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pro vyhledávání: '"G, Schilirò"'
Akademický článek
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Akademický článek
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Publikováno v:
Blood. 90:1226-1232
The aims of this study were twofold: (1) to assess the marrow of patients with T-lineage acute lymphoblastic leukemia (T-ALL) for the presence of molecular residual disease (MRD) at different times after diagnosis and determine its value as a prognos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cda881a0ef2dba982972c60487ccdc07
https://doi.org/10.1182/blood.v90.3.1226.1226_1226_1232
https://doi.org/10.1182/blood.v90.3.1226.1226_1226_1232
Autor:
R. Testa, Andreas Foudoulakis, Shoji Kume, Hiroshi Fukushima, Akira Andoh, Masumi Yoda-Endo, Gyu Bog Choi, Fotini Markidou, Motohiko Okano, Massimo Brisigotti, Kohzoh Imai, Yutaka Yatomi, Claus Lindbjerg Andersen, Helen A. Papadaki, Attilio Rovelli, Norihiko Amemiya, Cesare Romano, Yoshihide Fujiyama, Siu-huie Lin, Jin-hwang Liu, Amnon Cohen, Jin-Hyuk Choi, I-ting Yu, Asako Mizoe, Tadao Bamba, Jørn Koch, Woon Sup Han, Po-min Chen, Bent Pedersen, G. Corneo, Serafettin Kirazli, Z. Jakovlevska, Fumiyasu Nakamura, Yoshiro Matsumoto, O.I. Özcebe, Ruey-kuen Hsieh, Koharik Minas Bajakian, Masayuki Yamamoto, Tsutomu Yuminamochi, Maria Rita Castellani, F. Rossini, George D. Eliopoulos, T.H.J. Huisman, Sheng Fan, Cornelio Uderzo, Tohru Takahashi, I. Casaroli, Masaaki Adachi, Hitoshi Minamiguchi, G. Schilirò, Despina Kyriakou, Johnny Hindkjær, G.D. Efremov, Jack R. Davis, Ki Nam Shim, N.S. Smetanina, Michael G. Alexandrakis, Geoffrey M. Thiele, Kasim Omar Ardati, Paolo Dodero, Tzeon-jye Chiou, Knud Bendix Hansen, Seung Yon Baek, Yuji Hinoda, A. Di Cataldo, Keiko Hodohara, P. Maffè, Sun Hee Sung, Takeshi Endo, E.M. Pogliani, Semra Dündar, L.-H. Gu, Yasushi Adachi, Yukio Ozaki, Khaled S. Tabbara, Ibrahim C. Haznedaroglu
Publikováno v:
Acta Haematologica. 97:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50ad219034cb7d148e4adfea664c632a
https://doi.org/10.1159/000203681
https://doi.org/10.1159/000203681
Publikováno v:
American Journal of Hematology. 33:81-85
The clinical and hematological features of 202 Sicilian subjects with sickle cell disease are reported, 41 being homozygous for beta s (beta s beta s), 64 with beta zero thal beta s (beta zero beta s), and 97 beta+ thal beta s (beta+ beta s). Analysi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2735be7eb5a7ac08b3dcb3b49a14ab45
https://doi.org/10.1002/ajh.2830330202
https://doi.org/10.1002/ajh.2830330202
Autor:
Hans Bäck, Kaoru Nagata, J. Grozdea, Maurizio Zampetti, Sultan T. Al-Sedairy, M. Lakomek, Stefano Sacchi, M. Mancuso, G. Schilirò, J.D. Norton, Stefano Calvieri, Toshiya Suzuki, Stig Rödjer, R. Bierme, P.J. Browett, A. Brisson-Lougarre, Mohammed A. Hannan, P. Samperi, Giuliana De Sanctis, J. Martin, Giovanni Emilia, Donovan P. Gibson, Maged H. Amer, Pasquale Tripputi, Yasufumi Imai, René van de Griend, J.G. Seidman, Randall F. Holcombe, Yoko Yamashita, B.A. Neubauer, A Vecchi, Rosina Longo, Jan Westin, Ragnar Lindblad, S. Alie-Daram, Patrizia Zucchini, Sandra Morselli, Shuji Tohda, Reinder.L.H. Bolhuis, S.W. Eber, Giuseppe Torelli, D. Colomer, H.E. Heslop, W. Schröter, Andrea Fattorossi, M. Gahr, M.A. Pujades, Licia Selleri, J.Ll. Vives-Corrons, Gianmarco Corneo, R. Testa, A.B. Mehta, Siew-Lan Ang, Paola Temperani, Umberto Torelli, Thomas J. McGarry, H. Vergnes, Nobuo Nara
Publikováno v:
Acta Haematologica. 83:I-IV
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ee5e70bcf3c60fc58df1af30da76f3b
https://doi.org/10.1159/000205199
https://doi.org/10.1159/000205199
Autor:
P, Samperi, G, Schilirò
Publikováno v:
Minerva pediatrica. 54(6)
Sickle cell disease adds relevant problems to the physical, emotional and social changes that normally occur during adolescence. Specific physical characteristics and complications of the disease can hinder the social and emotional adjustment of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0ef2ab248d132832f3001f9d4d02538d
https://pubmed.ncbi.nlm.nih.gov/12388939
https://pubmed.ncbi.nlm.nih.gov/12388939
Publikováno v:
Haematologica. 86(12)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::8bfeef1e4a3d20a46c8c1932d026f228
https://pubmed.ncbi.nlm.nih.gov/11726326
https://pubmed.ncbi.nlm.nih.gov/11726326
Autor:
C L, Harteveld, J, Traeger-Synodinos, A, Ragusa, M, Fichera, E, Kanavakis, C, Kattamis, P, Giordano, G, Schilirò, L F, Bernini
Publikováno v:
Haematologica. 86(1)
The occurrence of Hb CS is usually limited to the geographic area which includes Southern China and South East Asia. In 1968 Hb CS was also found to occur in the Mediterranean area where it was originally described as Hb Athens. We investigated the i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::547746f1021caa77ae4cf2b394c56f2e
https://pubmed.ncbi.nlm.nih.gov/11146568
https://pubmed.ncbi.nlm.nih.gov/11146568
Children with leukemia undergo painful procedures such as lumbar puncture and bone marrow aspiration. To overcome pain, certain units offer total anesthesia; others offer generic support; others offer no preparation at all. Since September, 1997, we
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::7e1f2805938877a913044ab110d2d854
http://hdl.handle.net/20.500.11769/40197
http://hdl.handle.net/20.500.11769/40197
