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2. [New therapeutic modalities for pulmonary disease in cystic fibrosis]. Virgilis D; Augarten A; Szeinberg A; Yahav Y Harefuah; 1995 Dec; 129(12):569-72. PubMed ID: 8682360 [No Abstract] [Full Text] [Related]
3. The amiloride-inhibitable Na+ conductance is reduced by the cystic fibrosis transmembrane conductance regulator in normal but not in cystic fibrosis airways. Mall M; Bleich M; Greger R; Schreiber R; Kunzelmann K J Clin Invest; 1998 Jul; 102(1):15-21. PubMed ID: 9649552 [TBL] [Abstract][Full Text] [Related]
4. [Cystic fibrosis: from the child to the adult]. Murris-Espin M; Didier A Rev Mal Respir; 2000 Aug; 17(3 Pt 2):721-3. PubMed ID: 11076381 [No Abstract] [Full Text] [Related]
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15. Homozygosity for L997F in a child with normal clinical and chloride secretory phenotype provides evidence that this cystic fibrosis transmembrane conductance regulator mutation does not cause cystic fibrosis. Derichs N; Schuster A; Grund I; Ernsting A; Stolpe C; Körtge-Jung S; Gallati S; Stuhrmann M; Kozlowski P; Ballmann M Clin Genet; 2005 Jun; 67(6):529-31. PubMed ID: 15857421 [No Abstract] [Full Text] [Related]
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17. [From gene to disease; from defective chloride ion transport to cystic fibrosis]. Scheffer H; van den Ouweland AM; Veeze HJ Ned Tijdschr Geneeskd; 2001 Apr; 145(14):686-7. PubMed ID: 11530706 [TBL] [Abstract][Full Text] [Related]