Detalhe da pesquisa
1.
Congenital Hemolytic Anemia Because of Glucose Phosphate Isomerase Deficiency: Identification of 2 Novel Missense Mutations in the GPI Gene.
J Pediatr Hematol Oncol
; 42(7): e696-e697, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-31415279
2.
A molecular study on the role of alpha-hemoglobin-stabilizing protein in hemoglobin H disease.
Ann Hematol
; 96(6): 1005-1014, 2017 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-28337528
3.
Spontaneous resolution of refractory cytopenia of childhood with monosomy 7 in an infant without an identifiable genetic cause.
Pediatr Blood Cancer
; 69(10): e29654, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35389555
4.
Curative Stem Cell Transplantation for Severe Hb H Disease Manifesting From Early Infancy: Phenotypic and Genotypic Analyses.
Hemoglobin
; 40(1): 70-3, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26575104
5.
Epigenetic dysregulation of leukaemic HOX code in MLL-rearranged leukaemia mouse model.
J Pathol
; 232(1): 65-74, 2014 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-24122813
6.
Novel point mutation of the α2-globin gene (HBA2) and a rare 2.4 kb deletion of the α1-globin gene (HBA1), identified in two chinese patients with Hb H disease.
Hemoglobin
; 38(3): 213-5, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-24826793
7.
Diagnosis and prevention of thalassemia.
Crit Rev Clin Lab Sci
; 50(6): 125-41, 2013 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-24295057
8.
Epigenetic inactivation of the MIR34B/C in multiple myeloma.
Blood
; 118(22): 5901-4, 2011 Nov 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-21976676
9.
Establishment of a bortezomib-resistant Chinese human multiple myeloma cell line: MMLAL.
Cancer Cell Int
; 13(1): 122, 2013 Dec 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-24330858
10.
Central diabetes insipidus: an unusual complication in a child with juvenile myelomonocytic leukemia and monosomy 7.
J Pediatr Hematol Oncol
; 35(2): e84-7, 2013 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22858568
11.
CD44 activation in mature B-cell malignancies by a novel recurrent IGH translocation.
Blood
; 115(12): 2458-61, 2010 Mar 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-20093404
12.
NGS4THAL, a One-Stop Molecular Diagnosis and Carrier Screening Tool for Thalassemia and Other Hemoglobinopathies by Next-Generation Sequencing.
J Mol Diagn
; 24(10): 1089-1099, 2022 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-35868510
13.
Pharmacogenomic Profiling of Pediatric Acute Myeloid Leukemia to Identify Therapeutic Vulnerabilities and Inform Functional Precision Medicine.
Blood Cancer Discov
; 3(6): 516-535, 2022 11 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-35960210
14.
Epigenetic silencing of MIR203 in multiple myeloma.
Br J Haematol
; 154(5): 569-78, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-21707582
15.
Hb A2 Hong Kong - A novel δ-globin variant in a Chinese family masks the diagnosis of ß-thalassemia trait.
Hemoglobin
; 35(2): 162-5, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21417575
16.
Alpha thalassemia trait masquerading as hemoglobin H disease due to co-existing primary myelofibrosis.
Ann Hematol
; 94(5): 875-7, 2015 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-25465234
17.
The significance of dyserythropoiesis.
Br J Haematol
; 164(3): 313, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24117396
18.
Functional alterations of Lin-CD34+CD38+ cells in chronic myelomonocytic leukemia and on progression to acute leukemia.
Leuk Res
; 32(9): 1374-81, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18372040
19.
Pure red cell aplasia associated with CD20+ myeloma: complete remission with rituximab.
Ann Hematol
; 92(10): 1425-6, 2013 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-23494205
20.
A dual colour dual fusion fluorescence in situ hybridisation study on the genesis of complex variant translocations in chronic myelogenous leukaemia.
Oncol Rep
; 19(5): 1181-4, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18425374