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Journal Abstract Search

291 related items for PubMed ID: 30225933

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  • 24. Potential effect of tolvaptan on polycystic liver disease for patients with ADPKD meeting the Japanese criteria of tolvaptan use.
    Mizuno H, Sekine A, Suwabe T, Ikuma D, Yamanouchi M, Hasegawa E, Sawa N, Ubara Y, Hoshino J.
    PLoS One; 2022; 17(2):e0264065. PubMed ID: 35176098
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  • 25. Carbohydrate antigen 19-9 is significantly elevated in autosomal dominant polycystic kidney disease.
    Fukasawa H, Kaneko M, Niwa H, Yasuda H, Kumagai H, Furuya R.
    Nephrology (Carlton); 2018 Mar; 23(3):210-216. PubMed ID: 28024168
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  • 26. Demographic and clinical characteristics of children with autosomal dominant polycystic kidney disease: a single center experience.
    Kasap Demir B, Mutlubaş F, Soyaltın E, Alparslan C, Arya M, Alaygut D, Arslansoyu Çamlar S, Berdeli A, Yavaşcan Ö.
    Turk J Med Sci; 2021 Apr 30; 51(2):772-777. PubMed ID: 33315352
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  • 27. Spleen phenotype in autosomal dominant polycystic kidney disease.
    Yin X, Prince WK, Blumenfeld JD, Zhang W, Donahue S, Bobb WO, Rennert H, Askin G, Barash I, Prince MR.
    Clin Radiol; 2019 Dec 30; 74(12):975.e17-975.e24. PubMed ID: 31563290
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  • 31. Polycystic liver disease genes: Practical considerations for genetic testing.
    Boerrigter MM, Bongers EMHF, Lugtenberg D, Nevens F, Drenth JPH.
    Eur J Med Genet; 2021 Mar 30; 64(3):104160. PubMed ID: 33556586
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  • 33. 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 30; 280(3):762-70. PubMed ID: 27046073
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  • 35. Young women with polycystic liver disease respond best to somatostatin analogues: a pooled analysis of individual patient data.
    Gevers TJ, Inthout J, Caroli A, Ruggenenti P, Hogan MC, Torres VE, Nevens F, Drenth JP.
    Gastroenterology; 2013 Aug 30; 145(2):357-65.e1-2. PubMed ID: 23665274
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  • 36. Liver cysts in Congolese patients with autosomal dominant polycystic kidney disease follow a family pattern.
    Assounga AG, Yacoubou Y, Makosso E, Ibara JR, Gombet T.
    S Afr Med J; 2003 Jul 30; 93(7):542-4. PubMed ID: 12939930
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  • 38. Volume Progression and Imaging Classification of Polycystic Liver in Early Autosomal Dominant Polycystic Kidney Disease.
    Bae KT, Tao C, Feldman R, Yu ASL, Torres VE, Perrone RD, Chapman AB, Brosnahan G, Steinman TI, Braun WE, Mrug M, Bennett WM, Harris PC, Srivastava A, Landsittel DP, Abebe KZ, CRISP and HALT PKD Consortium.
    Clin J Am Soc Nephrol; 2022 Mar 30; 17(3):374-384. PubMed ID: 35217526
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  • 40. Clinical manifestation, epidemiology, genetic basis, potential molecular targets, and current treatment of polycystic liver disease.
    Mahboobipour AA, Ala M, Safdari Lord J, Yaghoobi A.
    Orphanet J Rare Dis; 2024 Apr 26; 19(1):175. PubMed ID: 38671465
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