Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Marta Claudia Frittoli"'
Autor:
Maria Rosa Lidonnici, Annamaria Aprile, Marta Claudia Frittoli, Giacomo Mandelli, Ylenia Paleari, Antonello Spinelli, Bernhard Gentner, Matilde Zambelli, Cristina Parisi, Laura Bellio, Elena Cassinerio, Laura Zanaboni, Maria Domenica Cappellini, Fabio Ciceri, Sarah Marktel, Giuliana Ferrari
Publikováno v:
Haematologica, Vol 102, Iss 4 (2017)
Externí odkaz:
https://doaj.org/article/1cbe996887dd4a61a85712cff198362b
Autor:
Giulia Tanzi, Ramona Bertoni, Gioachino Caresana, Giuseppina Ferrero, Bruno Drera, Elena Varotti, Marco Ungari, Monica Trombatore, Marino Daniel Gusolfino, Laura Manotti, Marta Claudia Frittoli
Publikováno v:
The American Journal of dermatopathology. 43(3)
Langerhans cell histiocytosis (LCH) is a clonal proliferation of bone-marrow-derived cells, which normally reside as epidermal and mucosal dendritic cells involved in antigen presentation. It is a rare disease more common in children than adults, tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ac395da5038e76f4154598b0af282c
https://pubmed.ncbi.nlm.nih.gov/32769549
https://pubmed.ncbi.nlm.nih.gov/32769549
Autor:
Maddalena Migliavacca, Paola Massariello, Roberto Miniero, Laura Lorioli, Laura Castagnaro, Francesca Tucci, Francesca Fumagalli, Francesco Calzatini, Miriam Casiraghi, Luca Santoleri, Claudia Fossati, Daniele Canarutto, Marcella Facchini, Maria Pia Cicalese, Fabio Ciceri, Alessandra Biffi, Matilde Zambelli, Sarah Marktel, Valeria Calbi, Stefano Zancan, Marta Claudia Frittoli, Paolo Silvani, Gigliola Antonioli, Giulia Consiglieri, Raffaella Milani, Silvia Darin, Francesca Ferrua, Salvatore Recupero, Maria Ester Bernardo, Salvatore Gattillo, Rossana Fiori, Alessandro Aiuti, Federica Barzaghi, Michele Manfredini
Publikováno v:
Bone marrow transplantation
Collection of an adequate amount of autologous haematopoietic stem progenitor cells (HSPC) is required for ex vivo manipulation and successful engraftment for certain inherited disorders. Fifty-seven paediatric patients (age 0.5–11.4 years) underwe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::64af600a2b198d4c7df83ce154616c32
http://www.nature.com/bmt/index.html
http://www.nature.com/bmt/index.html
Autor:
Laura Bellio, Bernhard Gentner, Laura Zanaboni, Matilde Zambelli, Annamaria Aprile, Elena Cassinerio, Sarah Marktel, Ylenia Paleari, Cristina Parisi, Fabio Ciceri, Antonello E. Spinelli, Marta Claudia Frittoli, Maria Domenica Cappellini, Giacomo Mandelli, Giuliana Ferrari, Maria Rosa Lidonnici
For decades, bone marrow (BM) has been the preferred source of hematopoietic stem and progenitor cells (HSPCs) for transplants following myeloablative conditioning. At present, mobilized peripheral blood stem cells are commonly used for transplantati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd84e50a253067a347f8952ea0a4aa1d
Autor:
Maria Rosa, Lidonnici, Annamaria, Aprile, Marta Claudia, Frittoli, Giacomo, Mandelli, Ylenia, Paleari, Antonello, Spinelli, Bernhard, Gentner, Matilde, Zambelli, Cristina, Parisi, Laura, Bellio, Elena, Cassinerio, Laura, Zanaboni, Maria Domenica, Cappellini, Fabio, Ciceri, Sarah, Marktel, Giuliana, Ferrari
Publikováno v:
Haematologica. 102(4)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::88f8f376da110f2be693e5b72c0beff6
https://pubmed.ncbi.nlm.nih.gov/28034992
https://pubmed.ncbi.nlm.nih.gov/28034992
Autor:
