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Journal Abstract Search

262 related items for PubMed ID: 25880437

  • 1. Differential diagnosis of Bartter syndrome, Gitelman syndrome, and pseudo-Bartter/Gitelman syndrome based on clinical characteristics.
    Matsunoshita N, Nozu K, Shono A, Nozu Y, Fu XJ, Morisada N, Kamiyoshi N, Ohtsubo H, Ninchoji T, Minamikawa S, Yamamura T, Nakanishi K, Yoshikawa N, Shima Y, Kaito H, Iijima K.
    Genet Med; 2016 Feb; 18(2):180-8. PubMed ID: 25880437
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  • 2. Congenital chloride diarrhea needs to be distinguished from Bartter and Gitelman syndrome.
    Matsunoshita N, Nozu K, Yoshikane M, Kawaguchi A, Fujita N, Morisada N, Ishimori S, Yamamura T, Minamikawa S, Horinouchi T, Nakanishi K, Fujimura J, Ninchoji T, Morioka I, Nagase H, Taniguchi-Ikeda M, Kaito H, Iijima K.
    J Hum Genet; 2018 Jul; 63(8):887-892. PubMed ID: 29849040
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  • 3. Inherited salt-losing tubulopathy: An old condition but a new category of tubulopathy.
    Nozu K, Yamamura T, Horinouchi T, Nagano C, Sakakibara N, Ishikura K, Hamada R, Morisada N, Iijima K.
    Pediatr Int; 2020 Apr; 62(4):428-437. PubMed ID: 31830341
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  • 4. A thiazide test for the diagnosis of renal tubular hypokalemic disorders.
    Colussi G, Bettinelli A, Tedeschi S, De Ferrari ME, Syrén ML, Borsa N, Mattiello C, Casari G, Bianchetti MG.
    Clin J Am Soc Nephrol; 2007 May; 2(3):454-60. PubMed ID: 17699451
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  • 5. Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia.
    Bao M, Cai J, Yang X, Ma W.
    Clin Exp Hypertens; 2019 May; 41(4):381-388. PubMed ID: 29953267
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  • 6. Urinary exosomes in the diagnosis of Gitelman and Bartter syndromes.
    Corbetta S, Raimondo F, Tedeschi S, Syrèn ML, Rebora P, Savoia A, Baldi L, Bettinelli A, Pitto M.
    Nephrol Dial Transplant; 2015 Apr; 30(4):621-30. PubMed ID: 25422309
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  • 7. Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome.
    Palazzo V, Raglianti V, Landini S, Cirillo L, Errichiello C, Buti E, Artuso R, Tiberi L, Vergani D, Dirupo E, Romagnani P, Mazzinghi B, Becherucci F.
    Int J Mol Sci; 2022 May 18; 23(10):. PubMed ID: 35628451
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  • 9. Myocardial perfusion defects in Bartter and Gitelman syndromes.
    Scognamiglio R, Calò LA, Negut C, Coccato M, Mormino P, Pessina AC.
    Eur J Clin Invest; 2008 Dec 18; 38(12):888-95. PubMed ID: 19021712
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  • 12. Different roles of the RAAS affect bone metabolism in patients with primary aldosteronism, Gitelman syndrome and Bartter syndrome.
    Tang W, Chai Y, Jia H, Wang B, Liu T, Wang H, Dai C.
    BMC Endocr Disord; 2022 Feb 11; 22(1):38. PubMed ID: 35148746
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  • 14. [Bartter-Gitelman syndromes].
    Blanchard A, Courand PY, Livrozet M, Vargas-Poussou R.
    Nephrol Ther; 2020 Jul 11; 16(4):233-243. PubMed ID: 32622651
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  • 15. Gitelman or Bartter type 3 syndrome? A case of distal convoluted tubulopathy caused by CLCNKB gene mutation.
    Cruz AJ, Castro A.
    BMJ Case Rep; 2013 Jan 22; 2013():. PubMed ID: 23345488
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  • 16. A novel mutation in the chloride channel gene, CLCNKB, as a cause of Gitelman and Bartter syndromes.
    Zelikovic I, Szargel R, Hawash A, Labay V, Hatib I, Cohen N, Nakhoul F.
    Kidney Int; 2003 Jan 22; 63(1):24-32. PubMed ID: 12472765
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  • 19. Adult classic Bartter syndrome: a case report with 5-year follow-up and literature review.
    Jiang L, Li D, Guo Q, Li Y, Zan L, Ao R.
    Endocr J; 2024 May 23; 71(5):537-542. PubMed ID: 38508775
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  • 20. Hypokalaemia and failure to thrive: report of a misleading onset.
    Conti G, Vitale A, Tedeschi S, Syrén ML, Pantano R, Chimenz R, Fede S, La Torre F, Coviello D, Fede C.
    J Paediatr Child Health; 2010 May 23; 46(5):276-7. PubMed ID: 20412406
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