Found: 42
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Warfarin-induced toxic epidermal necrolysis in combination therapy of Henoch-Schönlein purpura nephritis: a case report.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Clinical characteristics and outcomes of immune-complex membranoproliferative glomerulonephritis and C3 glomerulopathy in Japanese children.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 9, p. 2679, doi. 10.1007/s00467-024-06377-7
- By:
- Publication type:
- Article
WT1 exon 10 missense variant in a pediatric patient with focal segmental glomerulosclerosis with embryonal hyperplasia.
- Published in:
- Pediatric Nephrology, 2024, v. 39, n. 7, p. 2083, doi. 10.1007/s00467-024-06293-w
- By:
- Publication type:
- Article
Anti-nephrin antibodies in steroid-sensitive nephrotic syndrome in Japanese children.
- Published in:
- 2024
- By:
- Publication type:
- Letter to the Editor
Use of renin-angiotensin system inhibitors as initial therapy in children with Henoch–Schönlein purpura nephritis of moderate severity.
- Published in:
- Pediatric Nephrology, 2022, v. 37, n. 8, p. 1845, doi. 10.1007/s00467-021-05395-z
- By:
- Publication type:
- Article
Comparison of clinical and genetic characteristics between Dent disease 1 and Dent disease 2.
- Published in:
- Pediatric Nephrology, 2020, v. 35, n. 12, p. 2319, doi. 10.1007/s00467-020-04701-5
- By:
- Publication type:
- Article
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-37985-w
- By:
- Publication type:
- Article
The utility of urinary CD80 as a diagnostic marker in patients with renal diseases.
- Published in:
- Scientific Reports, 2018, v. 8, n. 1, p. 1, doi. 10.1038/s41598-018-35798-2
- By:
- Publication type:
- Article
Study protocol: multicenter double-blind, randomized, placebo-controlled trial of rituximab for the treatment of childhood-onset early-stage uncomplicated frequently relapsing or steroid-dependent nephrotic syndrome (JSKDC10 trial).
- Published in:
- 2019
- By:
- Publication type:
- journal article
Case report: anti-glomerular basement membrane antibody disease with normal renal function.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Identification of novel OCRL isoforms associated with phenotypic differences between Dent disease-2 and Lowe syndrome.
- Published in:
- Nephrology Dialysis Transplantation, 2022, v. 37, n. 2, p. 262, doi. 10.1093/ndt/gfab274
- By:
- Publication type:
- Article
Steroid- and immunosuppressant-based protocol of Henoch-Schönlein purpura nephritis without angiotensin inhibitors in the acute phase.
- Published in:
- Minerva Pediatrics, 2023, v. 75, n. 2, p. 201, doi. 10.23736/S2724-5276.18.05324-0
- By:
- Publication type:
- Article
Impact of the State of Emergency during the COVID-19 Pandemic in 2020 on Asthma Exacerbations among Children in Kobe City, Japan.
- Published in:
- International Journal of Environmental Research & Public Health, 2021, v. 18, n. 21, p. 11407, doi. 10.3390/ijerph182111407
- By:
- Publication type:
- Article
Catheter‐related blood stream infection caused by Mycobacterium chelonae in a child with myeloid leukemia associated with Down syndrome.
- Published in:
- Clinical Case Reports, 2021, v. 9, n. 2, p. 835, doi. 10.1002/ccr3.3646
- By:
- Publication type:
- Article
Glomerular galactose-deficient IgA1 expression analysis in pediatric patients with glomerular diseases.
- Published in:
- Scientific Reports, 2020, v. 10, n. 1, p. N.PAG, doi. 10.1038/s41598-020-71101-y
- By:
- Publication type:
- Article
A Case of Juxtaglomerular Cell Tumor, or Reninoma, of the Kidney Treated by Retroperitoneoscopy-Assisted Nephron-Sparing Partial Nephrectomy Through a Small Pararectal Incision.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Effective response to azacitidine in a child with a second relapse of myeloid leukemia associated with Down syndrome after bone marrow transplantation.
- Published in:
- 2018
- By:
- Publication type:
- case study
Prevalence of Wilson disease based on genome databases in Japan.
- Published in:
- Pediatrics International, 2021, v. 63, n. 8, p. 918, doi. 10.1111/ped.14565
- By:
- Publication type:
- Article
Inherited salt‐losing tubulopathy: An old condition but a new category of tubulopathy.
- Published in:
- Pediatrics International, 2020, v. 62, n. 4, p. 428, doi. 10.1111/ped.14089
- By:
- Publication type:
- Article
Examination of the predicted prevalence of Gitelman syndrome by ethnicity based on genome databases.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-95521-6
- By:
- Publication type:
- Article
Development of an exon skipping therapy for X-linked Alport syndrome with truncating variants in COL4A5.
- Published in:
- Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-020-16605-x
- By:
- Publication type:
- Article
Maturity‐onset diabetes of the young type 5, presenting as diabetic ketoacidosis with alkalemia: A report of a case.
- Published in:
- Journal of Diabetes Investigation, 2022, v. 13, n. 5, p. 923, doi. 10.1111/jdi.13737
- By:
- Publication type:
- Article
Beneficial screening of Fabry disease in patients with hypohidrosis.
