Zobrazeno 1 - 10
of 43
pro vyhledávání: '"Gioia De Angelis"'
Autor:
Javid Gaziev, Antonella Isgrò, Pietro Sodani, Katia Paciaroni, Gioia De Angelis, Marco Marziali, Michela Ribersani, Cecilia Alfieri, Alessandro Lanti, Tiziana Galluccio, Gaspare Adorno, Marco Andreani
Publikováno v:
Blood Advances, Vol 2, Iss 3, Pp 263-270 (2018)
Abstract: We examined outcomes of haploidentical hematopoietic cell transplantation (haplo-HCT) using T-cell receptor αβ+ (TCRαβ+)/CD19+-depleted grafts (TCR group, 14 patients) in children with hemoglobinopathies. Patients received a preparative
Externí odkaz:
https://doaj.org/article/723cc819f11041e897379fe1fb554f1d
Autor:
Antonella Isgrò, Javid Gaziev, Marco Marziali, Katia Paciaroni, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Festus Olusola Olowoselu, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 9, Iss 1, Pp e2017030-e2017030 (2017)
Children with sickle cell anemia (SCA) are prone to invasive infections caused by S. pneumonia, H. influenzae, and Plasmodium falciparum. The presence of asthma increases the risk of mortality, and it has been shown an association between the presenc
Externí odkaz:
https://doaj.org/article/eece0808eaad4e048ff5c25e18f9fe0e
Autor:
Katia Paciaroni, Gioia De Angelis, Cristiano Gallucci, Cecilia Alfieri, Michela Ribersani, Andrea Roveda, Antonella Isgrò, Marco Marziali, Ivan Pietro Aloi, Alessandro Inserra, Javid Gaziev, Pietro Sodani, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 7, Iss 1, Pp e2015006-e2015006 (2015)
Sickle Cell Anaemia (SCA) is the most common inherited blood disorder and is associated with severe morbidity and decreased survival. Allogeneic Haematopoietic Stem Cell Transplantation (HSCT) is the only curative approach. Nevertheless the decision
Externí odkaz:
https://doaj.org/article/0a726cdebb4d4721b7ae2ce4b32b0f63
Autor:
Marco Marziali, Antonella Isgrò, Pietro Sodani, Javid Gaziev, Daniela Fraboni, Katia Paciaroni, Cristiano Gallucci, Cecilia Alfieri, Andrea Roveda, Gioia De Angelis, Luisa Cardarelli, Michela Ribersani, Marco Andreani, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 6, Iss 1, Pp e2014066-e2014066 (2014)
Allogeneic cellular gene therapy through hematopoietic stem cell transplantation is the only radical cure for congenital hemoglobinopathies like thalassemia and sickle cell anemia. Persistent mixed hematopoietic chimerism (PMC) has been described in
Externí odkaz:
https://doaj.org/article/e65dccd780f84903ad8c4c54612fc422
Autor:
Antonella Isgrò, Pietro Sodani, Marco Marziali, Javid Gaziev, Daniela Fraboni, Katia Paciaroni, Cristiano Gallucci, Gioia De Angelis, Cecilia Alfieri, Michela Ribersani, Daniele Armiento, Andrea Roveda, Marco Andreani, Manuela Testi, Guido Lucarelli
Publikováno v:
Mediterranean Journal of Hematology and Infectious Diseases, Vol 6, Iss 1, Pp e2014054-e2014054 (2014)
Background and Purpose: Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment for sickle cell anemia (SCA). We report our experience with transplantation in children with the Black African variant of SCA and the eff
Externí odkaz:
https://doaj.org/article/d2c4a673834a4ad6935e7ce29c3b2f5a
Autor:
Giulio Trapè, Gioia De Angelis, Marco Morucci, Michela Tarnani, Cinzia De Gregoris, Ambra Di Veroli, Valentina Panichi, Giuseppe Topini, Loredana Bassi, Raffaella Isidori, Monica Poscente, Vincenza Innocenti, Elisa Emanueli Cippitelli, Roberta Talucci, Silvia Bertelli, Alessandra Crocicchia, Annalisa Lippi, Giulia Pezzuti, Michela Fuschino, Raffaella Randi, Cristina Mastini, Silvia Ciambella, Gloria Pessina, Marco Montanaro, Roberto Latagliata
Publikováno v:
European Journal of Haematology.
Autor:
Elisa Emanueli Cippitelli, Vincenza Innocenti, Gioia De Angelis, Silvia Bertelli, Roberta Talucci, Roberta Perazzini, Roberta Burla, Valentina Panichi, Giuseppe Topini, Ambra Di Veroli, Alessia Fiorini, Caterina Mercanti, Fiammetta Natalino, Caterina Stefanizzi, Cinzia De Gregoris, Michela Tarnani, Marco Morucci, Cristina Mastino, Giulio Trapè, Marco Montanaro, Roberto Latagliata, Silvia Ciambella
Publikováno v:
Blood. 140:2404-2405
Autor:
Sara Moccia, Gioia De Angelis, Marcello Naldini, Emanuele Frontoni, Daniele Berardini, Lucia Migliorelli
Publikováno v:
ISCC
Monitoring children with Autism Spectrum Dis-order (ASD) during the execution of the Applied Behaviour Analysis (ABA) program is crucial to assess the progresses while performing actions. Despite its importance, this monitoring procedure still relies
Autor:
Roberto Latagliata, Loredana Bassi, Monica Poscente, Silvia Ciambella, Giulio Trapè, Michela Tarnani, Michela Fuschino, Raffaella Isidori, Silvia Bertelli, Cristina Mastino, Giuseppe Topini, Valentina Panichi, Roberta Talucci, Cinzia De Gregoris, Alessandra Crocicchia, Gloria Pessina, Vincenza Innocenti, Gioia De Angelis, Elisa Emanueli Cippitelli, Ambra Di Veroli, Marco Montanaro, Marco Morucci, Raffaella Randi, Giulia Pezzuti, Annalisa Lippi
Publikováno v:
Blood. 138:4042-4042
Introduction Treatment with Hypometilating Agents (HMA) of unfit patients (pts) with Acute Myelogenous Leukemia (AML) and High-Risk Myelodysplastic Syndromes (HR-MDS) is often difficult in the standard Day-Hospital (DH) setting, due to the number of
Autor:
Alessia Fiorini, Michela Tarnani, Silvia Bertelli, Vincenza Innocenti, Valentina Panichi, Giulio Trapè, Roberta Talucci, Assunta Silvestri, Cristina Mastino, Roberto Latagliata, Gioia De Angelis, Fiammetta Natalino, Silvia Ciambella, Caterina Mercanti, Elisa Emanueli Cippitelli, Marco Morucci, Giuseppe Topini, Fabio Stagno, Marco Montanaro, Ambra Di Veroli
Publikováno v:
Blood
Introduction In the Viterbo province (3612 Km 2 divided into 60 municipalities) is operative a Domiciliary Hematologic Care Unit (DHCU) for clinical assistance to frail patients (pts) with hemopathies: DHCU nursing activity is done by 4 units who wer