These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
64. Prognostic value of sweat-chloride levels in cystic fibrosis: a negative report. Corkey CW; Corey M; Gaskin K; Levison H Eur J Respir Dis; 1983 Aug; 64(6):434-6. PubMed ID: 6884456 [TBL] [Abstract][Full Text] [Related]
65. New diagnostic method for cystic fibrosis. Taylor CJ; Baxter PS; Dickson J; Hardcastle J; Hardcastle PT; Goldhill J Acta Univ Carol Med (Praha); 1990; 36(1-4):142-3. PubMed ID: 2130677 [TBL] [Abstract][Full Text] [Related]
66. Successful pregnancy in a female patient with congenital chloride diarrhea (CLD) and renal impairment. Shimizu Y; Kamoda T; Nagata M; Yoh K; Hashimoto Y; Matsui A; Yoshikawa H; Yamagata K; Koyama A J Nephrol; 2009; 22(6):809-13. PubMed ID: 19967661 [TBL] [Abstract][Full Text] [Related]
67. [Long term treatment results for chloride diarrhea]. Kierkuś J; Socha P; Popińska K; Socha J Wiad Lek; 1995; 48(1-12):203-5. PubMed ID: 9638241 [No Abstract] [Full Text] [Related]
68. N1303K and IVS8-5T, clinical presentation within a family with atypical cystic fibrosis. Van Hoorenbeeck K; Storm K; van den Ende J; Biervliet M; Desager KN J Cyst Fibros; 2007 May; 6(3):220-2. PubMed ID: 17127107 [TBL] [Abstract][Full Text] [Related]
69. The clinical and laboratory manifestations of Iranian patients with cystic fibrosis. Fallahi G; Najafi M; Farhmand F; Bazvand F; Ahmadi M; Ahmadi F; Eftekhari K; Khodad A; Motamed F; Khatami G; Aghamohammadi A; Rezaei N Turk J Pediatr; 2010; 52(2):132-8. PubMed ID: 20560247 [TBL] [Abstract][Full Text] [Related]
70. SLC26A3 mutations in congenital chloride diarrhea. Mäkelä S; Kere J; Holmberg C; Höglund P Hum Mutat; 2002 Dec; 20(6):425-38. PubMed ID: 12442266 [TBL] [Abstract][Full Text] [Related]
72. A novel homozygous SLC26A3 nonsense mutation in a Tyrolean girl with congenital chloride diarrhea. Heinz-Erian P; Oberauer M; Neu N; Müller T; Scholl-Bürgi S; Hager J; Pittschieler K; Janecke AR J Pediatr Gastroenterol Nutr; 2008 Sep; 47(3):363-6. PubMed ID: 18728535 [No Abstract] [Full Text] [Related]
73. Congenital chloridorrhoea in two Korean infants. Lee HJ; Lee KJ; Seo JK; Moon HR J Inherit Metab Dis; 1994; 17(1):126-30. PubMed ID: 8051922 [No Abstract] [Full Text] [Related]
74. Mutations in the chloride channel gene, CLCNKB, leading to a mixed Bartter-Gitelman phenotype. Jeck N; Konrad M; Peters M; Weber S; Bonzel KE; Seyberth HW Pediatr Res; 2000 Dec; 48(6):754-8. PubMed ID: 11102542 [TBL] [Abstract][Full Text] [Related]