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Journal Abstract Search

243 related items for PubMed ID: 35549682

  • 1.
    ; . PubMed ID:
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  • 3. Clinical features and genetic analysis of 15 Chinese children with dent disease.
    Li Q, Yang Z, Zang R, Liu S, Yu L, Wang J, Wang C, Wang X, Sun S.
    Ren Fail; 2024 Dec; 46(1):2349133. PubMed ID: 38726999
    [Abstract] [Full Text] [Related]

  • 4. A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency.
    Bogdanović R, Draaken M, Toromanović A, Dordević M, Stajić N, Ludwig M.
    Pediatr Nephrol; 2010 Nov; 25(11):2363-8. PubMed ID: 20680351
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    Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, Lieske JC, Milliner DS, Beara-Lasic L, Harris P, Cogal A, Abrash E.
    ; 1993 Nov. PubMed ID: 22876375
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  • 7. Observations of a large Dent disease cohort.
    Blanchard A, Curis E, Guyon-Roger T, Kahila D, Treard C, Baudouin V, Bérard E, Champion G, Cochat P, Dubourg J, de la Faille R, Devuyst O, Deschenes G, Fischbach M, Harambat J, Houillier P, Karras A, Knebelmann B, Lavocat MP, Loirat C, Merieau E, Niaudet P, Nobili F, Novo R, Salomon R, Ulinski T, Jeunemaître X, Vargas-Poussou R.
    Kidney Int; 2016 Aug; 90(2):430-439. PubMed ID: 27342959
    [Abstract] [Full Text] [Related]

  • 8. A patient with Dent disease and features of Bartter syndrome caused by a novel mutation of CLCN5.
    Okamoto T, Tajima T, Hirayama T, Sasaki S.
    Eur J Pediatr; 2012 Feb; 171(2):401-4. PubMed ID: 21932010
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  • 9. [Clinical features and genetic variants of Dent disease in 10 children].
    Zhao SL, Zhao F, Sha YG, Chen QX, Cheng XQ, Huang SM.
    Zhonghua Er Ke Za Zhi; 2018 Apr 02; 56(4):289-293. PubMed ID: 29614570
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  • 11. Multicenter study of the clinical features and mutation gene spectrum of Chinese children with Dent disease.
    Ye Q, Shen Q, Rao J, Zhang A, Zheng B, Liu X, Shen Y, Chen Z, Wu Y, Hou L, Jian S, Wei M, Ma M, Sun S, Li Q, Dang X, Wang Y, Xu H, Mao J, for Chinese Children Genetic Kidney Disease Database (CCGKDD), “Internet Plus” Nephrology Alliance of National Center for Children's Care.
    Clin Genet; 2020 Mar 02; 97(3):407-417. PubMed ID: 31674016
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  • 12. [Two cases of Dent disease type 1 with Bartter-like phenotype and literature review].
    Cheng M, Meng X, Liu M, Gong CX.
    Zhonghua Yi Xue Za Zhi; 2024 Sep 03; 104(34):3256-3259. PubMed ID: 39193613
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  • 14. Japanese Dent disease has a wider clinical spectrum than Dent disease in Europe/USA: genetic and clinical studies of 86 unrelated patients with low-molecular-weight proteinuria.
    Sekine T, Komoda F, Miura K, Takita J, Shimadzu M, Matsuyama T, Ashida A, Igarashi T.
    Nephrol Dial Transplant; 2014 Feb 03; 29(2):376-84. PubMed ID: 24081861
    [Abstract] [Full Text] [Related]

  • 15. Phenotypic spectrum and antialbuminuric response to angiotensin converting enzyme inhibitor and angiotensin receptor blocker therapy in pediatric Dent disease.
    Deng H, Zhang Y, Xiao H, Yao Y, Zhang H, Liu X, Su B, Guan N, Zhong X, Wang S, Ding J, Wang F.
    Mol Genet Genomic Med; 2020 Aug 03; 8(8):e1306. PubMed ID: 32495484
    [Abstract] [Full Text] [Related]

  • 16. [Clinical and genetic analysis of Dent' s disease in 6 Chinese children with low molecular weight proteinuria].
    Zhu BZ, Li P, Huang JP.
    Zhonghua Er Ke Za Zhi; 2010 May 03; 48(5):329-33. PubMed ID: 20654030
    [Abstract] [Full Text] [Related]

  • 17. Expanding the phenotype of proteinuria in Dent disease. A case series.
    Cramer MT, Charlton JR, Fogo AB, Fathallah-Shaykh SA, Askenazi DJ, Guay-Woodford LM.
    Pediatr Nephrol; 2014 Oct 03; 29(10):2051-4. PubMed ID: 24810952
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  • 19. Nephrolithiasis, kidney failure and bone disorders in Dent disease patients with and without CLCN5 mutations.
    Anglani F, D'Angelo A, Bertizzolo LM, Tosetto E, Ceol M, Cremasco D, Bonfante L, Addis MA, Del Prete D, Dent Disease Italian Network.
    Springerplus; 2015 Oct 03; 4():492. PubMed ID: 26389017
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