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Journal Abstract Search

147 related items for PubMed ID: 9628826

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  • 2. Fifteen-year follow-up of pulmonary function in individuals heterozygous for the cystic fibrosis phenylalanine-508 deletion.
    Dahl M, Nordestgaard BG, Lange P, Tybjaerg-Hansen A.
    J Allergy Clin Immunol; 2001 May; 107(5):818-23. PubMed ID: 11344348
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  • 3. No association between the deltaF508 cystic fibrosis mutation and type 2 diabetes mellitus.
    Braun J, Arnemann J, Lohrey M, Donner H, Siegmund T, Usadel KH, Badenhoop K.
    Exp Clin Endocrinol Diabetes; 1999 May; 107(8):568-9. PubMed ID: 10612489
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  • 4. [Genotype and phenotype of gastrointestinal symptoms analysis in children with cystic fibrosis].
    Iwańczak F, Smigiel R, Stawarski A, Pawłowicz J, Stembalska A, Mowszet K, Sasiadek M.
    Pol Merkur Lekarski; 2005 Feb; 18(104):205-9. PubMed ID: 17877132
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  • 6. Genotype-phenotype relationship for five CFTR mutations frequently identified in western France.
    Duguépéroux I, De Braekeleer M, Participating Centres to the French National Cystic Fibrosis Registry.
    J Cyst Fibros; 2004 Dec; 3(4):259-63. PubMed ID: 15698945
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  • 7. Pancreatic function and extended mutation analysis in DeltaF508 heterozygous infants with an elevated immunoreactive trypsinogen but normal sweat electrolyte levels.
    Massie RJ, Wilcken B, Van Asperen P, Dorney S, Gruca M, Wiley V, Gaskin K.
    J Pediatr; 2000 Aug; 137(2):214-20. PubMed ID: 10931414
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  • 8. Glucose homeostasis and genotype-phenotype interplay in cystic fibrosis patients with CFTR gene deltaF508 mutation.
    Preumont V, Hermans MP, Lebecque P, Buysschaert M.
    Diabetes Care; 2007 May; 30(5):1187-92. PubMed ID: 17337503
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  • 9. Population screening of F508del (DeltaF508), the most frequent mutation in the CFTR gene associated with cystic fibrosis in Argentina.
    Roqué M, Godoy CP, Castellanos M, Pusiol E, Mayorga LS.
    Hum Mutat; 2001 Aug; 18(2):167. PubMed ID: 11462248
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  • 10. Frequency and clinical significance of the S1235R mutation in the cystic fibrosis transmembrane conductance regulator gene: results from a collaborative study.
    Monaghan KG, Feldman GL, Barbarotto GM, Manji S, Desai TK, Snow K.
    Am J Med Genet; 2000 Dec 11; 95(4):361-5. PubMed ID: 11186891
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  • 12. [Frequency of delta F508 mutation in Venezuelan patients with cystic fibrosis].
    Morales-Machin A, Borjas-Fajardo L, Pineda L, González S, Delgado W, Zabala W, Fernández E.
    Invest Clin; 2004 Jun 11; 45(2):121-30. PubMed ID: 15211979
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  • 13. Cystic fibrosis heterozygotes do not have increased platelet activation.
    Tarnow I, Michelson AD, Frelinger AL, Linden MD, Li Y, Fox ML, Barnard MR, O'Sullivan BP.
    Thromb Res; 2007 Jun 11; 121(2):159-62. PubMed ID: 17532368
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  • 17. The DeltaF508 mutation in Ecuador, South America.
    Paz-y-Miño C, Pérez JC, Burgos R, Dávalos MV, Leone PE.
    Hum Mutat; 1999 Jun 11; 14(4):348-50. PubMed ID: 10502783
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