- Published in:
- Journal of Dermatology, 2022, v. 49, n. 2, p. 308, doi. 10.1111/1346-8138.16237
- By:
- Publication type:
- Article
Refractory Hypertension in Infantile-Onset Denys-Drash Syndrome.
- Published in:
- Tohoku Journal of Experimental Medicine, 2020, v. 252, n. 1, p. 45, doi. 10.1620/tjem.252.45
- By:
- Publication type:
- Article
All reported non-canonical splice site variants in GLA cause aberrant splicing.
- Published in:
- Clinical & Experimental Nephrology, 2023, v. 27, n. 9, p. 737, doi. 10.1007/s10157-023-02361-x
- By:
- Publication type:
- Article
Efficacy of combination therapy for childhood complicated focal IgA nephropathy.
- Published in:
- Clinical & Experimental Nephrology, 2022, v. 26, n. 6, p. 561, doi. 10.1007/s10157-022-02190-4
- By:
- Publication type:
- Article
Unilateral nephrectomy for young infants with congenital nephrotic syndrome of the Finnish type.
- Published in:
- Clinical & Experimental Nephrology, 2022, v. 26, n. 2, p. 162, doi. 10.1007/s10157-021-02141-5
- By:
- Publication type:
- Article
Clinical features of autosomal recessive polycystic kidney disease in the Japanese population and analysis of splicing in PKHD1 gene for determination of phenotypes.
- Published in:
- Clinical & Experimental Nephrology, 2022, v. 26, n. 2, p. 140, doi. 10.1007/s10157-021-02135-3
- By:
- Publication type:
- Article
X-chromosome inactivation patterns in females with Fabry disease examined by both ultra-deep RNA sequencing and methylation-dependent assay.
- Published in:
- Clinical & Experimental Nephrology, 2021, v. 25, n. 11, p. 1224, doi. 10.1007/s10157-021-02099-4
- By:
- Publication type:
- Article
Utility of glomerular Gd-IgA1 staining for indistinguishable cases of IgA nephropathy or Alport syndrome.
- Published in:
- Clinical & Experimental Nephrology, 2021, v. 25, n. 7, p. 779, doi. 10.1007/s10157-021-02054-3
- By:
- Publication type:
- Article
Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
Onset mechanism of a female patient with Dent disease 2.
- Published in:
- Clinical & Experimental Nephrology, 2020, v. 24, n. 10, p. 946, doi. 10.1007/s10157-020-01926-4
- By:
- Publication type:
- Article
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1.
- Published in:
- Clinical & Experimental Nephrology, 2020, v. 24, n. 7, p. 606, doi. 10.1007/s10157-020-01876-x
- By:
- Publication type:
- Article
Clinical characteristics of HNF1B-related disorders in a Japanese population.
- Published in:
- Clinical & Experimental Nephrology, 2019, v. 23, n. 9, p. 1119, doi. 10.1007/s10157-019-01747-0
- By:
- Publication type:
- Article
Pair analysis and custom array CGH can detect a small copy number variation in COQ6 gene.
- Published in:
- Clinical & Experimental Nephrology, 2019, v. 23, n. 5, p. 669, doi. 10.1007/s10157-018-1682-z
- By:
- Publication type:
- Article
Detection of copy number variations by pair analysis using next-generation sequencing data in inherited kidney diseases.
- Published in:
- Clinical & Experimental Nephrology, 2018, v. 22, n. 4, p. 881, doi. 10.1007/s10157-018-1534-x
- By:
- Publication type:
- Article
Effectiveness and nephrotoxicity of a 2-year medium dose of cyclosporine in pediatric patients with steroid-dependent nephrotic syndrome: determination of the need for follow-up kidney biopsy.
- Published in:
- Clinical & Experimental Nephrology, 2018, v. 22, n. 2, p. 413, doi. 10.1007/s10157-017-1444-3
- By:
- Publication type:
- Article
Detecting pathogenic deep intronic variants in Gitelman syndrome.
- Published in:
- American Journal of Medical Genetics. Part A, 2022, v. 188, n. 9, p. 2576, doi. 10.1002/ajmg.a.62885
- By:
- Publication type:
- Article
Heterozygous missense variant in TRPC6 in a boy with rapidly progressive infantile nephrotic syndrome associated with diffuse mesangial sclerosis.
- Published in:
- American Journal of Medical Genetics. Part A, 2021, v. 185, n. 7, p. 2175, doi. 10.1002/ajmg.a.62216
- By:
- Publication type:
- Article
Limited correlation between tumor markers and minimal residual disease detected by seven neuroblastoma-associated mRNAs in high-risk neuroblastoma patients.
- Published in:
- Molecular & Clinical Oncology, 2021, v. 15, n. 1, p. N.PAG, doi. 10.3892/mco.2021.2299
- By:
- Publication type:
- Article
Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay.
- Published in:
- Molecular Genetics & Genomic Medicine, 2020, v. 8, n. 8, p. 1, doi. 10.1002/mgg3.1342
- By:
- Publication type:
- Article
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome.
- Published in:
- Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 9, p. N.PAG, doi. 10.1002/mgg3.883
- By:
- Publication type:
- Article