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Ocular involvement in a child with medullary nephrocalcinosis.
Kasap B, Alparslan C, Bal A, Konrad M, Yavaşcan Ö, Men G, Aksu N. Kasap B, et al. Pediatr Nephrol. 2013 Apr;28(4):627-30. doi: 10.1007/s00467-012-2237-2. Epub 2012 Jul 4. Pediatr Nephrol. 2013. PMID: 22760414 No abstract available.
Paracellin-1 gene mutation with multiple congenital abnormalities.
Türkmen M, Kasap B, Soylu A, Böber E, Konrad M, Kavukçu S. Türkmen M, et al. Among authors: kasap b. Pediatr Nephrol. 2006 Nov;21(11):1776-8. doi: 10.1007/s00467-006-0247-7. Epub 2006 Aug 22. Pediatr Nephrol. 2006. PMID: 16924549 Free article.
Juvenile linear scleroderma with unique forms of renal involvement.
Kasap B, Soylu A, Türkmen M, Göktay Y, Sarioğlu S, Oztürk C, Kasapçopur O, Kavukcu S. Kasap B, et al. Pediatr Nephrol. 2009 Oct;24(10):2041-5. doi: 10.1007/s00467-009-1206-x. Epub 2009 May 28. Pediatr Nephrol. 2009. PMID: 19475430
Megacalycosis: report of two cases.
Kasap B, Kavukçu S, Soylu A, Türkmen M, Seçil M. Kasap B, et al. Pediatr Nephrol. 2005 Jun;20(6):828-30. doi: 10.1007/s00467-004-1809-1. Epub 2005 Mar 23. Pediatr Nephrol. 2005. PMID: 15785940
114 results