Results 51 to 60 of about 20,236 (164)
A Rare and Serious Complication of Percutaneous Renal Biopsy: Retroperitoneal Hemorrhage
İstanbul Medical Journal, 2019 Renal biopsy is the gold standard diagnostic method in adults with the renal parenchymal disease. Retroperitoneal hemorrhage is one of the rare and most severe complications of percutaneous renal biopsy.
Tamer Selen +3 more
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Kidney International, 1997 Familial idiopathic low-molecular-weight proteinuria (FILMWP) is a renal proximal tubulopathy that occurs predominantly in males. FILMWP is characterized by mild proteinuria consisting of low-molecular-weight proteinuria, aminoaciduria and relatively conserved renal function, but without rickets. To determine whether FILMWP is related to the CLCN5 gene,
Nakazato, Hitoshi +8 more
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Tubular markers in children with insulin-dependent diabetes mellitus
The Turkish Journal of Pediatrics, 1997 The aim of the present study was to investigate the prevalence of tubular dysfunction and to assess the clinical significance of low-molecular-weight proteinuria and enzymuria in children with insulin-dependent diabetes mellitus (IDDM).
S Calişkan +7 more
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Nephrotoxicity-induced proteinuria increases biomarker diagnostic thresholds in acute kidney injury
BMC Nephrology, 2017 Background Paraquat ingestion is frequently fatal. While biomarkers of kidney damage increase during paraquat-induced acute kidney injury (AKI), significant concurrent proteinuria may alter diagnostic thresholds for diagnosis and prognosis to an unknown ...
Fahim Mohamed +8 more
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Analysis in the CLCN5 gene in patients with familial idiopathic low-molecular-weight proteinuria.
Nihon Shoni Jinzobyo Gakkai Zasshi, 1998 家族性特発性低分子蛋白尿症 (familial idiopathic low-molecular-weight proteinuria: FILMWP) は，低分子蛋白尿を呈する腎尿細管障害で本邦にて報告された。一方，腎結石症を伴うDent病などの3つの遺伝性腎尿細管障害が欧米で報告され，クロライドチャンネルCLCN5遺伝子の異常であることが報告された。これらの疾患には臨床上の類似性がみられるが，FILMWPでは腎不全やくる病がないことで区別される。 私達はFILMWP患者5例についてCLCN5遺伝子を解析し，一塩基挿入2例，一塩基欠失2例，ナンセンス変異1例を認めた。FILMWPの多くは本遺伝子の異常でおこると考えられ，これら4つの腎尿細管疾患は1つの疾患の亜型と考えられる ...
Hitoshi Nakazato +10 more
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Case Report: Early acute kidney failure in an 11-year-old boy with Dent disease type 1
Frontiers in PediatricsDent disease type 1 (Dent 1) is a rare X-linked genetic condition which impacts kidney function and is caused by pathogenic variants in CLCN5.
Nicolette Murphey +4 more
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Zdravniški Vestnik, 2017 Dent disease is an x-linked disorder of proximal renal tubular dysfunction that occurs almost exclusively in males. It is characterized by significant, mostly low molecular weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and ...
Rina R Rus, Kristina Vogrin
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Journal of International Medical ResearchDent disease is a rare disease with proximal renal tubular dysfunction, and is characterized by low-molecular-weight proteinuria, hypercalciuria, nephrocalcinosis, nephrolithiasis, and chronic kidney disease. Renal failure slowly progresses and end-stage
Youying Mao +4 more
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Kidney MedicineLight-chain proximal tubulopathy (LCPT) is typically characterized by the intracytoplasmic deposition of light chains within the proximal tubular epithelial cells, which is usually classified into crystalline and noncrystalline subgroups.
Huizi Zhang, Chunyun Zhang, Hua Su
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BiomoleculesThe metabolic response to a maximal exercise test in physically inactive adults remains poorly understood, particularly regarding the role of adiponectin, an adipokine with insulin-sensitizing and anti-inflammatory properties.
Johnattan Cano-Montoya +7 more
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