Zobrazeno 1 - 10
of 47
pro vyhledávání: '"Am Risitano"'
Autor:
AR Fonseca, CC Justino, VC Molla, PE Yamakawa, IB Rabelo, A Hill, L Arnold, R Kelly, M Griffin, T Munir, E Velloso, T Dalessandro, AM Risitano, P Scheinberg, A Kulasekararaj, C Arrais-Rodrigues
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss , Pp S17- (2023)
This multicenter international retrospective analysis aimed to evaluate the efficacy and safety of subcutaneous alemtuzumab (ALZ) as an alternative immunosuppressive therapy for aplastic anemia (AA). The study included 57 with AA patients who receive
Externí odkaz:
https://doaj.org/article/9019b3e2c3ce41f898c65193ae4a950e
Autor:
Maddalena Raia, D Schiavone, F. Rubba, Scamardo, Gaetano Buonocore, Davide Castrianni, L Del Vecchio, G D'Onofrio, Am Risitano, Maria Triassi
Publikováno v:
European Journal of Public Health. 27
Fanconi anemia (FA) is the most frequent inherited cause of bone marrow failure. Most FA patients experience hematopoietic stem cell attrition and cytopenia during childhood. Allogeneic hematopoietic stem cell transplantation (HSCT) remains the only
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::22b54d247ca884284ecb078a64119b0a
https://doi.org/10.1016/b978-0-12-804152-9.00016-6
https://doi.org/10.1016/b978-0-12-804152-9.00016-6
Autor:
Am Risitano, C. De Caprio, Franco Contaldo, S. Marotta, L. Marano, A. De Rosa, Fabrizio Pasanisi
Publikováno v:
Nutrition. 65:6
Assessment of the need of parenteral nutrition (PN) for patients undergoing allogeneic Haematopoietic Stem Cell Transplantation (HSCT) and effectiveness of nutritional support. 41 consecutive patients (20 females, 21 males) undergoing allogenic HSCT
Autor:
Patrizia Ricci, Am Risitano, G. De Rosa, L Del Vecchio, Bruno Rotoli, Jp Maciejewski, Carmine Selleri, Anna Maria Raiola, G Varriale, P Della Cioppa, Marco Picardi, Luigiana Luciano, L Pezzullo
Publikováno v:
Scopus-Elsevier
We investigated bone marrow (BM) and circulating (PB) hematopoietic progenitor cells in 37 normal donors and in 25 patients 1 to 8 years after successful allogeneic bone marrow transplant. At the time of testing, transplanted patients had normal bloo
Autor:
Hubert Schrezenmeier, Am Risitano
Publikováno v:
Bone marrow transplantation. 48(2)
Antithymocyte globulin (ATG)-based immunosuppression remains the standard immunosuppressive therapy (IST) for aplastic anemia (AA) patients lacking a sibling donor; however, treatment failures are relatively frequent, including about one-quarter to o
Acquired bone marrow failure syndromes (BMFS) are a heterogeneous group of hematological disorders characterized by impaired bone marrow function and subsequent cytopenia of one or more blood cell lineages [1,2]. The well-accepted pathogenic mechanis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2d27c764825cc1d7c8b89a2db979da6
http://hdl.handle.net/11588/569386
http://hdl.handle.net/11588/569386
Publikováno v:
Mini reviews in medicinal chemistry. 11(6)
Paroxysmal nocturnal hemoglobinuria (PNH) is a hematological disorder characterized by complementmediated hemolytic anemia, thrombophilia and bone marrow failure. The clinical hallmark of PNH is evident chronic hemolysis due to the absence of the com
Autor:
Bakhtiari, Tahereh1 (AUTHOR), Ahmadvand, Mohammad2 (AUTHOR) mahmadvand@sina.tums.ac.ir, Yaghmaie, Marjan3 (AUTHOR), Sadeghi, Alireza4 (AUTHOR), Mousavi, Seied Asadollah2 (AUTHOR), Rostami, Tahereh5 (AUTHOR) Trostami@sina.tums.ac.ir, Ganjalikhani-Hakemi, Mazdak1,6 (AUTHOR) mghakemi@med.mui.ac.ir
Publikováno v:
BMC Immunology. 6/20/2023, Vol. 24 Issue 1, p1-13. 13p.
Autor:
Grubic, Zorana1 zgrubic@kbc-zagreb.hr, Burek Kamenaric, Marija1, Maskalan, Marija1, Durakovic, Nadira2, Vrhovac, Radovan2, Stingl Jankovic, Katarina1, Serventi Seiwerth, Ranka2, Zunec, Renata1
Publikováno v:
International Journal of Laboratory Hematology. Jun2022, Vol. 44 Issue 3, p547-557. 11p.