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A loss-of-function mutation in NaPi-IIa and renal Fanconi's syndrome.
Magen D, Berger L, Coady MJ, Ilivitzki A, Militianu D, Tieder M, Selig S, Lapointe JY, Zelikovic I, Skorecki K. Magen D, et al. Among authors: zelikovic i. N Engl J Med. 2010 Mar 25;362(12):1102-9. doi: 10.1056/NEJMoa0905647. N Engl J Med. 2010. PMID: 20335586 Free article.
Genetic disorders of renal phosphate transport.
Magen D, Zelikovic I, Skorecki K. Magen D, et al. Among authors: zelikovic i. N Engl J Med. 2010 Oct 28;363(18):1774; author reply 1774-5. doi: 10.1056/NEJMc1008407. N Engl J Med. 2010. PMID: 20979485 Free article. No abstract available.
Clinical quiz. Maternal chronic bilateral nephropathy.
Magen D, Blazer S, Zelikovic I. Magen D, et al. Among authors: zelikovic i. Pediatr Nephrol. 2002 Aug;17(8):695-8. doi: 10.1007/s00467-002-0856-8. Pediatr Nephrol. 2002. PMID: 12214597 No abstract available.
Fanconi-Bickel syndrome and autosomal recessive proximal tubulopathy with hypercalciuria (ARPTH) are allelic variants caused by GLUT2 mutations.
Mannstadt M, Magen D, Segawa H, Stanley T, Sharma A, Sasaki S, Bergwitz C, Mounien L, Boepple P, Thorens B, Zelikovic I, Jüppner H. Mannstadt M, et al. Among authors: zelikovic i. J Clin Endocrinol Metab. 2012 Oct;97(10):E1978-86. doi: 10.1210/jc.2012-1279. Epub 2012 Aug 3. J Clin Endocrinol Metab. 2012. PMID: 22865906 Free PMC article.
74 results