonia Moretta, PhD, Cesare Danesino, M.D., Margherita Comis, M.D., Andrea Pession, M.D., Ugo Ramenghi, M.D., Rita Maccario, PhD, Maurizio Arico’, M.D., Maria Grazia Roncarolo, M.D.

Blood (2004) 104 (11): 1358.

https://doi.org/10.1182/blood.V104.11.1358.1358

Published: 2004

Journal Articles

Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations

Rita Clementi, Lorenzo Emmi, Rita Maccario, Francesco Liotta, Lorenzo Moretta, Cesare Danesino, Maurizio Aricò

Blood (2002) 100 (6): 2266.

https://doi.org/10.1182/blood-2002-04-1030

Published: 2002

Journal Articles

Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene

Maurizio Arico, Shinsaku Imashuku, Rita Clementi, Shigeyoshi Hibi, Tomoko Teramura, Cesare Danesino, Daniel A. Haber, Kim E. Nichols

Blood (2001) 97 (4): 1131–1133.

https://doi.org/10.1182/blood.V97.4.1131

Published: 2001

NARROW

Efficacy of Thalidomide in the Treatment of Severe Recurrent Epistaxis in Hereditary Hemorrhagic Telangiectasia (HHT): Preliminary Results of an Ongoing Study

MUNC13–4 Mutations in Patients with Hemophagocytic Lymphohistiocytosis Are Scattered over the Functional Domains of the Protein.

Variations of the perforin gene in patients with autoimmunity/lymphoproliferation and defective Fas function

Novel Munc13-4 Mutations in Patients with Hemophagocytic Lymphohistiocytosis.

A proportion of patients with lymphoma may harbor mutations of the perforin gene

TNF-α-238GA, IL-1α-889CC and IL-10–819CC Polymorphisms Confere an Increased Risk to Develop Multisystem Langerhans Cell Histiocytosis.

Inherited Perforin and Fas Mutations in a Patient with Autoimmune Lymphoproliferative Syndrome and Lymphoma.

Patients with Lymphoma May Harbor Mutations of the Perforin Gene.

Adult onset and atypical presentation of hemophagocytic lymphohistiocytosis in siblings carrying PRF1 mutations

Hemophagocytic lymphohistiocytosis due to germline mutations in SH2D1A, the X-linked lymphoproliferative disease gene

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American Society of Hematology

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ASH Publications

American Society of Hematology

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