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Journal Abstract Search

277 related items for PubMed ID: 25088262

  • 21. A kidney-disease gene panel allows a comprehensive genetic diagnosis of cystic and glomerular inherited kidney diseases.
    Bullich G, Domingo-Gallego A, Vargas I, Ruiz P, Lorente-Grandoso L, Furlano M, Fraga G, Madrid Á, Ariceta G, Borregán M, Piñero-Fernández JA, Rodríguez-Peña L, Ballesta-Martínez MJ, Llano-Rivas I, Meñica MA, Ballarín J, Torrents D, Torra R, Ars E.
    Kidney Int; 2018 Aug; 94(2):363-371. PubMed ID: 29801666
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  • 23. Use of calcium excretion values to distinguish two forms of primary renal tubular hypokalemic alkalosis: Bartter and Gitelman syndromes.
    Bettinelli A, Bianchetti MG, Girardin E, Caringella A, Cecconi M, Appiani AC, Pavanello L, Gastaldi R, Isimbaldi C, Lama G.
    J Pediatr; 1992 Jan; 120(1):38-43. PubMed ID: 1731022
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  • 24. Recent advances in the molecular diagnosis of polycystic kidney disease.
    Bergmann C.
    Expert Rev Mol Diagn; 2017 Dec; 17(12):1037-1054. PubMed ID: 28952822
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  • 25. Polycystic kidney disease--the ciliary connection.
    Ong AC, Wheatley DN.
    Lancet; 2003 Mar 01; 361(9359):774-6. PubMed ID: 12620752
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  • 26. [Polycystic kidney diseases: molecular genetics and counselling].
    Lespinasse J, Fourcade J, Schir F.
    Nephrol Ther; 2006 Jul 01; 2(3):120-6. PubMed ID: 16890136
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  • 30. Early and Severe Polycystic Kidney Disease and Related Ciliopathies: An Emerging Field of Interest.
    Bergmann C.
    Nephron; 2019 Jul 01; 141(1):50-60. PubMed ID: 30359986
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  • 34. Rationale for early treatment of polycystic kidney disease.
    Grantham JJ.
    Pediatr Nephrol; 2015 Jul 01; 30(7):1053-62. PubMed ID: 25022529
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  • 36. Kidney stones and moderate proteinuria as the rare manifestations of Gitelman syndrome.
    Chen Q, Wang X, Min J, Wang L, Mou L.
    BMC Nephrol; 2021 Jan 07; 22(1):12. PubMed ID: 33413160
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  • 38. Diagnosis of monogenic chronic kidney diseases.
    Armstrong ME, Thomas CP.
    Curr Opin Nephrol Hypertens; 2019 Mar 07; 28(2):183-194. PubMed ID: 30601180
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  • 39. Renal, auricular, and ocular outcomes of Alport syndrome and their current management.
    Zhang Y, Ding J.
    Pediatr Nephrol; 2018 Aug 07; 33(8):1309-1316. PubMed ID: 28864840
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  • 40. Course of autosomal recessive polycystic kidney disease (ARPKD) in siblings: a clinical comparison of 20 sibships.
    Deget F, Rudnik-Schöneborn S, Zerres K.
    Clin Genet; 1995 May 07; 47(5):248-53. PubMed ID: 7554350
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