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Journal Abstract Search

218 related items for PubMed ID: 31165946

  • 1. Multiple urinary tract infections are associated with genotype and phenotype in adult polycystic kidney disease.
    Eroglu E, Kocyigit I, Cetin M, Zararsiz G, Imamoglu H, Bayramov R, Tastan S, Sipahioglu MH, Tokgoz B, Oymak O.
    Clin Exp Nephrol; 2019 Oct; 23(10):1188-1195. PubMed ID: 31165946
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  • 2. Pancreatic Cysts in Autosomal Dominant Polycystic Kidney Disease: Prevalence and Association with PKD2 Gene Mutations.
    Kim JA, Blumenfeld JD, Chhabra S, Dutruel SP, Thimmappa ND, Bobb WO, Donahue S, Rennert HE, Tan AY, Giambrone AE, Prince MR.
    Radiology; 2016 Sep; 280(3):762-70. PubMed ID: 27046073
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  • 3. Predicted Mutation Strength of Nontruncating PKD1 Mutations Aids Genotype-Phenotype Correlations in Autosomal Dominant Polycystic Kidney Disease.
    Heyer CM, Sundsbak JL, Abebe KZ, Chapman AB, Torres VE, Grantham JJ, Bae KT, Schrier RW, Perrone RD, Braun WE, Steinman TI, Mrug M, Yu AS, Brosnahan G, Hopp K, Irazabal MV, Bennett WM, Flessner MF, Moore CG, Landsittel D, Harris PC, HALT PKD and CRISP Investigators.
    J Am Soc Nephrol; 2016 Sep; 27(9):2872-84. PubMed ID: 26823553
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  • 4. Relationship of Seminal Megavesicles, Prostate Median Cysts, and Genotype in Autosomal Dominant Polycystic Kidney Disease.
    Zhang W, Stephens CJ, Blumenfeld JD, Behzadi AH, Donahue S, Bobb WO, Newhouse JH, Rennert H, Zhao Y, Prince MR.
    J Magn Reson Imaging; 2019 Mar; 49(3):894-903. PubMed ID: 30230107
    [Abstract] [Full Text] [Related]

  • 5. Effect of genotype on the severity and volume progression of polycystic liver disease in autosomal dominant polycystic kidney disease.
    Chebib FT, Jung Y, Heyer CM, Irazabal MV, Hogan MC, Harris PC, Torres VE, El-Zoghby ZM.
    Nephrol Dial Transplant; 2016 Jun; 31(6):952-60. PubMed ID: 26932689
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  • 6. Growth Pattern of Kidney Cyst Number and Volume in Autosomal Dominant Polycystic Kidney Disease.
    Bae KT, Zhou W, Shen C, Landsittel DP, Wu Z, Tao C, Chapman AB, Torres VE, Yu ASL, Mrug M, Bennett WM, Harris PC, Consortium for Radiologic Imaging Studies of Polycystic Kidney Disease (CRISP).
    Clin J Am Soc Nephrol; 2019 Jun 07; 14(6):823-833. PubMed ID: 31088850
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  • 7. The association of endothelin-1 levels with renal survival in polycystic kidney disease patients.
    Kocyigit I, Eroglu E, Kaynar AS, Kocer D, Kargi S, Zararsiz G, Bayramov R, Imamoglu H, Sipahioglu MH, Tokgoz B, Dundar M, Oymak O.
    J Nephrol; 2019 Feb 07; 32(1):83-91. PubMed ID: 30022320
    [Abstract] [Full Text] [Related]

  • 8. A comprehensive search for mutations in the PKD1 and PKD2 in Japanese subjects with autosomal dominant polycystic kidney disease.
    Kurashige M, Hanaoka K, Imamura M, Udagawa T, Kawaguchi Y, Hasegawa T, Hosoya T, Yokoo T, Maeda S.
    Clin Genet; 2015 Mar 07; 87(3):266-72. PubMed ID: 24611717
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  • 13. Combining genotype with height-adjusted kidney length predicts rapid progression of ADPKD.
    Chen EWC, Chong J, Valluru MK, Durkie M, Simms RJ, Harris PC, Ong ACM.
    Nephrol Dial Transplant; 2024 May 31; 39(6):956-966. PubMed ID: 38224954
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  • 14. Patients with Protein-Truncating PKD1 Mutations and Mild ADPKD.
    Lanktree MB, Guiard E, Akbari P, Pourafkari M, Iliuta IA, Ahmed S, Haghighi A, He N, Song X, Paterson AD, Khalili K, Pei YPC.
    Clin J Am Soc Nephrol; 2021 Mar 08; 16(3):374-383. PubMed ID: 33602752
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  • 16. Mutational Screening of PKD1 and PKD2 Genes in Iranian Population Diagnosed with Autosomal Dominant Polycystic Kidney Disease.
    Ranjzad F, Tara A, Basiri A, Aghdami N, Moghadasali R.
    Clin Lab; 2017 Jul 01; 63(7):1261-1267. PubMed ID: 28792715
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  • 17. Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing.
    Kim H, Park HC, Ryu H, Kim H, Lee HS, Heo J, Lee C, Kim NKD, Park WY, Hwang YH, Lee KB, Oh KH, Oh YK, Ahn C.
    Sci Rep; 2019 Nov 18; 9(1):16952. PubMed ID: 31740684
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  • 19. Mutational analysis in patients with Autosomal Dominant Polycystic Kidney Disease (ADPKD): Identification of five mutations in the PKD1 gene.
    Abdelwahed M, Hilbert P, Ahmed A, Mahfoudh H, Bouomrani S, Dey M, Hachicha J, Kamoun H, Keskes-Ammar L, Belguith N.
    Gene; 2018 Sep 10; 671():28-35. PubMed ID: 29860066
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