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Pediatric Nephrology
Literature
1.
Santo Y, Hirai H, Shima M, Yamagata M, Michigami T, Nakajima S, Ozono K (2004) Examination of megalin in renal tubular epithelium from patients with Dent disease. Pediatr Nephrol 19:612–615CrossRefPubMed
2.
Norden AGW, Lapsley M, Igarashi T, Kelleher CL, Lee PJ, Matsuyama T, Scheinman SJ, Shiraga H, Sundin DP, Thakker RV, Unwin RJ, Verroust P, Moestrup SK (2002) Urinary megalin deficiency implicates abnormal tubular endocytic function in Fanconi syndrome. J Am Soc Nephrol 13:125–133CrossRefPubMed
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Hoopes RR Jr, Raja KM, Koich A, Hueber P, Reid R, Knohl SJ, Scheinman SJ (2004) Evidence for genetic heterogeneity in Dent’s disease. Kidney Int 65:1615–1620CrossRefPubMed
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Thakker RV (2000) Pathogenesis of Dent’s disease and related syndromes of X-linked nephrolithiasis. Kidney Int 57:787–793CrossRefPubMed
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Marshansky V, Ausiello DA, Brown D (2002) Physiological importance of endosomal acidification: potential role in proximal tubulopathies. Curr Opin Nephrol Hypertens 11:527–537CrossRefPubMed
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Yamamoto K, Cox JPDT, Friedrich T, Christie PT, Bald M, Houtman PN, Lapsley MJ, Patzer L, Tsimaratos M, Hoff WGV, Yamaoka K, Jentsch TJ Thakker RV (2000) Characterization of renal chloride channel (CLCN5) mutations in Dent’s disease. J Am Soc Nephrol 11:1460–1468PubMed
Metadata
Title
Megalin and proximal renal tubular dysfunction in Dent disease
Author
Toru Watanabe
Publication date
01-11-2004
Publisher
Springer-Verlag
Published in
Pediatric Nephrology / Issue 11/2004
Print ISSN: 0931-041X
Electronic ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-004-1605-y

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