Detalles de la búsqueda
1.
Profiling of somatic mutations in acute myeloid leukemia with FLT3-ITD at diagnosis and relapse.
Blood
; 126(22): 2491-501, 2015 Nov 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-26438511
2.
Gain of chromosome 21 or amplification of chromosome arm 21q is one mechanism for increased ERG expression in acute myeloid leukemia.
Genes Chromosomes Cancer
; 55(2): 148-57, 2016 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-26542308
3.
Changes in cytogenetics and molecular genetics in acute myeloid leukemia from childhood to adult age groups.
Cancer
; 122(24): 3821-3830, 2016 Dec 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-27529519
4.
Feasibility of BAALC gene expression for detection of minimal residual disease and risk stratification in normal karyotype acute myeloid leukaemia.
Br J Haematol
; 175(5): 904-916, 2016 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-27662611
5.
BRCC3 mutations in myeloid neoplasms.
Haematologica
; 100(8): 1051-7, 2015 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-26001790
6.
Evaluation of IDH1G105 polymorphism as prognostic marker in intermediate-risk AML.
Ann Hematol
; 94(12): 1991-2001, 2015 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-26351014
7.
Flow cytometric identification of 76 patients with biclonal disease among 5523 patients with chronic lymphocytic leukaemia (B-CLL) and its genetic characterization.
Br J Haematol
; 164(4): 565-9, 2014 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-24236747
8.
Relapse kinetics in acute myeloid leukaemias with MLL translocations or partial tandem duplications within the MLL gene.
Br J Haematol
; 165(5): 618-28, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24611505
9.
Investigation of 305 patients with myelodysplastic syndromes and 20q deletion for associated cytogenetic and molecular genetic lesions and their prognostic impact.
Br J Haematol
; 164(6): 822-33, 2014 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-24372512
10.
Multilineage dysplasia does not influence prognosis in CEBPA-mutated AML, supporting the WHO proposal to classify these patients as a unique entity.
Blood
; 119(20): 4719-22, 2012 May 17.
Artículo
en Inglés
| MEDLINE | ID: mdl-22442349
11.
Prognostic value of monosomal karyotype in comparison to complex aberrant karyotype in acute myeloid leukemia: a study on 824 cases with aberrant karyotype.
Blood
; 119(9): 2122-5, 2012 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-22207733
12.
SRSF2 mutations in 275 cases with chronic myelomonocytic leukemia (CMML).
Blood
; 120(15): 3080-8, 2012 Oct 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-22919025
13.
RUNX1 mutations are frequent in de novo AML with noncomplex karyotype and confer an unfavorable prognosis.
Blood
; 117(8): 2348-57, 2011 Feb 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-21148331
14.
Serial assessment of suspected myelodysplastic syndromes: significance of flow cytometric findings validated by cytomorphology, cytogenetics, and molecular genetics.
Haematologica
; 98(2): 201-7, 2013 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-22929975
15.
Diversity of the juxtamembrane and TKD1 mutations (exons 13-15) in the FLT3 gene with regards to mutant load, sequence, length, localization, and correlation with biological data.
Genes Chromosomes Cancer
; 51(10): 910-24, 2012 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-22674490
16.
ETV6 rearrangements are recurrent in myeloid malignancies and are frequently associated with other genetic events.
Genes Chromosomes Cancer
; 51(4): 328-37, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22162288
17.
Gene expression of BAALC, CDKN1B, ERG, and MN1 adds independent prognostic information to cytogenetics and molecular mutations in adult acute myeloid leukemia.
Genes Chromosomes Cancer
; 51(3): 257-65, 2012 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-22072540
18.
Monoclonal B-cell lymphocytosis is closely related to chronic lymphocytic leukaemia and may be better classified as early-stage CLL.
Br J Haematol
; 157(1): 86-96, 2012 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-22224978
19.
TET2 deletions are a recurrent but rare phenomenon in myeloid malignancies and are frequently accompanied by TET2 mutations on the remaining allele.
Br J Haematol
; 156(1): 67-75, 2012 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-22017486
20.
IDH1 mutations are detected in 6.6% of 1414 AML patients and are associated with intermediate risk karyotype and unfavorable prognosis in adults younger than 60 years and unmutated NPM1 status.
Blood
; 116(25): 5486-96, 2010 Dec 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-20805365