Detalhe da pesquisa
1.
A variant in human AIOLOS impairs adaptive immunity by interfering with IKAROS.
Nat Immunol
; 22(7): 893-903, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-34155405
2.
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
Inglês
| MEDLINE | ID: mdl-38132703
3.
Intracranial residual lesions following early intensification in a patient with T-cell acute lymphoblastic leukemia: a case report.
BMC Pediatr
; 24(1): 304, 2024 May 04.
Artigo
Inglês
| MEDLINE | ID: mdl-38704558
4.
Clinical and Genetic Characterization of Patients with Artemis Deficiency in Japan.
J Clin Immunol
; 43(3): 585-594, 2023 Apr.
Artigo
Inglês
| MEDLINE | ID: mdl-36385359
5.
Cord Blood Transplantation in 2 Infants Presenting Monosomy 7 Clonal Hematopoiesis: SAMD9 / SAMD9L Germline Mutation.
J Pediatr Hematol Oncol
; 45(2): e290-e293, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36730951
6.
Successful TCRαß/CD19-Depleted Hematopoietic Cell Transplantation for a Patient With Artemis Deficiency.
J Pediatr Hematol Oncol
; 45(2): e285-e289, 2023 03 01.
Artigo
Inglês
| MEDLINE | ID: mdl-36757045
7.
Transient immune deficiency accompanied with homozygous CBL rare variant.
Pediatr Int
; 65(1): e15439, 2023 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-36495474
8.
Therapeutic options for CTLA-4 insufficiency.
J Allergy Clin Immunol
; 149(2): 736-746, 2022 02.
Artigo
Inglês
| MEDLINE | ID: mdl-34111452
9.
International retrospective study of allogeneic hematopoietic cell transplantation for activated PI3K-delta syndrome.
J Allergy Clin Immunol
; 149(1): 410-421.e7, 2022 01.
Artigo
Inglês
| MEDLINE | ID: mdl-34033842
10.
Hematopoietic Cell Transplantation for Inborn Errors of Immunity Other than Severe Combined Immunodeficiency in Japan: Retrospective Analysis for 1985-2016.
J Clin Immunol
; 42(3): 529-545, 2022 04.
Artigo
Inglês
| MEDLINE | ID: mdl-34981329
11.
Neutralizing Type I Interferon Autoantibodies in Japanese Patients with Severe COVID-19.
J Clin Immunol
; 42(7): 1360-1370, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35764767
12.
Postchemotherapy immune status in infants with acute lymphoblastic leukemia: A report from the JPLSG MLL-10 trial.
Pediatr Blood Cancer
; 69(10): e29772, 2022 10.
Artigo
Inglês
| MEDLINE | ID: mdl-35796397
13.
Real-world results with IgPro20 for hypo- or agammaglobulinemia in Japan.
Pediatr Int
; 64(1): e15362, 2022 Jan.
Artigo
Inglês
| MEDLINE | ID: mdl-36151913
14.
Immunological abnormalities in patients with early-onset ataxia with ocular motor apraxia and hypoalbuminemia.
Clin Immunol
; 229: 108776, 2021 08.
Artigo
Inglês
| MEDLINE | ID: mdl-34118401
15.
Liver Abscess in Chronic Granulomatous Disease-Two Decades of Experience from a Tertiary Care Centre in North-West India.
J Clin Immunol
; 41(3): 552-564, 2021 04.
Artigo
Inglês
| MEDLINE | ID: mdl-33387158
16.
Hematopoietic Cell Transplantation for Severe Combined Immunodeficiency Patients: a Japanese Retrospective Study.
J Clin Immunol
; 41(8): 1865-1877, 2021 11.
Artigo
Inglês
| MEDLINE | ID: mdl-34448087
17.
Inherited CARD9 Deficiency in a Child with Invasive Disease Due to Exophiala dermatitidis and Two Older but Asymptomatic Siblings.
J Clin Immunol
; 41(5): 975-986, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33558980
18.
Clinical and Immunological Heterogeneity in Japanese Patients with Gain-of-Function Variants in STAT3.
J Clin Immunol
; 41(4): 780-790, 2021 05.
Artigo
Inglês
| MEDLINE | ID: mdl-33501615
19.
Hematopoietic Cell Transplantation with Reduced Intensity Conditioning Using Fludarabine/Busulfan or Fludarabine/Melphalan for Primary Immunodeficiency Diseases.
J Clin Immunol
; 41(5): 944-957, 2021 07.
Artigo
Inglês
| MEDLINE | ID: mdl-33527309
20.
Autosomal recessive complete STAT1 deficiency caused by compound heterozygous intronic mutations.
Int Immunol
; 32(10): 663-671, 2020 09 30.
Artigo
Inglês
| MEDLINE | ID: mdl-32603428