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1.
Classical meets malignant hematology: a case of acquired εγδß-thalassemia in clonal hematopoiesis.
Haematologica;
2024 Mar 14.
Artículo
en Inglés
| MEDLINE | ID: mdl-38497167
2.
Identification of prognostic parameters in CLL with no abnormalities detected by chromosome banding and FISH analyses.
Br J Haematol;
183(1): 47-59, 2018 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30022491
3.
TP53 mutations occur in 15.7% of ALL and are associated with MYC-rearrangement, low hypodiploidy, and a poor prognosis.
Blood;
124(2): 251-8, 2014 Jul 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-24829203
4.
Acute lymphoblastic leukemia with low hypodiploid/near triploid karyotype is a specific clinical entity and exhibits a very high TP53 mutation frequency of 93%.
Genes Chromosomes Cancer;
53(6): 524-36, 2014 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-24619868
5.
The molecular profile of adult T-cell acute lymphoblastic leukemia: mutations in RUNX1 and DNMT3A are associated with poor prognosis in T-ALL.
Genes Chromosomes Cancer;
52(4): 410-22, 2013 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-23341344
6.
CEBPA double-mutated acute myeloid leukaemia harbours concomitant molecular mutations in 76·8% of cases with TET2 and GATA2 alterations impacting prognosis.
Br J Haematol;
161(5): 649-658, 2013 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-23521373
7.
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
8.
Accumulation of adverse prognostic markers worsens prognosis in chronic lymphocytic leukaemia.
Br J Haematol;
168(1): 153-6, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25135300
9.
Refractory anemia with ring sideroblasts and marked thrombocytosis cases harbor mutations in SF3B1 or other spliceosome genes accompanied by JAK2V617F and ASXL1 mutations.
Haematologica;
100(4): e125-7, 2015 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-25527566
10.
Robustness of amplicon deep sequencing underlines its utility in clinical applications.
J Mol Diagn;
15(4): 473-84, 2013 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-23680131
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