Giarin E - Search Results

1

Comparative sequence analysis of incomplete DJH and TCR gene rearrangements in children with relapses of T-ALL.

Germano G, del Giudice L, Lo Nigro L, Polato K, Giarin E, Paganin M, Basso G. Germano G, et al. Among authors: giarin e. Leukemia. 2005 Sep;19(9):1687-9. doi: 10.1038/sj.leu.2403878. Leukemia. 2005. PMID: 16015384 No abstract available.

2

Clonality profile in relapsed precursor-B-ALL children by GeneScan and sequencing analyses. Consequences on minimal residual disease monitoring.

Germano G, del Giudice L, Palatron S, Giarin E, Cazzaniga G, Biondi A, Basso G. Germano G, et al. Among authors: giarin e. Leukemia. 2003 Aug;17(8):1573-82. doi: 10.1038/sj.leu.2403008. Leukemia. 2003. PMID: 12886245

3

Poor prognosis for P2RY8-CRLF2 fusion but not for CRLF2 over-expression in children with intermediate risk B-cell precursor acute lymphoblastic leukemia.

Palmi C, Vendramini E, Silvestri D, Longinotti G, Frison D, Cario G, Shochat C, Stanulla M, Rossi V, Di Meglio AM, Villa T, Giarin E, Fazio G, Leszl A, Schrappe M, Basso G, Biondi A, Izraeli S, Conter V, Valsecchi MG, Cazzaniga G, Te Kronnie G. Palmi C, et al. Among authors: giarin e. Leukemia. 2012 Oct;26(10):2245-53. doi: 10.1038/leu.2012.101. Epub 2012 Apr 9. Leukemia. 2012. PMID: 22484421

4

Prognostic value of minimal residual disease measured by flow-cytometry in two cohorts of infants with acute lymphoblastic leukemia treated according to either MLL-Baby or Interfant protocols.

Popov A, Buldini B, De Lorenzo P, Disarò S, Verzhbitskaya T, Movchan L, Giarin E, Shorikov E, Di Meglio A, Tsaur G, Parasole R, Miakova N, Boichenko E, Kondratchik K, Aleinikova O, Karachunskiy A, Roumiantsev A, Locatelli F, Biondi A, Pieters R, Valsecchi MG, Fechina L, Basso G. Popov A, et al. Among authors: giarin e. Leukemia. 2020 Nov;34(11):3042-3046. doi: 10.1038/s41375-020-0912-z. Epub 2020 Jun 12. Leukemia. 2020. PMID: 32533093 No abstract available.

5

Identification of immunophenotypic signatures by clustering analysis in pediatric patients with Philadelphia chromosome-positive acute lymphoblastic leukemia.

Buldini B, Zangrando A, Michielotto B, Veltroni M, Giarin E, Tosato F, Cazzaniga G, Biondi A, Basso G. Buldini B, et al. Among authors: giarin e. Am J Hematol. 2010 Feb;85(2):138-41. doi: 10.1002/ajh.21595. Am J Hematol. 2010. PMID: 20095033 Free article. No abstract available.

6

Altered mRNA expression of PAX5 is a common event in acute lymphoblastic leukaemia.

Santoro A, Bica MG, Dagnino L, Agueli C, Salemi D, Cannella S, Veltroni M, Cetica V, Giarin E, Fabbiano F, Basso G, Arico M. Santoro A, et al. Among authors: giarin e. Br J Haematol. 2009 Sep;146(6):686-9. doi: 10.1111/j.1365-2141.2009.07815.x. Epub 2009 Jul 13. Br J Haematol. 2009. PMID: 19604238 Free article. No abstract available.

7

Glutathione S-transferase homozygous deletions and relapse in childhood acute lymphoblastic leukemia: a novel study design in a large Italian AIEOP cohort.

Franca R, Rebora P, Basso G, Biondi A, Cazzaniga G, Crovella S, Decorti G, Fagioli F, Giarin E, Locatelli F, Poggi V, Valsecchi MG, Rabusin M. Franca R, et al. Among authors: giarin e. Pharmacogenomics. 2012 Dec;13(16):1905-16. doi: 10.2217/pgs.12.169. Pharmacogenomics. 2012. PMID: 23215883

8

Pre- and post-transplant minimal residual disease predicts relapse occurrence in children with acute lymphoblastic leukaemia.

Lovisa F, Zecca M, Rossi B, Campeggio M, Magrin E, Giarin E, Buldini B, Songia S, Cazzaniga G, Mina T, Acquafredda G, Quarello P, Locatelli F, Fagioli F, Basso G. Lovisa F, et al. Among authors: giarin e. Br J Haematol. 2018 Mar;180(5):680-693. doi: 10.1111/bjh.15086. Epub 2018 Jan 23. Br J Haematol. 2018. PMID: 29359790 Free article.

9

Nucleophosmin mutations in childhood acute myelogenous leukemia with normal karyotype.

Cazzaniga G, Dell'Oro MG, Mecucci C, Giarin E, Masetti R, Rossi V, Locatelli F, Martelli MF, Basso G, Pession A, Biondi A, Falini B. Cazzaniga G, et al. Among authors: giarin e. Blood. 2005 Aug 15;106(4):1419-22. doi: 10.1182/blood-2005-03-0899. Epub 2005 May 3. Blood. 2005. PMID: 15870172 Free article.

10

Frequent cases of RAS-mutated Down syndrome acute lymphoblastic leukaemia lack JAK2 mutations.

Nikolaev SI, Garieri M, Santoni F, Falconnet E, Ribaux P, Guipponi M, Murray A, Groet J, Giarin E, Basso G, Nizetic D, Antonarakis SE. Nikolaev SI, et al. Among authors: giarin e. Nat Commun. 2014 Aug 8;5:4654. doi: 10.1038/ncomms5654. Nat Commun. 2014. PMID: 25105841 Free PMC article.

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