Detalhe da pesquisa
1.
Two Aldehyde Clearance Systems Are Essential to Prevent Lethal Formaldehyde Accumulation in Mice and Humans.
Mol Cell
; 80(6): 996-1012.e9, 2020 12 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33147438
2.
Landscape of driver mutations and their clinical effects on Down syndrome-related myeloid neoplasms.
Blood
; 2024 Mar 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-38513239
3.
Scoring system for diagnosis and pretreatment risk assessment of neuroblastoma using urinary biomarker combinations.
Cancer Sci
; 115(5): 1634-1645, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38411285
4.
Single-Cell Transcriptomic Analysis of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis.
J Clin Immunol
; 44(4): 103, 2024 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-38642164
5.
A retrospective analysis of gene fusions and treatment outcomes in pediatric acute megakaryoblastic leukemia without Down syndrome.
Haematologica
; 2024 Feb 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38299674
6.
Noonan Syndrome-related Myeloproliferative Disorder Occurring in the Neonatal Period: Case Report and Literature Review.
J Pediatr Hematol Oncol
; 46(2): e176-e179, 2024 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-38132703
7.
Comparison of Whole Blood and Plasma for Monitoring Cytomegalovirus and Epstein-Barr Virus.
New Microbiol
; 47(1): 52-59, 2024 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-38700884
8.
Haematopoietic cell transplantation for children with acute megakaryoblastic leukaemia without Down syndrome.
Br J Haematol
; 201(4): 747-756, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36786154
9.
A Japanese retrospective study of non-tuberculous mycobacterial infection in children, adolescents, and young adult patients with hematologic-oncologic diseases.
Haematologica
; 2023 Oct 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-37881854
10.
A nationwide survey of late effects in survivors of juvenile myelomonocytic leukemia in Japan.
Pediatr Blood Cancer
; 70(2): e30126, 2023 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-36495260
11.
Juvenile Hemochromatosis With Non-transfused Hemolytic Anemia Caused by a De Novo PIEZO1 Gene Mutation.
J Pediatr Hematol Oncol
; 45(4): e510-e513, 2023 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-36898020
12.
Prospective validation of the provisional entity of refractory cytopenia of childhood, proposed by the World Health Organization.
Br J Haematol
; 196(4): 1031-1039, 2022 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-34729770
13.
TREC/KREC Newborn Screening followed by Next-Generation Sequencing for Severe Combined Immunodeficiency in Japan.
J Clin Immunol
; 42(8): 1696-1707, 2022 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-35902420
14.
Genetic Study of Fanconi Anemia in Infancy Revealed FANCI Mutations and Defective ALDH2 Variant: A Case Report.
J Pediatr Hematol Oncol
; 44(2): e438-e441, 2022 Mar 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-34310468
15.
Difficulties in diagnosing Malassezia furfur bloodstream infection and possibility of spontaneous resolution in a patient undergoing chemotherapy for neuroblastoma: A case report.
J Infect Chemother
; 28(7): 987-990, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35279379
16.
Microsatellite instability-high is rare events in refractory pediatric solid tumors.
Pediatr Hematol Oncol
; 39(5): 468-474, 2022 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-34964684
17.
Successful treatment of a novel type I interferonopathy due to a de novo PSMB9 gene mutation with a Janus kinase inhibitor.
J Allergy Clin Immunol
; 148(2): 639-644, 2021 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-33727065
18.
[A Case of Second Primary Small Cell Lung Carcinoma after Radiotherapy for Breast Cancer].
Gan To Kagaku Ryoho
; 49(12): 1361-1364, 2022 Dec.
Artigo
em Japonês
| MEDLINE | ID: mdl-36539250
19.
Relationship between plasma rabbit anti-thymocyte globulin concentration and immunosuppressive therapy response in patients with severe aplastic anemia.
Eur J Haematol
; 107(2): 255-264, 2021 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-33949001
20.
Biallelic VPS35L pathogenic variants cause 3C/Ritscher-Schinzel-like syndrome through dysfunction of retriever complex.
J Med Genet
; 57(4): 245-253, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31712251