Detalhe da pesquisa
1.
Outcome of immunosuppression in children with IgA vasculitis-related nephritis.
Nephrol Dial Transplant
; 2024 Jan 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-38211969
2.
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children.
Pediatr Nephrol
; 2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38662234
3.
Trimerization profile of type IV collagen COL4A5 exon deletion in X-linked Alport syndrome.
Clin Exp Nephrol
; 2024 Apr 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-38658441
4.
Rituximab in combination with cyclosporine and steroid pulse therapy for childhood-onset multidrug-resistant nephrotic syndrome: a multicenter single-arm clinical trial (JSKDC11 trial).
Clin Exp Nephrol
; 28(4): 337-348, 2024 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-38010466
5.
A multicenter retrospective study of calcineurin inhibitors in nephrotic syndrome secondary to podocyte gene variants.
Kidney Int
; 103(5): 962-972, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-36898413
6.
Clinical and pathological investigation of oligomeganephronia.
Pediatr Nephrol
; 38(3): 757-762, 2023 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-35861872
7.
Is influenza vaccination associated with nephrotic syndrome relapse in children? A multicenter prospective study.
Pediatr Nephrol
; 38(7): 2107-2116, 2023 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-36449102
8.
Long-term outcome of combination therapy with corticosteroids, mizoribine and RAS inhibitors as initial therapy for severe childhood IgA vasculitis with nephritis.
Pediatr Nephrol
; 38(12): 4023-4031, 2023 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37380934
9.
Aberrant splicing caused by exonic single nucleotide variants positioned 2nd or 3rd to the last nucleotide in the COL4A5 gene.
Clin Exp Nephrol
; 27(3): 218-226, 2023 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-36371577
10.
All reported non-canonical splice site variants in GLA cause aberrant splicing.
Clin Exp Nephrol
; 27(9): 737-746, 2023 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-37254000
11.
Comprehensive genetic analysis using next-generation sequencing for the diagnosis of nephronophthisis-related ciliopathies in the Japanese population.
J Hum Genet
; 67(7): 427-440, 2022 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-35140360
12.
BCS1L mutations produce Fanconi syndrome with developmental disability.
J Hum Genet
; 67(3): 143-148, 2022 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-34650211
13.
Detecting pathogenic deep intronic variants in Gitelman syndrome.
Am J Med Genet A
; 188(9): 2576-2583, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35785516
14.
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome.
Nephrol Dial Transplant
; 37(2): 262-270, 2022 01 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-34586410
15.
An updated view of the pathogenesis of steroid-sensitive nephrotic syndrome.
Pediatr Nephrol
; 37(9): 1957-1965, 2022 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-35006356
16.
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch-Schönlein purpura nephritis of moderate severity.
Pediatr Nephrol
; 37(8): 1845-1853, 2022 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-35015121
17.
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
Clin Exp Nephrol
; 26(2): 140-153, 2022 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-34536170
18.
Efficacy of combination therapy for childhood complicated focal IgA nephropathy.
Clin Exp Nephrol
; 26(6): 561-570, 2022 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-35138499
19.
X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay.
Clin Exp Nephrol
; 25(11): 1224-1230, 2021 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-34128148
20.
Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome.
Clin Exp Nephrol
; 25(7): 779-787, 2021 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-33743099