The 21 references in paper Elvira Andreeva F., Эльвира Андреева Фаатовна (2016) “Катамнез детей и подростков с поликистозом почек // The follow-up period of children and teenagers with polycystic kidney disease” / spz:neicon:nefr:y:2016:i:3:p:60-68

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Андреева ЭФ, Савенкова НД. Кистозные болезни почек у детей (обзор литературы). Нефрология 2012; (16)3: 34-47 [Andreeva EF, Savenkova ND. Cystic kidney disease in children (review). Nephrologija 2012; (16)3: 34-47]
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The classification of renal cystic diseases and other congenital malformations of the kidney and urinary tract. Arch Pathol Lab Med 2010; 134(4): 554-568
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Арутюнян СС, Савенкова НД. Характеристика почечных и внепочечных проявлений аутосомно-доминантного поликистоза почек у детей. Нефрология 2013; (17)3: 60–67 [Аrutyunyan SS, Savenkova ND. Characteristics of renal and extrarenal manifistations of autosomal dominant polycystic kidney disease in children. Nephrologija 2013; (17)3: 60-67]
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Арутюнян СС, Савенкова НД, Ларионова ВИ. Аутосомнодоминантный поликистоз почек у взрослых и детей (обзор литературы). Нефрология 2010; (14)3: 58-68 [Аrutyunyan SS, Savenkova ND, Larionova VI. Autosomal dominant polycystic kidney disease in children and adults. Nephrologija 2010; (14)3: 58-68]
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Huang JL, Woolf AS, Long DA. Angiogenesis and autosomal dominant polycystic kidney disease. Pediatr Nephrol 2013; 28: 1749-1755
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Grantham JJ. Rationale for early treatment of polycystic kidney disease. Pediatr Nephrol 2015; 30: 1053-1062
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Gansevoort RT, Arici M, Benzing T et al. Recommendations for the use of tolvaptan in autosomal dominant polycystic kidney disease: a position statement on behalf of the ERA-EDTA Working Groups on Inherited Kidney Disorders and European Renal Best Practice. Nephrol Dial Transplant 2016; 31: 337-348
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Spithoven EM, Kramer A, Meijer E et al. Renal replacement therapy for autosomal dominant polycystic kidney disease (ADPKD) in Europe: prevalence and survival-an analysis of data from the ERA-EDTA Registry. Nephrol Dial Transplant 2014; 29: 15-25
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Büscher R, Büscher AK, Weber S. Clinical manifestations of autosomal recessive polycystic kidney disease (ARPKD): kidneyrelated and non-kidney-related phenotypes. Pediatr Nephrol 2014; 29: 1915–1925
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Sweeney Jr WE, Avner ED. Diagnosis and management of childhood polycystic kidney disease. Pediatr Nephrol 2011; 26: 675-692
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Chapman AB, Devuyst O, Eckardt KU et al. Autosomaldominant polycystic kidney disease (ADPKD): executive summary from a Kidney Disease: Improving Global Outcomes (KDIGO) Controversies Conference. Kidney Int 2015; 88: 17-27
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Sweeney Jr WE, Avner ED. Pathophysiology of childhood polycystic kidney diseases: new insights into disease-specific therapy. Pediatric Research 2014; 75: 148–157
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Liebau MC, Serra AL. Looking at the (w)hole: magnet resonance imaging in polycystic kidney disease. Pediatr Nephrol 2013; 28:1771-1783. doi: 10.1007/s00467-012-2370-y
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Joshi SS, Paner GP, Chang SS. Polycystic Kidney Disease. In: The Kidney /edited by Hansel DE., Kane CJ., Paner GP., Chang SS. Springer. 2016; 19-35. doi: 10.1007/978-1-4939-3286-3
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Sweeney WE, Gunay-Aygun M, Patil A, Avner ED. Childhood Polycystic Kidney Disease. In: Pediatric Nephrology/ edited by Ellis Avner, William Harmon, Patrick Niaudet, Norishig Yoshikawa, Emma F., Goldstein S.L. – 7th ed. Springer. 2016; Part 6 (36): 11031153. 10.1007/978-3-662-43596-0_32
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21
Dell KM. The spectrum of polycystic kidney disease in children. Adv Chronic Kidney Dis 2011; 18 (5): 339-347. doi: 10.1053/j.ackd.2011.05.001 Сведения об авторе: Андреева Эльвира Фаатовна, к.м.н.
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