Search Results - "Erer, Buket"

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  1. 1

    Effects of iron overload and hepatitis C virus positivity in determining progression of liver fibrosis in thalassemia following bone marrow transplantation by Angelucci, Emanuele, Muretto, Pietro, Nicolucci, Antonio, Baronciani, Donatella, Erer, Buket, Gaziev, Javid, Ripalti, Marta, Sodani, Pietro, Tomassoni, Silvia, Visani, Giuseppe, Lucarelli, Guido

    Published in Blood (01-07-2002)
    “…To identify the role of iron overload in the natural history of liver fibrosis, we reviewed serial hepatic biopsy specimens taken annually from patients cured…”
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    Journal Article
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    The effects of mesenchymal stem cells on lymphoblastic leukemia cell proliferation by Bozok Cetintas, Vildan, Aktug, Huseyin, Oltulu, Fatih, Keskinoglu, Ahmet, Erer Del Castello, Buket, Taskiran, Dilek

    Published in Journal of B.U. ON. (01-10-2014)
    “…Mesenchymal stem cells (MSCs) represent a new approach to the treatment of several neoplastic or non-neoplastic disorders. Their potential to repair damaged…”
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    Journal Article
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    New approach for bone marrow transplantation in patients with class 3 thalassemia aged younger than 17 years by Sodani, Pietro, Gaziev, David, Polchi, Paola, Erer, Buket, Giardini, Claudio, Angelucci, Emanuele, Baronciani, Donatella, Andreani, Marco, Manna, Marisa, Nesci, Sonia, Lucarelli, Barbarella, Clift, Reginald A., Lucarelli, Guido

    Published in Blood (15-08-2004)
    “…When prepared for transplantation with busulfan (BU) 14 mg/kg and cyclophosphamide (CY) 120 to 160 mg/kg, patients with thalassemia in risk class 3, aged…”
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    Journal Article
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    Phlebotomy to reduce iron overload in patients cured of thalassemia by bone marrow transplantation by ANGELUCCI, E, MURETTO, P, LUCARELLI, G, RIPALTI, M, BARONCIANI, D, ERER, B, GALIMBERTI, M, GIARDINI, C, GAZIEV, D, POLCHI, P

    Published in Blood (01-08-1997)
    “…Abstract In thalassemia after successful bone marrow transplantation (BMT), iron overload remains an important cause of morbidity. After BMT, patients have…”
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    Journal Article
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    Preliminary Experience of the Pakistani Network for the Cure and Prevention of Thalassaemia Supported by the Cure2Children Foundation by Faulkner, Lawrence B., Shamsi, Tahir, Ansari, Saqib, Farzana, Tasneem, Khalid, Sadaf, Clemente, Luigi, Yaqub, Naila, Zafar, Tahira, Kamran, Rashid, Iqbal, Yasir, Sodani, Pietro, Gallucci, Cristiano, Erer, Buket, Lucarelli, Guido

    Published in Blood (20-11-2009)
    “…Abstract 4331 Since May 2008, the Cure2Children Foundation has supported both financially and professionally a network of centers in Pakistan for stem cell…”
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    Journal Article
  8. 8

    Bone Marrow Transplantation in Thalassemia: The Experience of Pesaro by LUCARELLI, GUIDO, GALIMBERTI, MARIA, GIARDINI, CLAUDIO, POLCHI, PAOLA, ANGELUCCI, EMANUELE, BARONCIANI, DONATELLA, ERER, BUKET, GAZIEV, DJAVID

    Published in Annals of the New York Academy of Sciences (01-06-1998)
    “…: Early trials of allogenic bone marrow transplantation (BMT) for homozygous β thalassemia and the analyses of results of transplantation in patients under 17…”
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    Journal Article
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    Purified T Depleted Peripheral Blood and Bone Marrow Cd34 Transplantation from Haploidentical Mother to Child with Thalassemia by Sodani, Pietro, Erer, Buket, Gaziev, Javid, Polchi, Paola, Roveda, Andrea, Spitaleri, Luca, Pagliai, Francesca, Paciaroni, Katia, Adorno, Gaspare, Lanti, Alessandro, Isacchi, Giancarlo, Zinno, Francesco, Lucarelli, Guido

