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Journal Abstract Search

152 related items for PubMed ID: 23110775

  • 21. Unusual adult-onset manifestation of an attenuated Bartter's syndrome type IV renal phenotype caused by a mutation in BSND.
    Brum S, Rueff J, Santos JR, Calado J.
    Nephrol Dial Transplant; 2007 Jan; 22(1):288-9. PubMed ID: 16935888
    [No Abstract] [Full Text] [Related]

  • 22. Deletion of exons 2-4 in the BSND gene causes severe antenatal Bartter syndrome.
    Bircan Z, Harputluoglu F, Jeck N.
    Pediatr Nephrol; 2009 Apr; 24(4):841-4. PubMed ID: 18843510
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  • 23. ClC-K chloride channels: emerging pathophysiology of Bartter syndrome type 3.
    Andrini O, Keck M, Briones R, Lourdel S, Vargas-Poussou R, Teulon J.
    Am J Physiol Renal Physiol; 2015 Jun 15; 308(12):F1324-34. PubMed ID: 25810436
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  • 25. Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
    Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R.
    Nephrol Dial Transplant; 2009 May 15; 24(5):1455-64. PubMed ID: 19096086
    [Abstract] [Full Text] [Related]

  • 26. Reduced Membrane Insertion of CLC-K by V33L Barttin Results in Loss of Hearing, but Leaves Kidney Function Intact.
    Tan H, Bungert-Plümke S, Fahlke C, Stölting G.
    Front Physiol; 2017 May 15; 8():269. PubMed ID: 28555110
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  • 28. Activation of renal ClC-K chloride channels depends on an intact N terminus of their accessory subunit barttin.
    Wojciechowski D, Thiemann S, Schaal C, Rahtz A, de la Roche J, Begemann B, Becher T, Fischer M.
    J Biol Chem; 2018 Jun 01; 293(22):8626-8637. PubMed ID: 29674316
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  • 29. Identification and functional analysis of novel mutations of the CLCNKB gene in Chinese patients with classic Bartter syndrome.
    Yu Y, Xu C, Pan X, Ren H, Wang W, Meng X, Huang F, Chen N.
    Clin Genet; 2010 Feb 01; 77(2):155-62. PubMed ID: 19807735
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  • 30. [Bartter's syndrome].
    Daniluk U, Kaczmarski M, Wasilewska J, Matuszewska E, Semeniuk J, Sidor K, Krasnow A.
    Pol Merkur Lekarski; 2004 May 01; 16(95):484-9. PubMed ID: 15518434
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  • 31. Functional severity of CLCNKB mutations correlates with phenotypes in patients with classic Bartter's syndrome.
    Cheng CJ, Lo YF, Chen JC, Huang CL, Lin SH.
    J Physiol; 2017 Aug 15; 595(16):5573-5586. PubMed ID: 28555925
    [Abstract] [Full Text] [Related]

  • 32. Hypokalemic paralysis in a middle-aged female with classic Bartter syndrome.
    Chiang WF, Lin SH, Chan JS, Lin SH.
    Clin Nephrol; 2014 Feb 15; 81(2):146-50. PubMed ID: 22854165
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  • 35. Bartter syndrome.
    Hebert SC.
    Curr Opin Nephrol Hypertens; 2003 Sep 15; 12(5):527-32. PubMed ID: 12920401
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  • 36. Genetic basis of Bartter syndrome in Korea.
    Lee BH, Cho HY, Lee H, Han KH, Kang HG, Ha IS, Lee JH, Park YS, Shin JI, Lee DY, Kim SY, Choi Y, Cheong HI.
    Nephrol Dial Transplant; 2012 Apr 15; 27(4):1516-21. PubMed ID: 21865213
    [Abstract] [Full Text] [Related]

  • 37. Barttin mutations in antenatal Bartter syndrome with sensorineural deafness.
    Ozlu F, Yapicioğlu H, Satar M, Narli N, Ozcan K, Buyukcelik M, Konrad M, Demirhan O.
    Pediatr Nephrol; 2006 Jul 15; 21(7):1056-7. PubMed ID: 16773427
    [No Abstract] [Full Text] [Related]

  • 38. Novel mutations of the chloride channel Kb gene in two Japanese patients clinically diagnosed as Bartter syndrome with hypocalciuria.
    Fukuyama S, Hiramatsu M, Akagi M, Higa M, Ohta T.
    J Clin Endocrinol Metab; 2004 Nov 15; 89(11):5847-50. PubMed ID: 15531551
    [Abstract] [Full Text] [Related]

  • 39. Bartter syndrome in two sisters with a novel mutation of the CLCNKB gene, one with deafness.
    Robitaille P, Merouani A, He N, Pei Y.
    Eur J Pediatr; 2011 Sep 15; 170(9):1209-11. PubMed ID: 21479528
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