Search Results - "Shiona, Shinichi"
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Impaired NEPHRIN localization in kidney organoids derived from nephrotic patient iPS cells
Published in Scientific reports (17-02-2021)“…Mutations in the NPHS1 gene, which encodes NEPHRIN, cause congenital nephrotic syndrome, resulting from impaired slit diaphragm (SD) formation in glomerular…”
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Clinical characteristics of HNF1B-related disorders in a Japanese population
Published in Clinical and experimental nephrology (01-09-2019)“…Background Hepatocyte nuclear factor 1β ( HNF1B ), located on chromosome 17q12, causes renal cysts and diabetes syndrome (RCAD). Moreover, various phenotypes…”
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溶連菌感染後に急性糸球体腎炎,紫斑病性腎炎を引き続き発症した 1 例
Published in 日本小児腎臓病学会雑誌 (2021)“…A 群β溶血性連鎖球菌(溶連菌)感染を契機として,溶連菌感染後急性糸球体腎炎(post-streptococcal acute glomerulonephritis: PSAGN),IgA 血管炎 (IgA vasculitis: IgAV),紫斑病性腎炎(Henoch-Schönlein purpura…”
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A case of IgA vasculitis, acute glomerulonephritis and Henoch-Schönlein purpura nephritis: successional complications of streptococcal infection
Published in Japanese journal of pediatric nephrology (2021)“…After infection with group A β-hemolytic streptococci, post-streptococcal acute glomerulonephritis (PSAGN), IgA vasculitis (IgAV), and Henoch-Schönlein purpura…”
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A case of IgA vasculitis, acute glomerulonephritis and Henoch-Schönlein purpura nephritis: successional complications of streptococcal infection
Published in Japanese journal of pediatric nephrology (2021)“…After infection with group A β-hemolytic streptococci, post-streptococcal acute glomerulonephritis (PSAGN), IgA vasculitis (IgAV), and Henoch-Schönlein purpura…”
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Protocol for the nationwide registry of patients with polycystic kidney disease: japanese national registry of PKD (JRP)
Published in Clinical and experimental nephrology (01-10-2024)“…Background Autosomal dominant polycystic kidney disease (ADPKD) and autosomal recessive polycystic kidney disease (ARPKD) are major genetic polycystic kidney…”
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