Search Results - "Roveda, Andrea"

Invasive Pulmonary Aspergillosis in a Sickle Cell Patient Transplant Recipient: A Successful Treatment by Paciaroni, Katia, De Angelis, Gioia, Gallucci, Cristiano, Alfieri, Cecilia, Ribersani, Michela, Roveda, Andrea, Isgrò, Antonella, Marziali, Marco, Aloi, Ivan Pietro, Inserra, Alessandro, Gaziev, Javid, Sodani, Pietro, Lucarelli, Guido

“…Sickle Cell Anaemia (SCA) is the most common inherited blood disorder and is associated with severe morbidity and decreased survival. Allogeneic Haematopoietic…”
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Peripheral red blood cell split chimerism as a consequence of intramedullary selective apoptosis of recipient red blood cells in a case of sickle cell disease by Marziali, Marco, Isgrò, Antonella, Sodani, Pietro, Gaziev, Javid, Fraboni, Daniela, Paciaroni, Katia, Gallucci, Cristiano, Alfieri, Cecilia, Roveda, Andrea, De Angelis, Gioia, Cardarelli, Luisa, Ribersani, Michela, Andreani, Marco, Lucarelli, Guido

“…Allogeneic cellular gene therapy through hematopoietic stem cell transplantation is the only radical cure for congenital hemoglobinopathies like thalassemia…”
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Reduction of intramedullary apoptosis after stem cell transplantation in black african variant of pediatric sickle cell anemia by Isgrò, Antonella, Sodani, Pietro, Marziali, Marco, Gaziev, Javid, Fraboni, Daniela, Paciaroni, Katia, Gallucci, Cristiano, De Angelis, Gioia, Alfieri, Cecilia, Ribersani, Michela, Armiento, Daniele, Roveda, Andrea, Andreani, Marco, Testi, Manuela, Lucarelli, Guido

“…Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment for sickle cell anemia (SCA). We report our experience with…”
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PREVALENCE AND CORRELATES OF ADHERENCE IN CHILDREN AND ADOLESCENTS TREATED WITH GROWTH HORMONE: A MULTICENTER ITALIAN STUDY by Bagnasco, Francesca, Di Iorgi, Natascia, Roveda, Andrea, Gallizia, Annalisa, Haupt, Riccardo, Maghnie, Mohamad

“…To evaluate the self-reported prevalence of poor adherence to recombinant human growth hormone (rhGH) therapy in a large, representative sample of Italian…”
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T cell-depleted hla-haploidentical stem cell transplantation in thalassemia young patients by Sodani, Pietro, Isgrò, Antonella, Gaziev, Javid, Paciaroni, Katia, Marziali, Marco, Simone, Maria Domenica, Roveda, Andrea, De Angelis, Gioa, Gallucci, Cristiano, Torelli, Fabio, Isacchi, Giancarlo, Zinno, Francesco, Landi, Fabiola, Adorno, Gaspare, Lanti, Alessandro, Testi, Manuela, Andreani, Marco, Lucarelli, Guido

“…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…”
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Coagulation parameters and venous thromboembolism in patients with and without COVID-19 admitted to the Emergency Department for acute respiratory insufficiency by Pizzi, Roberto, Gini, Giancarlo, Caiano, Lucia, Castelli, Beniamino, Dotan, Noga, Magni, Federica, Virano, Alexandra, Roveda, Andrea, Bertù, Lorenza, Ageno, Walter

“…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…”
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Purified T-depleted, CD34+ peripheral blood and bone marrow cell transplantation from haploidentical mother to child with thalassemia by Sodani, Pietro, Isgrò, Antonella, Gaziev, Javid, Polchi, Paola, Paciaroni, Katia, Marziali, Marco, Simone, Maria Domenica, Roveda, Andrea, Montuoro, Aldo, Alfieri, Cecilia, De Angelis, Gioia, Gallucci, Cristiano, Erer, Buket, Isacchi, Giancarlo, Zinno, Francesco, Adorno, Gaspare, Lanti, Alessandro, Faulkner, Lawrence, Testi, Manuela, Andreani, Marco, Lucarelli, Guido

