Search details
1.
UBTF-internal tandem duplication as a novel poor prognostic factor in pediatric acute myeloid leukemia.
Genes Chromosomes Cancer
; 62(4): 202-209, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36448876
2.
TP53 and RB1 alterations characterize poor prognostic subgroups in pediatric acute myeloid leukemia.
Genes Chromosomes Cancer
; 62(7): 412-422, 2023 07.
Article
in English
| MEDLINE | ID: mdl-37102302
3.
Therapeutic options for CTLA-4 insufficiency.
J Allergy Clin Immunol
; 149(2): 736-746, 2022 02.
Article
in English
| MEDLINE | ID: mdl-34111452
4.
Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia.
Haematologica
; 107(3): 583-592, 2022 03 01.
Article
in English
| MEDLINE | ID: mdl-33730843
5.
Patients aged less than 3 years with acute myeloid leukaemia characterize a molecularly and clinically distinct subgroup.
Br J Haematol
; 188(4): 528-539, 2020 02.
Article
in English
| MEDLINE | ID: mdl-31612466
6.
Clinical features and prognostic impact of PRDM16 expression in adult acute myeloid leukemia.
Genes Chromosomes Cancer
; 56(11): 800-809, 2017 11.
Article
in English
| MEDLINE | ID: mdl-28710806
7.
ASXL2 mutations are frequently found in pediatric AML patients with t(8;21)/ RUNX1-RUNX1T1 and associated with a better prognosis.
Genes Chromosomes Cancer
; 56(5): 382-393, 2017 05.
Article
in English
| MEDLINE | ID: mdl-28063196
8.
High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3-ITD, KMT2A-PTD, and NUP98-NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial.
Br J Haematol
; 172(4): 581-91, 2016 Feb.
Article
in English
| MEDLINE | ID: mdl-26684393
9.
CSF3R and CALR mutations in paediatric myeloid disorders and the association of CSF3R mutations with translocations, including t(8; 21).
Br J Haematol
; 170(3): 391-7, 2015 Aug.
Article
in English
| MEDLINE | ID: mdl-25858548
10.
RUNX1 mutations in pediatric acute myeloid leukemia are associated with distinct genetic features and an inferior prognosis.
Blood
; 131(20): 2266-2270, 2018 05 17.
Article
in English
| MEDLINE | ID: mdl-29540347
11.
Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia.
Blood
; 120(7): 1485-8, 2012 Aug 16.
Article
in English
| MEDLINE | ID: mdl-22753870
12.
NUP98-NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia.
Genes Chromosomes Cancer
; 52(7): 683-93, 2013 Jul.
Article
in English
| MEDLINE | ID: mdl-23630019
13.
Genome-wide DNA methylation analysis in pediatric acute myeloid leukemia.
Blood Adv
; 6(11): 3207-3219, 2022 06 14.
Article
in English
| MEDLINE | ID: mdl-35008106
14.
Clinical features of 35 Down syndrome patients with transient abnormal myelopoiesis at a single institution.
Int J Hematol
; 113(5): 662-667, 2021 May.
Article
in English
| MEDLINE | ID: mdl-33394336
15.
Quantitative assessment of PTPN11 or RAS mutations at the neonatal period and during the clinical course in patients with juvenile myelomonocytic leukaemia.
Br J Haematol
; 148(4): 593-9, 2010 Feb.
Article
in English
| MEDLINE | ID: mdl-19874312
16.
SETBP1 mutations in juvenile myelomonocytic leukaemia and myelodysplastic syndrome but not in paediatric acute myeloid leukaemia.
Br J Haematol
; 164(1): 156-9, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24117422
17.
Mutations of the GATA2 and CEBPA genes in paediatric acute myeloid leukaemia.
Br J Haematol
; 164(1): 142-5, 2014 Jan.
Article
in English
| MEDLINE | ID: mdl-24033149
18.
Correction to: Factors predicting the recurrence of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children after treatment using the HLH-2004 protocol.
Int J Hematol
; 109(5): 629, 2019 May.
Article
in English
| MEDLINE | ID: mdl-30977106
19.
Factors predicting the recurrence of Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis in children after treatment using the HLH-2004 protocol.
Int J Hematol
; 109(5): 612-617, 2019 May.
Article
in English
| MEDLINE | ID: mdl-30788725
20.
Transcriptome analysis offers a comprehensive illustration of the genetic background of pediatric acute myeloid leukemia.
Blood Adv
; 3(20): 3157-3169, 2019 10 22.
Article
in English
| MEDLINE | ID: mdl-31648321