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Journal Abstract Search
146 related items for PubMed ID: 20981452
1. Hypochloremic metabolic alkalosis and failure to thrive: answer. Querfeld U, Lechner S, Janecke AR. Pediatr Nephrol; 2011 Jun; 26(6):895-6. PubMed ID: 20981452 [No Abstract] [Full Text] [Related]
2. Hypochloremic metabolic alkalosis and failure to thrive: question. Querfeld U, Lechner S, Janecke AR. Pediatr Nephrol; 2011 Jun; 26(6):893. PubMed ID: 20981453 [No Abstract] [Full Text] [Related]
3. Congenital chloride diarrhea misdiagnosed as Bartter syndrome. Eğrıtaş O, Dalgiç B, Wedenoja S. Turk J Gastroenterol; 2011 Jun; 22(3):321-3. PubMed ID: 21805424 [Abstract] [Full Text] [Related]
4. Congenital chloride diarrhea presenting in newborn as a rare cause of meconium ileus. Shamaly H, Jamalia J, Omari H, Shalev S, Elias N. J Perinatol; 2013 Feb; 33(2):154-6. PubMed ID: 23361499 [Abstract] [Full Text] [Related]
5. 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 [Abstract] [Full Text] [Related]
6. Diagnostic Challenge of Congenital Chloride Diarrhea and Ulcerative Colitis Overlap in an Adult Misdiagnosed with Bartter Syndrome: Case Report and Literature Review. Sadagah LF, Makeen AZ, Kotbi ET. Am J Case Rep; 2022 Jul 05; 23():e936715. PubMed ID: 35787602 [Abstract] [Full Text] [Related]
7. Pseudo-Bartter syndrome in an infant with congenital chloride diarrhoea. Igrutinović Z, Peco-Antić A, Radlović N, Vuletić B, Marković S, Vujić A, Rasković Z. Srp Arh Celok Lek; 2011 Jul 05; 139(9-10):677-80. PubMed ID: 22070007 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
12. Congenital chloride diarrhoea in a Chinese infant with a compound heterozygous SLC26A3 mutation. Li Q, Wang J, Zang R, Yu L, Yang Z, Sun S. BMC Pediatr; 2024 May 04; 24(1):305. PubMed ID: 38704545 [Abstract] [Full Text] [Related]
13. Congenital chloride diarrhoea. Sajid A, Riaz S, Riaz A, Safdar B. BMJ Case Rep; 2019 Dec 10; 12(12):. PubMed ID: 31826900 [Abstract] [Full Text] [Related]
16. A Turkish case of congenital chloride diarrhea with SLC26A3 gene (c.2025_2026insATC) mutation: diagnostic pitfalls. Özbay Hoşnut F, Karadağ Öncel E, Öncel MY, Özcay F. Turk J Gastroenterol; 2010 Dec 10; 21(4):443-7. PubMed ID: 21332001 [Abstract] [Full Text] [Related]
17. Congenital Chloride Diarrhea - Novel Mutation in SLC26A3 Gene. Bhardwaj S, Pandit D, Sinha A, Hari P, Cheong HI, Bagga A. Indian J Pediatr; 2016 Aug 10; 83(8):859-61. PubMed ID: 26637435 [Abstract] [Full Text] [Related]