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Last Posted: May 07, 2020

• Clinical features and accompanying findings of Pseudo-Bartter Syndrome in cystic fibrosis.
  Sismanlar Eyuboglu Tugba et al. Pediatric pulmonology 2020 May
• Cystic fibrosis in Turkey: First data from the national registry.
  Dogru Deniz et al. Pediatric pulmonology 2019 Nov
• The utility of next generation sequencing in the correct diagnosis of congenital hypochloremic hypokalemic metabolic alkalosis.
  Ben-David Yael et al. European journal of medical genetics 2019 Jul 103728
• Phenotypic spectrum and genetic heterogeneity of cystic fibrosis in Sri Lanka.
  Indika Neluwa Liyanage Ruwan et al. BMC medical genetics 2019 May 20(1) 89
• Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis.
  Najafi Maryam et al. Orphanet journal of rare diseases 2019 Feb 14(1) 41
• Genetic screening for Bartter syndrome and Gitelman syndrome pathogenic genes among individuals with hypertension and hypokalemia.
  Bao Minghui et al. Clinical and experimental hypertension (New York, N.Y. : 1993) 2018 Jun 1-8
• Bartter syndrome
  From NCATS Genetic and Rare Diseases Information Center
• Bartter syndrome antenatal type 1
  From NCATS Genetic and Rare Diseases Information Center
• Bartter syndrome antenatal type 2
  From NCATS Genetic and Rare Diseases Information Center
• Bartter syndrome type 3
  From NCATS Genetic and Rare Diseases Information Center

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