Detalhe da pesquisa
1.
Genetic events associated with venetoclax resistance in CLL identified by whole-exome sequencing of patient samples.
Blood
; 142(5): 421-433, 2023 08 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37146250
2.
Reduced telomere length in amniocytes: an early biomarker of abnormal fetal development?
Hum Mol Genet
; 31(16): 2669-2677, 2022 08 23.
Artigo
em Inglês
| MEDLINE | ID: mdl-35244708
3.
Faster clinical decisions in B-cell acute lymphoblastic leukaemia: A single flow cytometric 12-colour tube improves diagnosis and minimal residual disease follow-up.
Br J Haematol
; 204(5): 1872-1881, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38432068
4.
Real-world outcomes following venetoclax therapy in patients with chronic lymphocytic leukemia or Richter syndrome: a FILO study of the French compassionate use cohort.
Ann Hematol
; 100(4): 987-993, 2021 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-33495922
5.
Poor prognosis of chromosome 7 clonal aberrations in Philadelphia-negative metaphases and relevance of potential underlying myelodysplastic features in chronic myeloid leukemia.
Haematologica
; 104(6): 1150-1155, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30573507
6.
The t(X;20)(q13;q13) translocation is a good prognostic factor in myeloid neoplasms: A report of 25 cases from the Groupe Francophone de Cytogénétique Hématologique.
Am J Hematol
; 2024 Apr 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-38613825
7.
"Double-hit" chronic lymphocytic leukemia: An aggressive subgroup with 17p deletion and 8q24 gain.
Am J Hematol
; 93(3): 375-382, 2018 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-29194741
8.
Presence of multiple recurrent mutations confers poor trial outcome of relapsed/refractory CLL.
Blood
; 126(18): 2110-7, 2015 Oct 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26316624
9.
TP53 mutations at codon 234 are associated with chlorambucil treatment in chronic lymphocytic leukemia.
Am J Hematol
; 97(4): E159-E162, 2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35083778
10.
Clinical and biological characteristics of leukemia cutis in chronic lymphocytic leukemia: A study of the French innovative leukemia organization (FILO).
Am J Hematol
; 96(9): E353-E356, 2021 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34152612
11.
14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma.
Genes Chromosomes Cancer
; 53(8): 657-66, 2014 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-24729385
12.
De novo 2q36.1q36.3 interstitial deletion involving the PAX3 and EPHA4 genes in a fetus with spina bifida and cleft palate.
Birth Defects Res A Clin Mol Teratol
; 100(6): 507-11, 2014 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-24753315
13.
Outcome and impact of post-remission strategy after MIDAM regimen in patients with relapsing or refractory acute myeloid leukemia.
Am J Hematol
; 94(1): E32-E35, 2019 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-30370957
14.
Chromosomal aberrations and their prognostic value in a series of 174 untreated patients with Waldenström's macroglobulinemia.
Haematologica
; 98(4): 649-54, 2013 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-23065509
15.
Cytogenetics in the management of chronic lymphocytic leukemia: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103410, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38039634
16.
Optical Genome Mapping in Routine Cytogenetic Diagnosis of Acute Leukemia.
Cancers (Basel)
; 15(7)2023 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-37046792
17.
Cytogenetics in the management of mature T-cell and NK-cell neoplasms: Guidelines from the Groupe Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103428, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38016421
18.
Cytogenetics in the management of myeloproliferative neoplasms, mastocytosis and myelodysplastic/myeloproliferative neoplasms: Guidelines from the Group Francophone de Cytogénétique Hématologique (GFCH).
Curr Res Transl Med
; 71(4): 103424, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38011761
19.
Feasibility of Optical Genome Mapping from Placental and Umbilical Cord Sampled after Spontaneous or Therapeutic Pregnancy Termination.
Diagnostics (Basel)
; 13(23)2023 Nov 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-38066817
20.
Optical genome mapping for prenatal diagnosis: A prospective study.
Clin Chim Acta
; 551: 117594, 2023 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-37832906