Zobrazeno 1 - 10
of 368
pro vyhledávání: '"A. Cantù Rajnoldi"'
Autor:
Sainty, Danielle *, Liso, Vincenzo, Cantù-Rajnoldi, Angelo, Head, David, Mozziconacci, Marie-Joëlle, Arnoulet, Christine, Benattar, Laurence, Fenu, Susanna, Mancini, Marco, Duchayne, Eliane, Mahon, François-Xavier, Gutierrez, Norma, Birg, Françoise, Biondi, Andrea, Grimwade, David, Lafage-Pochitaloff, Marina, Hagemeijer, Anne, Flandrin, Georges
Publikováno v:
In Blood 15 August 2000 96(4):1287-1296
Autor:
C. Vegni, U. Nicolini, A. Zanella, P. Faccini, Davide Soligo, G. Gornati, U. Conter, Cantù-Rajnoldi A
Publikováno v:
British Journal of Haematology. 96:530-533
We describe a case of congenital dyserythropoietic anaemia (CDA) presenting at week 20 of pregnancy with hydrops fetalis and very severe anaemia. Fetal blood examination showed marked erythroblastosis with morphologic alterations while the basic haem
Autor:
Lucas, Bryony J.1 (AUTHOR), Connors, Jeremy S.2 (AUTHOR), Wang, Heping3 (AUTHOR), Conneely, Shannon1 (AUTHOR), Cuglievan, Branko2,4 (AUTHOR), Garcia, Miriam B.2,4 (AUTHOR) mbgarcia@mdanderson.org, Rau, Rachel E.5 (AUTHOR) mbgarcia@mdanderson.org
Publikováno v:
Cancers. Aug2024, Vol. 16 Issue 15, p2749. 16p.
Autor:
Hasle, H., Aricò, M., Basso, G., Biondi, A., Cantù-Rajnoldi, A., Creuzig, U., Fenu, S., Fonatsch, C., Haas, O.A., Harbott, J., Kardos, G., Kerndrup, G. m.fl.
Publikováno v:
Hasle, H, Aricò, M, Basso, G, Biondi, A, Cantù-Rajnoldi, A, Creuzig, U, Fenu, S, Fonatsch, C, Haas, O A, Harbott, J, Kardos, G & Kerndrup, G M F 1999, ' Myelodysplastic syndrome, juvenile myelomonocytic leukemia, and acute myeloid leukemia associated with complete or partial monosomy7 : An EWOG-MDS study of 100 children ', Leukemia, vol. 3, pp. 376-85 .
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3062::b36593f6f77252ede3b3ae20ab596db2
https://portal.findresearcher.sdu.dk/da/publications/361f5ca0-6fcf-11db-81a9-000ea68e967b
https://portal.findresearcher.sdu.dk/da/publications/361f5ca0-6fcf-11db-81a9-000ea68e967b
Autor:
Andrea Biondi, G Giudici, L Romitti, A. Cantù Rajnoldi, Valentino Conter, M. R. Rossi, Carmelo Rizzari, Anna Locasciulli, Momcilo Jankovic, Attilio Rovelli
Publikováno v:
Journal of Clinical Oncology. 10:1413-1418
PURPOSE The microgranular variant (M3v) of acute promyelocytic leukemia (APL) rarely has been reported in a pediatric series of acute nonlymphoblastic leukemia (AnLL). We reviewed the clinical and biologic features of childhood M3v cases in our AnLL
Autor:
Giovanni Giudici, P D'Angelo, L. Crosti, Cantù-Rajnoldi A, Andrea Biondi, Carmelo Rizzari, Marina Castagni, Rosamaria Mura
Publikováno v:
Pediatric Hematology and Oncology. 9:281-288
(1992). Lineage Switch in a Childhood T-Cell Acute Lymphoblastic Leukemia. Pediatric Hematology and Oncology: Vol. 9, No. 3, pp. 281-288.
Autor:
Francesco Lo Coco, Susanna Fenu, Andrea Biondi, D. Pasqualetti, Cantù-Rajnoldi A, Maria Concetta Petti, Franco Mandelli, Mauro Nanni, Giuseppe Avvisati, Daniela Diverio, Myriam Alcalay, P P Pandolfi, Giulio De Rossi, M. Frontani
Publikováno v:
British Journal of Haematology. 78:494-499
We have used genomic probes which specifically recognize DNA rearrangements of the RAR-alpha locus on chromosome 17q21 in patients with acute promyelocytic leukaemia (APL) and acute myeloid leukaemia (AML) subtypes. Molecular data were examined in co
Autor:
Carmelo Rizzari, Angelo Cantù Rajnoldi, Giuseppe Masera, Momcilo Jankovic, Valentino Confer, Cornelio Uderzo, Anna Cappellini
Publikováno v:
Pediatric Hematology and Oncology. 8:263-267
Autor:
Adriana Balduzzi, Lilia Corral, Giuseppe Gaipa, G Germano, Andrea Biondi, Cantù-Rajnoldi A, Giovanni Giudici
Publikováno v:
Leukemia. 13:2114-2116
Autor:
Giuseppe Avvisati, Daniela Diverio, Maria Grazia Cocito, Luigi Del Vecchio, Antonio Tabilio, Cesare Guglielmi, Susanna Fenu, Maria Paola Martelli, Giuseppe Basso, M. L. Vegna, Cantù-Rajnoldi A, Francesco Lo Coco, Andrea Biondi
Publikováno v:
British journal of haematology. 102(4)
Acute promyelocytic leukaemia (APL), characterized by a specific PML-RARalpha fusion gene resulting from translocation t(15;17) and by a high response rate to differentiation therapy with all-trans retinoic acid, presents clinical (varying WBC counts