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1.
Changes in bone turnover markers after discontinuing long-term glucocorticoid administration in children with idiopathic nephrotic syndrome: a multicenter retrospective observational study.
Pediatr Nephrol
; 38(10): 3285-3296, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37052692
2.
The effect of rituximab on the quality of life of children with refractory nephrotic syndrome.
Pediatr Int
; 64(1): e14725, 2022 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-33826766
3.
Absent X-linked inhibitor of apoptosis protein expression in T cell blasts and causal mutations including non-coding deletion.
Pediatr Int
; 64(1): e14892, 2022 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-34145698
4.
Heterozygous Mutations in OAS1 Cause Infantile-Onset Pulmonary Alveolar Proteinosis with Hypogammaglobulinemia.
Am J Hum Genet
; 102(3): 480-486, 2018 03 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29455859
5.
Efficacy of primary treatment with immunoglobulin plus ciclosporin for prevention of coronary artery abnormalities in patients with Kawasaki disease predicted to be at increased risk of non-response to intravenous immunoglobulin (KAICA): a randomised controlled, open-label, blinded-endpoints, phase 3 trial.
Lancet
; 393(10176): 1128-1137, 2019 Mar 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-30853151
6.
Glucose metabolism disorders in children with refractory nephrotic syndrome.
Pediatr Nephrol
; 35(4): 649-657, 2020 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-31950245
7.
A deep intronic mutation of c.1166-285â¯Tâ¯>â¯G in SLC46A1 is shared by four unrelated Japanese patients with hereditary folate malabsorption (HFM).
Clin Immunol
; 208: 108256, 2019 11.
Artículo
en Inglés
| MEDLINE | ID: mdl-31494288
8.
Persistent systemic rotavirus vaccine infection in a child with X-linked severe combined immunodeficiency.
J Med Virol
; 91(6): 1008-1013, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30687932
9.
Periodically repeated rituximab administrations in children with refractory nephrotic syndrome: 2-year multicenter observational study.
Pediatr Nephrol
; 34(1): 87-96, 2019 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30141179
10.
Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.
Clin Exp Nephrol
; 23(5): 669-675, 2019 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-30584653
11.
Mesangial C4d deposition at diagnosis in childhood immunoglobulin A nephropathy.
Pediatr Int
; 61(11): 1133-1139, 2019 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-31237969
12.
Evaluation of systemic activity of pediatric primary Sjögren's syndrome by EULAR Sjögren's syndrome disease activity index (ESSDAI).
Mod Rheumatol
; 29(1): 130-133, 2019 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-29529894
13.
Myositis-specific autoantibodies in Japanese patients with juvenile idiopathic inflammatory myopathies.
Mod Rheumatol
; 29(2): 351-356, 2019 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-29532710
14.
Genetic basis for childhood interstitial lung disease among Japanese infants and children.
Pediatr Res
; 83(2): 477-483, 2018 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-29569581
15.
Evaluation of a Novel Immunochromatographic Assay for Detection of Human Adenoviruses from Throat Swab Samples Compared with Real-time PCR.
Clin Lab
; 64(10): 1777-1781, 2018 Oct 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30336514
16.
Clinical effectiveness of four neuraminidase inhibitors (oseltamivir, zanamivir, laninamivir, and peramivir) for children with influenza A and B in the 2014-2015 to 2016-2017 influenza seasons in Japan.
J Infect Chemother
; 24(6): 449-457, 2018 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-29487035
17.
Progression of palindromic rheumatism to juvenile idiopathic arthritis in a Japanese girl carrying heterozygous L110P-E148Q substitutions of MEFV gene.
Mod Rheumatol
; 28(2): 365-368, 2018 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-26457478
18.
Difficulty in the diagnosis of bone and joint pain associated with pediatric acute leukemia; comparison with juvenile idiopathic arthritis.
Mod Rheumatol
; 28(1): 108-113, 2018 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-28612674
19.
A heterozygous dominant-negative mutation in the coiled-coil domain of STAT1 is the cause of autosomal-dominant Mendelian susceptibility to mycobacterial diseases.
Clin Immunol
; 174: 24-31, 2017 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-27856304
20.
A novel heterozygous mutation of the WFS1 gene leading to constitutive endoplasmic reticulum stress is the cause of Wolfram syndrome.
Pediatr Diabetes
; 18(8): 934-941, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-28271591