Anomalije bubrega (Serbian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Anomalije bubrega" in Serbian language version.

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8nih.gov

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6doi.org

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1nature.com

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1web.archive.org

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1stetoskop.info

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1nejm.org

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doi.org

Hofmann, A. D.; Duess, J. W.; Puri, P. (август 2014). „Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: A systematic review”. Pediatr Surg Int. 30 (8): 757—61. PMID 24974188. doi:10.1007/s00383-014-3529-3. .
Song, R.; Yosypiv, I. V. (март 2011). „Genetics of congenital anomalies of the kidney and urinary tract”. Pediatric Nephrology. 26 (3): 353—64. PMID 20798957. doi:10.1007/s00467-010-1629-4. .
Grantham, Jared (2. 10. 2008). „Autosomal Dominant Polycystic Kidney Disease”. New England Journal of Medicine. 359 (14): 1477—1485. PMID 18832246. doi:10.1056/NEJMcp0804458.
Lee, K.; Battini, L.; Gusella, G. L. (2011). „Cilium, centrosome and cell cycle regulation in polycystic kidney disease”. Biochimica et Biophysica Acta. 1812 (10): 1263—71. PMC 3138898 . PMID 21376807. doi:10.1016/j.bbadis.2011.02.008.
Pirson, Y. (2010). „Extrarenal manifestations of autosomal dominant polycystic kidney disease”. Advances in Chronic Kidney Disease. 17 (2): 173—80. PMID 20219620. doi:10.1053/j.ackd.2010.01.003. .
Wen, J. (2011). „Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease”. Clinical and Translational Science. 4 (6): 460—5. PMC 3252199 . PMID 22212229. doi:10.1111/j.1752-8062.2011.00306.x. .

nature.com

Torres, Vicente (20. 5. 2009). „Autosomal dominant polycystic kidney disease: the last 3 years”. Kidney International. 76 (2): 149—168.

nejm.org

Grantham, Jared (2. 10. 2008). „Autosomal Dominant Polycystic Kidney Disease”. New England Journal of Medicine. 359 (14): 1477—1485. PMID 18832246. doi:10.1056/NEJMcp0804458.

nih.gov

ncbi.nlm.nih.gov

Zhang, B.; Wang, H.; Sun, N.; Jia, L. Q.; Shen, Y. (јул 2011). „Incidence, diagnosis and treatment of children's congenital abnormalities of the kidney and urinary tract detected in ultrasound screening”. Zhonghua Er Ke Za Zhi. 49 (7): 534—8. PMID 22088185. .
Hofmann, A. D.; Duess, J. W.; Puri, P. (август 2014). „Congenital anomalies of the kidney and urinary tract (CAKUT) associated with Hirschsprung's disease: A systematic review”. Pediatr Surg Int. 30 (8): 757—61. PMID 24974188. doi:10.1007/s00383-014-3529-3. .
Song, R.; Yosypiv, I. V. (март 2011). „Genetics of congenital anomalies of the kidney and urinary tract”. Pediatric Nephrology. 26 (3): 353—64. PMID 20798957. doi:10.1007/s00467-010-1629-4. .
DALGAARD, O. Z. (1957). „Bilateral polycystic disease of the kidneys; a follow-up of two hundred and eighty-four patients and their families”. Acta Med. Scand. Suppl. 328: 1—255. PMID 13469269.
Grantham, Jared (2. 10. 2008). „Autosomal Dominant Polycystic Kidney Disease”. New England Journal of Medicine. 359 (14): 1477—1485. PMID 18832246. doi:10.1056/NEJMcp0804458.
Lee, K.; Battini, L.; Gusella, G. L. (2011). „Cilium, centrosome and cell cycle regulation in polycystic kidney disease”. Biochimica et Biophysica Acta. 1812 (10): 1263—71. PMC 3138898 . PMID 21376807. doi:10.1016/j.bbadis.2011.02.008.
Pirson, Y. (2010). „Extrarenal manifestations of autosomal dominant polycystic kidney disease”. Advances in Chronic Kidney Disease. 17 (2): 173—80. PMID 20219620. doi:10.1053/j.ackd.2010.01.003. .
Wen, J. (2011). „Congenital hepatic fibrosis in autosomal recessive polycystic kidney disease”. Clinical and Translational Science. 4 (6): 460—5. PMC 3252199 . PMID 22212229. doi:10.1111/j.1752-8062.2011.00306.x. .

stetoskop.info

„Policistični bubrezi”. Стетоскоп. 12. 6. 2007. Архивирано из оригинала 16. 09. 2011. г. Приступљено 16. 8. 2011.

web.archive.org

„Policistični bubrezi”. Стетоскоп. 12. 6. 2007. Архивирано из оригинала 16. 09. 2011. г. Приступљено 16. 8. 2011.