“…Fetomaternal microchimerism suggests immunological tolerance between mother and fetus. Thus, we performed primary hematopoietic stem cell transplantation from…”
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Cardiovascular autonomic alterations in hospitalized patients with community-acquired pneumonia by Aliberti, Stefano, Tobaldini, Eleonora, Giuliani, Fabio, Nunziata, Vanessa, Casazza, Giovanni, Suigo, Giulia, D'Adda, Alice, Bonaiti, Giulia, Roveda, Andrea, Queiroz, Andreia, Monzani, Valter, Pesci, Alberto, Blasi, Francesco, Montano, Nicola

“…Alterations of cardiac autonomic control (CAC) are associated with poor outcomes in patients with infectious and non-infectious diseases. No evaluation of CAC…”
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Rapid Increase of CD8+ T Cell Count in Peripheral Blood of Pediatric Patients After HLA-Identical Stem Cell Transplantation for African Sickle Cell Anemia by Isgrò, Antonella, Marziali, Marco, Sodani, Pietro, Gaziev, Javid, Fraboni, Daniela, Paciaroni, Katia, Simone, Maria Domenica, De Angelis, Gioia, Alfieri, Cecilia, Gallucci, Cristiano, Roveda, Andrea, Torelli, Fabio, Cardarelli, Luisa, Ribersani, Michela, Lucarelli, Guido

“…Abstract 4769 Sickle Cell anemia (SCA) remain a disease with high risk of morbidity and early death, especially in African patients. Allogeneic haematopoietic…”
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Decreased Apoptosis in Bone Marrow of Pediatric Patients After HLA-Identical Stem Cell Transplantation for African Sickle Cell Anemia by Isgrò, Antonella, Marziali, Marco, Sodani, Pietro, Gaziev, Javid, Fraboni, Daniela, Paciaroni, Katia, Simone, Maria Domenica, De Angelis, Gioia, Alfieri, Cecilia, Gallucci, Cristiano, Roveda, Andrea, Torelli, Fabio, Cardarelli, Luisa, Ribersani, Michela, Lucarelli, Guido

“…Abstract 4751 In thalassemia patients ineffective erythropoiesis appears to be caused by accelerated apoptosis, in turn caused primarily by deposition of…”
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Sustained and full fetal hemoglobin production after failure of bone marrow transplant in a patient homozygous for beta 0‐thalassemia: A clinical remission despite genetic disease and transplant rejection by Paciaroni, Katia, Gallucci, Cristiano, De Angelis, Gioia, Alfieri, Cecilia, Roveda, Andrea, Lucarelli, Guido

“…An adult patient affected by β0‐thalassemia major underwent allogeneic bone marrow transplant (BMT) from a matched related donor. Forty days after transplant,…”
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A Novel Treatment Protocol Successfully Prevented Graft Rejection and Improved Disease-Free Survival in Class 3 Children with Thalassemia by Gaziev, Javid, Sodani, Pietro, Isgrò, Antonella, Marziali, Marco, Simone, Maria Domenico, Torelli, Fabio, Andreani, Marco, Testi, Manuela, Paciaroni, Katia, Gallucci, Cristiano, Roveda, Andrea, De Angelis, Gioia, Alfieri, Cecilia, Lucarelli, Guido

“…Abstract 150▪▪This icon denotes a clinically relevant abstract Historically, bone marrow transplantation (BMT) in class 3 thalassemia patients has been…”
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T cell-depleted hla-haploidentical stem cell transplantation in thalassemia young patients by Sodani, Pietro, Isgrò, Antonella, Gaziev, Javid, Paciaroni, Katia, Marziali, Marco, Simone, Maria Domenica, Roveda, Andrea, De Angelis, Gioa, Gallucci, Cristiano, Torelli, Fabio, Isacchi, Giancarlo, Zinno, Francesco, Landi, Fabiola, Adorno, Gaspare, Lanti, Alessandro, Testi, Manuela, Andreani, Marco, Lucarelli, Guido

“…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…”
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Sustained and full fetal hemoglobin production after failure of bone marrow transplant in a patient homozygous for beta O-thalassemia: A clinical remission despite genetic disease and transplant rejection by PACIARONI, Katia, GALLUCCI, Cristiano, DE ANGELIS, Gioia, ALFIERI, Cecilia, ROVEDA, Andrea, LUCARELLI, Guido

