Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Andrea Roveda"'
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:
Pietro Sodani, Antonella Isgrò, Javid Gaziev, Katia Paciaroni, Marco Marziali, Maria Domenica Simone, Andrea Roveda, Gioa De Angelis, Cristiano Gallucci, Fabio Torelli, Giancarlo Isacchi, Francesco Zinno, Fabiola Landi, Gaspare Adorno, Alessandro Lanti, Manuela Testi, Marco Andreani, Guido Lucarelli
Publikováno v:
Pediatric Reports, Pp e12-e12 (2011)
The cure for thalassemia involves correcting the genetic defect in a hematopoietic stem cell that results in reduced or absent β-globin synthesis and an excess of α-globin dimers. Intracellular precipitation and accumulation of α- dimers results i
Externí odkaz:
https://doaj.org/article/77e06a9cabcb4035aa45d7d6454466be
Autor:
Lorenza Bertù, Lucia Caiano, Alexandra Virano, Beniamino Castelli, Giancarlo Gini, Andrea Roveda, Roberto Pizzi, Noga Dotan, Federica Magni, Walter Ageno
Publikováno v:
Thrombosis Research
Background In the recent outbreak of COVID-19 pandemic, increased D-dimer levels and high rates of venous thromboembolic events were reported. We aimed to compare coagulation parameters on admission between COVID-19 patients and non-COVID-19 patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ce081de0f3599b75f195064221b5117
http://europepmc.org/articles/PMC7468277
http://europepmc.org/articles/PMC7468277
Autor:
Cecilia Alfieri, Wilma Leti, Gaspare Adorno, Daniela Fraboni, Marco Andreani, Alessandro Lanti, Giancarlo Isacchi, Buket Erer, Fernando Aiuti, Guido Lucarelli, Javid Gaziev, Francesco Zinno, Marco Marziali, Katia Paciaroni, Antonella Isgrò, Pietro Sodani, Andrea Roveda, Maria Domenica Simone, Cristiano Gallucci, Paola Polchi, Gioia De Angelis
Publikováno v:
Biology of Blood and Marrow Transplantation. 16(11):1557-1566
To analyze immunohematologic reconstitution, particularly of natural killer (NK) cells, we evaluated 13 β-thalassemia patients after 20 and 60 days and 1 year posttransplantation with T cell-depleted HLA-haploidentical stem cells. We assessed lympho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a3a7b657b54aae39f8f90571ad185ec
Autor:
Marco Andreani, Pietro Sodani, Maria Domenica Simone, Javid Gaziev, Andrea Roveda, Katia Paciaroni, Cristiano Gallucci, F Saltarelli, Guido Lucarelli, Marco Marziali, Antonella Isgrò, C Alfieri, G De Angelis, F Torelli
Publikováno v:
Bone marrow transplantation. 47(2)
Many patients with thalassemia have been cured with BMT since the first successful transplant in 1981. Allogeneic stem cell gene therapy is the only treatment option for patients with sickle cell anemia (SCA). A total of 11 patients with a median age
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8d1496be18deef044c47d2b65313f009
https://pubmed.ncbi.nlm.nih.gov/21499319
https://pubmed.ncbi.nlm.nih.gov/21499319
Autor:
Nicola Daniele, Pietro Sodani, Marco Andreani, Marco Marziali, Andrea Roveda, Katia Paciaroni, Manuela Testi, Javid Gaziev, Antonella Isgrò, Alessandro Lanti, C Alfieri, G Del Proposto, Gaspare Adorno, Maria Domenica Simone, Guido Lucarelli, Cristiano Gallucci, F Saltarelli, G De Angelis
Publikováno v:
Bone marrow transplantation. 47(1)
We evaluated the incidence of GVHD, risk factors and the impact of graft composition on acute GVHD (aGVHD) in 92 children who underwent BMT for thalassemia following busulfan/cyclophosphamide (BUCY)-based conditioning regimens and GVHD prophylaxis wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3687218f26fbcb326b86fc81767e6e3d
https://pubmed.ncbi.nlm.nih.gov/21317935
https://pubmed.ncbi.nlm.nih.gov/21317935
Autor:
Carlo Federico Perno, Pierluigi Bove, Roberto Miano, Guido Lucarelli, Antonella Isgrò, Cecilia Alfieri, Katia Paciaroni, Javid Gaziev, P Paba, Marco Marziali, Andrea Roveda, Stefano Germani, Pietro Sodani, Cristiano Gallucci, Maria Domenica Simone, Gioia De Angelis
Little is known about late-onset hemorrhagic cystitis (HC) in children, its relationship to BK virus, and treatment with cidofovir (CDV) following hematopoietic stem cell transplantation (HSCT). We prospectively investigated BK virus reactivation in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7cc6d4486ca26b85dd2bc375ef1dda4
http://hdl.handle.net/2108/41408
http://hdl.handle.net/2108/41408
Autor:
Gioia De Angelis, Alessandro Lanti, Gaspare Adorno, Cecilia Alfieri, Manuela Testi, Javid Gaziev, Lawrence Faulkner, Andrea Roveda, Buket Erer, Giancarlo Isacchi, Cristiano Gallucci, Marco Marziali, Aldo Montuoro, Katia Paciaroni, Guido Lucarelli, Antonella Isgrò, Francesco Zinno, Paola Polchi, Maria Domenica Simone, Marco Andreani, Pietro Sodani
Fetomaternal microchimerism suggests immunological tolerance between mother and fetus. Thus, we performed primary hematopoietic stem cell transplantation from a mismatched mother to thalassemic patient without an human leukocyte antigen–identical d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9288451a8f207c7f02691f89778cc64
http://hdl.handle.net/2108/56220
http://hdl.handle.net/2108/56220