Maria Rosa Lidonnici, Marta Claudia Frittoli, Matilde Zambelli, Giuliana Ferrari, Giacomo Mandelli, Annamaria Aprile, Bernhard Gentner, Fabio Ciceri, Maria Domenica Cappellini, Ylenia Paleari, Sarah Marktel, Antonello E. Spinelli, Laura Zanaboni, Elena Cassinerio, Cristina Parisi, Laura Bellio
Publikováno v:
Blood. 128:4709-4709
Over the past decades outcomes of clinical hematopoietic stem cell transplants have established a clear relationship between the sources of hematopoietic stem cells (HSCs) infused and their differential homing and engraftment properties. For a long t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b85be25ecb1a60624ea9cd7399e6ef9a
https://doi.org/10.1182/blood.v128.22.4709.4709
https://doi.org/10.1182/blood.v128.22.4709.4709
Autor:
Marta Claudia Frittoli, Paolo Silvani, Raffaella Milani, Maddalena Migliavacca, Giada Farinelli, Fabio Ciceri, Giovanna Chidini, Anna Camporesi, Roberto Nicoletti, Anna Mandelli, Francesca Ferrua, Edoardo Calderini, Alessandra Biffi, Andrea Assanelli, Alessandro Aiuti, M. P. Cicalese, Maria Ester Bernardo
Publikováno v:
The Journal of Allergy and Clinical Immunology
To the Editor: Chronic granulomatous disease (CGD) is a rare genetic disease caused by defects in genes encoding the subunits of the nicotinamide adenine dinucleotide phosphate oxidase complex.1 Accordingly, patients with CGD are affected by life-thr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5007d867b7d61ecdee2ec9423302409b
https://doi.org/10.1016/j.jaci.2016.01.033
https://doi.org/10.1016/j.jaci.2016.01.033
Autor:
Bernhard Gentner, Annamaria Aprile, Sarah Marktel, Laura Bellio, Ylenia Paleari, Marta Claudia Frittoli, Elena Cassinerio, Fabio Ciceri, Giacomo Mandelli, Laura Zanaboni, Maria Domenica Cappellini, Giuliana Ferrari, Maria Rosa Lidonnici
Publikováno v:
Blood. 126:3069-3069
Over the past decades outcomes of clinical hematopoietic stem cell transplants have established a clear relationship between the sources of hematopoietic stem cells (HSCs) infused and their differential homing and engraftment properties. For a long t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b9b9590a61eb644e42eb69d1e45309db
https://doi.org/10.1182/blood.v126.23.3069.3069
https://doi.org/10.1182/blood.v126.23.3069.3069
Autor:
Marta Claudia Frittoli, Maria Grazia Roncarolo, Erika Biral, Barbara Cappelli, Fabio Ciceri, Giuliana Ferrari, Sarah Marktel, Matilde Zambelli
Publikováno v:
Human gene therapy. 22(4)
beta-Thalassemia is a severe inherited anemia caused by insufficient production of beta-globin chains. Allogeneic hematopoietic stem cell (HSC) transplantation is currently the only cure, and is limited by donor availability and regimen-related toxic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4085a6d42d61b973faf10b3a08b2ed5e
https://pubmed.ncbi.nlm.nih.gov/20979441
https://pubmed.ncbi.nlm.nih.gov/20979441
Autor:
Maria Domenica Cappellini, Erika Biral, Guido Lucarelli, Giovanni Tonon, Giuliana Ferrari, Maria Grazia Roncarolo, Giulietta Maruggi, Riccardo Mezzadra, Marta Claudia Frittoli, Fabrizio Mastropietro, Fulvio Mavilio, Chiara Refaldi, Sarah Marktel, Marco Andreani, Antonio Amato, Emanuela Anna Roselli
beta-Thalassemia is a common monogenic disorder due to mutations in the beta-globin gene and gene therapy, based on autologous transplantation of genetically corrected haematopoietic stem cells (HSCs), holds the promise to treat patients lacking a co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::05fee6e6b9f3692897bc0b1bcaeec8a8