Konjenital Böbrek Anomalileri
Öz
Anahtar Kelimeler
Kaynakça
- 1. Queisser-Luft A, Stolz G, Wiesel A, Schlaefer K, Spranger J. Malformations in newborn: results based on 30,940 infants and fetuses from the Mainz congenital birth defect monitoring system (1990-1998). Arch Gynecol Obstet 2002;266:163-7. http://dx.doi.org/10.1007/s00404-001-0265-4
- 2. Wiesel A, Queisser-Luft A, Clementi M, Bianca S, Stoll C, EUROSCAN Study Group. Prenatal detection of congenital renal malformations by fetal ultrasonographic examination: an analysis of 709.030 births in 12 European countries. Eur J Med Genet 2005;48:131-44. http://dx.doi.org/10.1016/j.ejmg.2005.02.003
- 3. Sanyanusin P, McNoe LA, Sullivan MJ, Weaver RG, Eccles MR. Mutation of PAX2 in two siblings with renalcoloboma syndrome. Hum Mol Genet 1995;4:2183-4. http://dx.doi.org/10.1093/hmg/4.11.2183
- 4. Edghill EL, Bingham C, Ellard S, Hattersley AT. Mutations in hepatocyte nuclear factor-1beta and their related phenotypes. J Med Genet 2006;43:84-90. http://dx.doi.org/10.1136/jmg.2005.032854
- 5. Song R, Yosypiv IV. Genetics of congenital anomalies of the kidney and urinary tract. Pediatr Nephrol 2011;26:353-64. http://dx.doi.org/10.1007/s00467-010-1629-4
- 6. Neild GH. Primary renal disease in young adults with renal failure. Nephrol Dial Transplant 2010;25:1025-32. http://dx.doi.org/10.1093/ndt/gfp653
- 7. Toka HR, Toka O, Hariri A, Nguyen HT. Congenital anomalies of kidney and urinary tract. Semin Nephrol 2010;30: 374-86. http://dx.doi.org/10.1016/j.semnephrol.2010.06.004
- 8. Seikaly MG, Ho PL, Emmett L, Fine RN, Tejani A. Chronic renal insufficiency in children: the 2001 Annual Report of the NAPRTCS. Pediatr Nephrol 2003;18:796-804. http://dx.doi.org/10.1007/s00467-003-1158-5
Ayrıntılar
Birincil Dil
Türkçe
Konular
-
Bölüm
-
Yazarlar
Zeynep Nagehan Yürük Yıldırım
Bu kişi benim
Yayımlanma Tarihi
1 Ekim 2013
Gönderilme Tarihi
-
Kabul Tarihi
-
Yayımlandığı Sayı
Yıl 2013 Cilt: 13 Sayı: 4