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PUBMED FOR HANDHELDS

Journal Abstract Search


149 related items for PubMed ID: 10684365

  • 1. Bartter syndrome in a neonate: early treatment with indomethacin.
    Mourani CC, Sanjad SA, Akatcherian CY.
    Pediatr Nephrol; 2000 Feb; 14(2):143-5. PubMed ID: 10684365
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  • 2. Bartter syndrome: presentation in an extremely premature neonate.
    Flores FX, Ojeda FJ, Calhoun DA.
    J Perinatol; 2013 Aug; 33(8):661-2. PubMed ID: 23897314
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  • 3. Hyperprostaglandin E syndrome: use of indomethacin and steroid, and death due to necrotizing enterocolitis and sepsis.
    Cetinkaya M, Köksal N, Ozkan H, Dönmez O, Sağlam H, Kiriştioğlu I.
    Turk J Pediatr; 2008 Aug; 50(4):386-90. PubMed ID: 19014056
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  • 4. [Polyhydramnios, prematurity, dystrophy, polyuria, constipation, nephrocalcinosis and renal tumor: presentation of a classic tubulopathy].
    Schnakenburg Cv, Frankenschmidt A, Neumann J, Häffner K, Jeck N, Pohl M.
    Klin Padiatr; 2008 Aug; 220(1):24-5. PubMed ID: 18172829
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  • 5. A variant of Bartter's syndrome. Bartter's syndrome associated with hydramnios, prematurity, hypercalciuria and nephrocalcinosis.
    Ohlsson A, Sieck U, Cumming W, Akhtar M, Serenius F.
    Acta Paediatr Scand; 1984 Nov; 73(6):868-74. PubMed ID: 6395627
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  • 10. [The neonatal form of Bartter's syndrome: current findings in etiology and physiopathology].
    Proesmans WC.
    Verh K Acad Geneeskd Belg; 1992 Nov; 54(3):253-93. PubMed ID: 1413986
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  • 11. Bartter syndrome: An infrequent tubulopathy of prenatal onset.
    Gómez de la F CL, Novoa P JM, Caviedes R N.
    Rev Chil Pediatr; 2019 Aug; 90(4):437-442. PubMed ID: 31859717
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  • 14. A Rare Disorder with Common Clinical Presentation: Neonatal Bartter Syndrome.
    Hussain S, Tarar SH, Al-Muhaizae M.
    J Coll Physicians Surg Pak; 2015 Apr; 25 Suppl 1():S58-60. PubMed ID: 25933468
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  • 17. Classic Bartter syndrome: a rare cause of failure to thrive in a child.
    Vieira H, Mendes L, Mendes P, da Silva JE.
    BMJ Case Rep; 2012 Jun 28; 2012():. PubMed ID: 22744244
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  • 20. A novel homozygous CLCNKB variant: An early presentation of classic Bartter syndrome in a neonate.
    Yaprak D, Kara H, Calisici E, Karagöl BS, Altan M.
    Birth Defects Res; 2023 Oct 15; 115(17):1674-1679. PubMed ID: 37587715
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