References
- 1. Renkema KY, Winyard PJ, Skovorodkin IN et al. Novel perspectives for investigating congenital anomalies of the kidney and urinary tract (CAKUT). Nephrol Dial Transplant. 2011. 26; 3843-3851.10.1093/ndt/gfr65522121240
- 2. Palacios Loro ML, Segura Ramírez DK, Ordoñez Álvarez FA, Santos Rodríguez F. Congenital anomalies of the kidney and urinary tract. A vision for the paediatrician. An Pediatr (Barc). 2015; 83(6):442.
- 3. Weber S. Novel genetic aspects of congenital anomalies of kidney and urinary tract. Curr Opin Pediatr. 2012; 24(2):212-8.10.1097/MOP.0b013e32834fdbd422245908
- 4. Sanna-Cherchi S, Caridi G, Weng PL et al. Localization of a gene for nonsyndromic renal hypodysplasia to chromosome 1p32-33. Am J Hum Genet. 2007; 80: 539-549.10.1086/512248182109917273976
- 5. Sanna-Cherchi S, Sampogna RV, Papeta N et al. Mutations in DSTYK and dominant urinary tract malformations. New Eng J Med. 2013; 369: 621-629.10.1056/NEJMoa1214479384639123862974
- 6. Vivante A, Kohl S, Hwang DY et al. Single-gene causes of congenital anomalies of the kidney and urinary tract (CAKUT) in humans. Pediatr Nephrol. 2014; 29(4):695-704.10.1007/s00467-013-2684-4467640524398540
- 7. Song R, Yosypiv IV. Genetics of congenital anomalies of the kidney and urinary tract. Pediatr Nephrol. 2011; 26(3):353-364.10.1007/s00467-010-1629-420798957
- 8. Tulassay T, Vásárhelyi B. Birth weight and renal function. Curr Opin Nephrol Hypertens. 2002; 11(3):347-352.10.1097/00041552-200205000-0001311981267
- 9. Lee PA, Chernausek SD, Hokken-Koelega AC, Czernichow P; International Small for Gestational Age Advisory Board. International Small for Gestational Age Advisory Board consensus development conference statement: management of short children born small for gestational age, April 24-October 1, 2001. Pediatrics. 2003; 111(6 Pt 1):1253-1261.10.1542/peds.111.6.125312777538
- 10. Zhang B, Wang H, Sun N et al. Incidence, diagnosis and treatment of children’s congenital abnormalities of the kidney and urinary tract detected in ultrasound screening. Zhonghua Er Ke Za Zhi. 2011; 49(7):534-538.
- 11. Brenner BM, Anderson S. The interrelationships among filtration surface area, blood pressure, and chronic renal disease. J Cardiovasc Pharmacol. 1992; 19 (6): S1-S7.10.1097/00005344-199219006-000021382155
- 12. Keijzer-Veen MG, Schrevel M, Finken MJ et al. Dutch POPS-19 Collaborative Study Group. Microalbuminuria and lower glomerular filtration rate at young adult age in subjects born very premature and after intrauterine growth retardation. J Am Soc Nephrol. 2005; 16(9):2762-2768.10.1681/ASN.200409078315987756
- 13. Karlberg J, Schaefer F, Hennicke M et al. Early age-dependent growth impairment in chronic renal failure. European Study Group for Nutritional Treatment of Chronic Renal Failure in Childhood. Pediatr Nephrol. 1996; 10(3):283-287.10.1007/BF008667618792391
- 14. Franke D, Völker S, Haase S et al. Prematurity, small for gestational age and perinatal parameters in children with congenital, hereditary and acquired chronic kidney disease. Nephrol Dial Transplant. 2010; 25(12):3918-24.10.1093/ndt/gfq30020513774
- 15. Zivicnjak M, Franke D, Filler G et al. Growth impairment shows an age-dependent pattern in boys with chronic kidney disease. Pediatr Nephrol. 2007; 22(3):420-429.10.1007/s00467-006-0345-617131161
- 16. Mehls O, Lindberg A, Nissel R et al. Predicting the response to growth hormone treatment in short children with chronic kidney disease. J Clin Endocrinol Metab. 2010; 95(2):686-692.10.1210/jc.2009-111420008024
- 17. Toka HR, Toka O, Hariri A, Nguyen HT. Congenital anomalies of kidney and urinary tract. Semin Nephrol. 2010; 30(4):374-386.10.1016/j.semnephrol.2010.06.00420807610
- 18. Sanna-Cherchi S, Ravani P, Corbani V et al. Renal outcome in patients with congenital anomalies of the kidney and urinary tract. Kidney Int. 2009; 76(5):528-533.10.1038/ki.2009.22019536081
- 19. Weber S, Moriniere V, Knuppel T et al. Prevalence of mutations in renal developmental genes in children with renal hypodysplasia: results of the ESCAPE study. J Am Soc Nephrol. 2006; 17:2864-2870.10.1681/ASN.200603027716971658
- 20. Thomas R, Sanna-Cherchi S, Warady BA et al. HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort. Pediatr Nephrol. 2011; 26: 897-903.10.1007/s00467-011-1826-9325747021380624
- 21. Argente J, Mehls O, Barrios V. Growth and body composition in very young SGA children. Pediatr Nephrol. 2010; 25(4):679-685.10.1007/s00467-009-1432-220108001