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687 results

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Page 1
Frequency and prognostic implications of JAK 1-3 aberrations in Down syndrome acute lymphoblastic and myeloid leukemia.
Blink M, Buitenkamp TD, van den Heuvel-Eibrink MM, Danen-van Oorschot AA, de Haas V, Reinhardt D, Klusmann JH, Zimmermann M, Devidas M, Carroll AJ, Basso G, Pession A, Hasle H, Pieters R, Rabin KR, Izraeli S, Zwaan CM. Blink M, et al. Among authors: pession a. Leukemia. 2011 Aug;25(8):1365-8. doi: 10.1038/leu.2011.86. Epub 2011 May 3. Leukemia. 2011. PMID: 21537335 No abstract available.
Genomic profiling in Down syndrome acute lymphoblastic leukemia identifies histone gene deletions associated with altered methylation profiles.
Loudin MG, Wang J, Leung HC, Gurusiddappa S, Meyer J, Condos G, Morrison D, Tsimelzon A, Devidas M, Heerema NA, Carroll AJ, Plon SE, Hunger SP, Basso G, Pession A, Bhojwani D, Carroll WL, Rabin KR. Loudin MG, et al. Among authors: pession a. Leukemia. 2011 Oct;25(10):1555-63. doi: 10.1038/leu.2011.128. Epub 2011 Jun 7. Leukemia. 2011. PMID: 21647151 Free PMC article.
JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia.
Zecca M, Bergamaschi G, Kratz C, Bergsträsser E, Danesino C, De Filippi P, Hasle H, Lisini D, Locatelli F, Pession A, Sainati L, Starý J, Trebo M, van den Heuvel-Eibrink M, Wójcik D, Niemeyer CM. Zecca M, et al. Among authors: pession a. Leukemia. 2007 Feb;21(2):367-9. doi: 10.1038/sj.leu.2404484. Epub 2006 Dec 7. Leukemia. 2007. PMID: 17151700 No abstract available.
Clinical features of childhood acute myeloid leukaemia with specific gene rearrangements.
Frascella E, Rondelli R, Pigazzi M, Zampieron C, Fagioli F, Favre C, Lippi AA, Locatelli F, Luciani M, Menna G, Micalizzi C, Rizzari C, Testi AM, Pession A, Basso G. Frascella E, et al. Among authors: pession a. Leukemia. 2004 Aug;18(8):1427-9. doi: 10.1038/sj.leu.2403410. Leukemia. 2004. PMID: 15201852 No abstract available.
Long-term results of the Italian Association of Pediatric Hematology and Oncology (AIEOP) Studies 82, 87, 88, 91 and 95 for childhood acute lymphoblastic leukemia.
Conter V, Aricò M, Basso G, Biondi A, Barisone E, Messina C, Parasole R, De Rossi G, Locatelli F, Pession A, Santoro N, Micalizzi C, Citterio M, Rizzari C, Silvestri D, Rondelli R, Lo Nigro L, Ziino O, Testi AM, Masera G, Valsecchi MG; Associazione Italiana di Ematologia ed Oncologia Pediatrica. Conter V, et al. Among authors: pession a. Leukemia. 2010 Feb;24(2):255-64. doi: 10.1038/leu.2009.250. Epub 2009 Dec 17. Leukemia. 2010. PMID: 20016536 Clinical Trial.
Low prevalence of IDH1 gene mutation in childhood AML in Italy.
Pigazzi M, Ferrari G, Masetti R, Falini B, Martinolli F, Basso G, Biondi A, Pession A, Cazzaniga G. Pigazzi M, et al. Among authors: pession a. Leukemia. 2011 Jan;25(1):173-4. doi: 10.1038/leu.2010.229. Epub 2010 Oct 14. Leukemia. 2011. PMID: 20944672 No abstract available.
Detection of PICALM-MLLT10 (CALM-AF10) and outcome in children with T-lineage acute lymphoblastic leukemia.
Lo Nigro L, Mirabile E, Tumino M, Caserta C, Cazzaniga G, Rizzari C, Silvestri D, Buldini B, Barisone E, Casale F, Luciani M, Locatelli F, Messina C, Micalizzi C, Pession A, Parasole R, Santoro N, Masera G, Basso G, Aricò M, Valsecchi M, Biondi A, Conter V; AIEOP—Scientific Committee of ALL. Lo Nigro L, et al. Among authors: pession a. Leukemia. 2013 Dec;27(12):2419-21. doi: 10.1038/leu.2013.149. Epub 2013 May 14. Leukemia. 2013. PMID: 23670296 No abstract available.
687 results