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Invasive pulmonary aspergillosis in a haematopoietic stem cell transplant recipient with sickle cell disease: a successful treatment by Paciaroni, Katia, De Angelis, Gioia, Gallucci, Cristiano, Alfieri, Cecilia, Ribersani, Michela, Roveda, Andrea, Isgrò, Antonella, Marziali, Marco, Aloi, Ivan Pietro, Inserra, Alessandro, Gaziev, Javid, Sodani, Pietro, Lucarelli, Guido

“…Sickle Cell Anaemia (SCA) is the most common inherited blood disorder and is associated with severe morbidity and decreased survival. Allogeneic Haematopoietic…”
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Late-Onset Hemorrhagic Cystitis in Children After Hematopoietic Stem Cell Transplantation (HSCT) for Thalassemia and Sickle Cell Anemia: A Prospective Evaluation of Polyoma (BK) Virus Infection and Treatment with Cidofovir (CDV) by Gaziev, Javid, Lucarelli, Guido, Germani, Stefano, Paba, Pierpaolo, Perno, Carlo Federico, Miano, Roberto, Bove, Pierluigi, Sodani, Pietro, Isgro, Antonella, Marziali, Marco, Polchi, Paola, Montuoro, Aldo, Paciaroni, Katia, Gallucci, Cristiano, Simone, Maria Domenica, Roveda, Andrea, De Angelis, Gioia, Alfieri, Cecilia

“…Abstract 1133 Poster Board I-155 Hemorrhagic cystitis (HC) is a significant cause of morbidity after allogeneic HSCT. BK virus infection has been associated…”
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Thiotepa in the Conditioning Regimen Decreases Rejection after HLA Identical Allogeneic Marrow Transplantation in Children with Beta Thalassemia Major Aged Less Then 4 Years by Polchi, Paola, Gaziev, Javid, Lucarelli, Guido, Sodani, Pietro, Alfieri, Cecilia, De Angelis, Gioia, Gallucci, Cristiano, Isgro, Antonella, Marziali, Marco, Roveda, Andrea, Paciaroni, Katia

“…BMT in children with beta thalassemia major is the only form of definitive cure with correction of the genetic disease in a relevant proportion of patients,…”
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Bone Marrow Iron Concentration as a Marker of Iron Accumulation and Marrow Expansion in Patients with Beta Thalassemia Major by Polchi, Paola, Palmieri, Rossella, Andreani, Marco, Gaziev, Javid, Alfieri, Cecilia, De Angelis, Gioia, Gallucci, Cristiano, Isgro, Antonella, Marziali, Marco, Paciaroni, Katia, Roveda, Andrea, Sodani, Pietro, Lucarelli, Guido

“…Liver iron concentration (LIC) is a known and accurate marker of iron accumulation and is widely utilized to monitor iron chelation therapy in multiply…”
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High Engraftment Rate after Second Stem Cell Transplantation for Thalassemia: A Prospective Study by Gaziev, Javid, Lucarelli, Guido, Sodani, Pietro, Polchi, Paola, Paciaroni, Katia, Marziali, Marco, Isgro, Antonella, Alfieri, Cecilia, Simone, Maria Domenica, Roveda, Andrea, Montuoro, Aldo, De Angelis, Gioia, Gallucci, Cristiano

“…Unlike hematological malignancies patients with thalassemia have an increased risk of graft failure or rejection occurring in up to 15% of patients after…”
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Haematopoietic stem cell transplantation in Nigerian sickle cell anaemia children patients by Isgrò, Antonella, Paciaroni, Katia, Gaziev, Javid, Sodani, Pietro, Gallucci, Cristiano, Marziali, Marco, Angelis, Gioia De, Alfieri, Cecilia, Ribersani, Michela, Roveda, Andrea, Akinyanju, Olufemi O, Wakama, T Thompson, Olowoselu, Festus Olusola, Adediran, Adewumi, Lucarelli, Guido

“…Sickle cell anaemia (SCA) remains associated with high risks of morbidity and early death. Children with SCA are at high risk for ischaemic stroke and…”
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