Detalhe da pesquisa
1.
Topical therapy and skin care for transplant-associated atopic dermatitis in children and adolescents.
Pediatr Transplant
; 28(1): e14653, 2024 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-37990976
2.
Clinical conditions and risk factors for inhibitor-development in patients with haemophilia: A decade-long prospective cohort study in Japan, J-HIS2 (Japan Hemophilia Inhibitor Study 2).
Haemophilia
; 28(5): 745-759, 2022 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-35689832
3.
Mutations in MECOM, Encoding Oncoprotein EVI1, Cause Radioulnar Synostosis with Amegakaryocytic Thrombocytopenia.
Am J Hum Genet
; 97(6): 848-54, 2015 Dec 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-26581901
4.
Amelioration of inflammation and tissue damage in sickle cell model mice by Nrf2 activation.
Proc Natl Acad Sci U S A
; 112(39): 12169-74, 2015 Sep 29.
Artigo
em Inglês
| MEDLINE | ID: mdl-26371321
5.
Onset of Hemophagocytic Lymphohistiocytosis during Piperacillin-Tazobactam Therapy in Three Children with Acute Focal Bacterial Nephritis.
Tohoku J Exp Med
; 245(1): 55-59, 2018 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-29798969
6.
Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets.
Pediatr Blood Cancer
; 62(12): 2082-8, 2015 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-26175287
7.
Pharmacokinetics, efficacy, and safety of caspofungin in Japanese pediatric patients with invasive candidiasis and invasive aspergillosis.
J Infect Chemother
; 21(6): 421-6, 2015 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-25701307
8.
Gene alterations involving the CRLF2-JAK pathway and recurrent gene deletions in Down syndrome-associated acute lymphoblastic leukemia in Japan.
Genes Chromosomes Cancer
; 53(11): 902-10, 2014 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044358
9.
TUBB1 mutation disrupting microtubule assembly impairs proplatelet formation and results in congenital macrothrombocytopenia.
Eur J Haematol
; 92(4): 276-82, 2014 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-24344610
10.
Selective expansion of donor-derived regulatory T cells after allogeneic bone marrow transplantation in a patient with IPEX syndrome.
Pediatr Transplant
; 18(1): E25-30, 2014 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-24224516
11.
Successful treatment of ETV6-NTRK3 fusion gene-negative infantile fibrosarcoma with metastatic lesion resistant to VAC chemotherapy.
Pediatr Int
; 60(11): 1045-1046, 2018 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30536487
12.
Reduced-intensity conditioning is effective for allogeneic hematopoietic stem cell transplantation in infants with MECOM-associated syndrome.
Int J Hematol
; 117(4): 598-606, 2023 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-36515795
13.
Splenectomy resolves hemolytic anemia caused by adenylate kinase deficiency.
Pediatr Int
; 59(2): 228-230, 2017 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211224
14.
Fatigue in survivors of childhood acute lymphoblastic and myeloid leukemia in Japan.
Pediatr Int
; 54(2): 272-6, 2012 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-22136577
15.
Favorable prognosis of vaccine-associated immune thrombocytopenia in children is correlated with young age at vaccination: Retrospective survey of a nationwide disease registry.
Int J Hematol
; 115(1): 114-122, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34626332
16.
Identification of FOXP3-negative regulatory T-like (CD4(+)CD25(+)CD127(low)) cells in patients with immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.
Clin Immunol
; 141(1): 111-20, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21802372
17.
Prospective study of a therapeutic regimen with all-trans retinoic acid and anthracyclines in combination of cytarabine in children with acute promyelocytic leukaemia: the Japanese childhood acute myeloid leukaemia cooperative study.
Br J Haematol
; 152(1): 89-98, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20735397
18.
Pneumococcal Serotype-specific Opsonophagocytic Activity in Interleukin-1 Receptor-associated Kinase 4-deficient Patients.
Pediatr Infect Dis J
; 40(5): 460-463, 2021 05 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-33470775
19.
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies.
J Hum Genet
; 55(12): 801-9, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20882035
20.
A 9-month-old infant with acquired idiopathic thrombotic thrombocytopenic purpura caused by inhibitory IgG-autoantibody to ADAMTS13.
Pediatr Hematol Oncol
; 27(1): 53-8, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20121555