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3. Pseudo-Bartter syndrome as the sole manifestation of cystic fibrosis in a child with 711+G>T/IVS8-5T mutation: a new face of an old disease. Tinsa F, Hadj Fredj S, Bel Hadj I, Khalsi F, Abdelhak S, Boussetta K, Messaoud T. Ann Biol Clin (Paris); 2017 Aug 01; 75(4):466-473. PubMed ID: 28751295 [Abstract] [Full Text] [Related]
4. A Novel Mutation in Cystic Fibrosis Presenting as Pseudo Bartter Syndrome: A Case Report. Shah S, Jondhale S, Sahoo MR, Jagzape T, Keshri S, Goel AK. Indian J Clin Biochem; 2023 Oct 01; 38(4):550-552. PubMed ID: 37746536 [Abstract] [Full Text] [Related]
5. Atypical presentation of cystic fibrosis--obese adolescent with hypertension and pseudo-Bartter's syndrome. Sovtić A, Minić P, Bogdanović R, Stajić N, Rodić M, Marković-Sovtić G. Vojnosanit Pregl; 2012 Apr 01; 69(4):367-9. PubMed ID: 22624431 [Abstract] [Full Text] [Related]
6. [Pseudo-Bartter syndrome in a case of cystic fibrosis caused by C1529G and G3978A compound heterozygosity]. Horvatovich K, Orkényi M, Bíró E, Pongrácz K, Kisfali P, Talián G, Csöngei V, Járomi L, Sáfrány E, Harangi F, Sulyok E, Melegh B. Orv Hetil; 2008 Feb 17; 149(7):325-8. PubMed ID: 18258563 [Abstract] [Full Text] [Related]
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9. [Dehydration and metabolic alkalosis: an unusual presentation of cystic fibrosis in an infant]. Aranzamendi RJ, Breitman F, Asciutto C, Delgado N, Castaños C. Arch Argent Pediatr; 2008 Oct 17; 106(5):443-6. PubMed ID: 19030645 [Abstract] [Full Text] [Related]
12. [Turkish infant with hypoelectrolytemia and metabolic alkalosis as the sole manifestations of a mild form of cystic fibrosis (mutation D110H)]. Weller F, Wiebicke W, Tümmler B. Klin Padiatr; 2000 Oct 17; 212(1):41-3. PubMed ID: 10719683 [Abstract] [Full Text] [Related]