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scopus: 6603911444

Sainati, L.

(Laura Sainati)


karyotype patient mutation leukemia children aberration blood myeloid leukemia monosomal karyotype study myeloid university group cytogenetic monosomal analysis v 617f mutation department childhood myelomonocytic leukemia myelodysplastic syndrome monosomy hospital hematology diagnosis oncology ptpn 11 npm 1 mutations table 5- year os 3 clonal aberrations disease probability survival germany erasmus mc myelodysplastic syndrome myelomonocytic niemeyer cm niemeyer clonal myelodysplastic syndromes hematology /oncology university prognosis finition 3 chromosomal aberrations adult article event myeloproliferative factor hematopoietic autosomal monosomy identi fied prognostic outcome monosomy 7 kinase range jak 2 disorder clonal evolution abnormality erasmu presence result development autosomal signi childhood mds blood 2 autosomal monosomies american society activation italy ful fill growth creutzig ras mutations â 109/ l




2 Most Recent Publications

Complex karyotype newly defined: The strongest prognostic factor in advanced childhood myelodysplastic syndrome (Article)
Göhring, G. Michalova, K. Stary, J. Trebo, M. Heuvel-Eibrink, M.M. van den Zecca, M. Wering, E.R. van Fischer, A.M. Noellke, P. Strahm, B. Locatelli, F. Niemeyer, C.M. Beverloo, H.B. Schlegelberger, B. Betts, D. Harbott, J. Haas, O.A. Kerndrup, G. Sainati, L. Bergstraesser, E. Hasle, H.
2010-11-11
JAK2 V617F mutation is a rare event in juvenile myelomonocytic leukemia [9] (Article)
Zecca, M. Bergamaschi, G. Sainati, L. Stary, J. Trebo, M. Heuvel-Eibrink, M.M. van den Wojcik, D. Niemeyer, C.M. Kratz, C.P. Bergsträsser, E. Danesino, C. Filippi, P. de Hasle, H. Lisini, D. Locatelli, F. Pession, A.
2007-02-01