    Published in Blood (16-11-2006)
    “…Approximately 60% of thalassemic patients can not apply to “gene therapy today” which the insertion of one allogenic HLA identical stem cell into the empty…”
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    Journal Article
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    Long-Term Outcome after Bone Marrow Transplantation for Adult Thalassemia by Gaziev, Javid, Sodani, Pietro, Roveda, Andrea, Spitaleri, Luca, Montuoro, Aldo, Simone, Maria Domenica, Erer, Buket, Polchi, Paola, Lucarelli, Guido

    Published in Blood (16-11-2005)
    “…Advances in management of thalassemia have increased the proportion of patients living into adulthood. However, disease and treatment related complications in…”
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    Journal Article
  12. 12

    Immuno Haematological Reconstitution after T-Cell-Depleted HLA-Haploidentical Stem Cell Transplantation for Thalassemia by Isgrò, Antonella, Erer, Buket, Sodani, Pietro, Polchi, Paola, Marziali, Marco, Leti, Wilma, Gramiccioni, Claudia, De Santis, Wladimiro, Campagna, Massimo, Del Giudice, Giorgia, Caterina Sirianni, Maria, Aiuti, Fernando, Lucarelli, Guido

    Published in Blood (16-11-2006)
    “…Background. We evaluated haematological and immunological characteristics of four thalassemia patients after T-cell-depleted HLA-haploidentical stem cell…”
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    Journal Article
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    Phlebotomy to Reduce Iron Overload in Patients Cured of Thalassemia by Bone Marrow Transplantation by Angelucci, Emanuele, Muretto, Pietro, Lucarelli, Guido, Ripalti, Marta, Baronciani, Donatella, Erer, Buket, Galimberti, Maria, Giardini, Claudio, Gaziev, Djavid, Polchi, Paola

    Published in Blood (01-08-1997)
    “…In thalassemia after successful bone marrow transplantation (BMT), iron overload remains an important cause of morbidity. After BMT, patients have normal…”
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    Journal Article
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    Graft-versus-host disease after bone marrow transplantation for thalassemia : An analysis of incidence and risk factors by GAZIEV, D, POLCHI, P, GALIMBERTI, M, ANGELUCCI, E, GIARDINI, C, BARONCIANI, D, ERER, B, LUCARELLI, G

    Published in Transplantation (27-03-1997)
    “…We analyzed risk factors in 724 patients evaluable for acute graft-versus-host disease (GVHD) and in 614 patients evaluable for chronic GVHD who had received…”
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    Journal Article
  16. 16

    Treatment of Iron Overload in the "Ex-Thalassemic": Report from the Phlebotomy Program by ANGELUCCI, EMANUELE, MURETTO, PIETRO, LUCARELLI, GUIDO, RIPALTI, MARTA, BARONCIANI, DONATELLA, ERER, BUKET, GALIMBERTI, MARIA, ANNIBALI, MAURO, GIARDINI, CLAUDIO, GAZIEV, DJAVID, RAPA, SIMONA, POLCHI, PAOLA

    Published in Annals of the New York Academy of Sciences (30-06-1998)
    “…After successful marrow transplantation (BMT) iron overload remains an important cause of morbidity in Thalassemia. After BMT, patients have normal…”
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    Journal Article
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    Treatment of Iron Overload in the “Ex‐Thalassemic”: Report from the Phlebotomy Programa by ANGELUCCI, EMANUELE, MURETTO, PIETRO, LUCARELLI, GUIDO, RIPALTI, MARTA, BARONCIANI, DONATELLA, ERER, BUKET, GALIMBERTI, MARIA, ANNIBALI, MAURO, GIARDINI, CLAUDIO, GAZIEV, DJAVID, RAPA, SIMONA, POLCHI, PAOLA

    Published in Annals of the New York Academy of Sciences (01-06-1998)
    “…: After successful marrow transplantation (BMT) iron overload remains an important cause of morbidity in Thalassemia. After BMT, patients have normal…”
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    Journal Article
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