Affiliation:
1. Department of Pediatrics, Gifu Prefectural General Medical Center
Publisher
Japanese Society for Pediatric Nephrology
Subject
Literature and Literary Theory,History,Cultural Studies
Reference13 articles.
1. 1) Niaudet P, Rotig A: The kidney in mitochondrial cytopathies. Kidney Int 1997; 51: 1000–1007.
2. 3) Rötig A, Goutières F, Niaudet P, Rustin P, Chretien D, Guest G, Mikol J, Gubler MC, Munnich A: Deletion of mitochondrial DNA in patient with chronic tubulointerstitial nephritis. J Pediatr 1995; 126: 597–601.
3. 4) Jansen JJ, Maassen JA, van der Woude FJ, Lemmink HA, van den Ouweland JM, t’ Hart LM, Smeets HJ, Bruijn JA, Lemkes HH: Mutation in mitochondrial tRNA(Leu(UUR)) gene associated with progressive kidney disease. J Am Soc Nephrol 1997; 8: 1118–1124.
4. 8) Fujii H, Mori Y, Kayamori K, Igari T, Ito E, Akashi T, Noguchi Y, Kitamura K, Okado T, Terada Y, Kanda E, Rai T, Uchida S, Sasaki S: A familial case of mitochondrial disease resembling Alport syndrome. Clin Exp Nephrol 2008; 12: 159–163.
5. 10) Kuwertz-Bröking E, Koch HG, Marquardt T, Rossi R, Helmchen U, Müller-Höcker J, Harms E, Bulla M: Renal Fanconi syndrome: first sign of partial respiratory chain complex IV deficiency. Pediatr Nephrol 2000; 14: 495–498.