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101 related items for PubMed ID: 15357568

  • 1. Pseudo-Bartter's syndrome in an Egyptian infant with cystic fibrosis mutation N1303K.
    Wahab AA, Janahi IA, Marafia MM.
    J Trop Pediatr; 2004 Aug; 50(4):242-4. PubMed ID: 15357568
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  • 2. Analysis of the CFTR gene in Iranian cystic fibrosis patients: identification of eight novel mutations.
    Alibakhshi R, Kianishirazi R, Cassiman JJ, Zamani M, Cuppens H.
    J Cyst Fibros; 2008 Mar; 7(2):102-9. PubMed ID: 17662673
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  • 3. Mutation analysis of CFTR gene in 70 Iranian cystic fibrosis patients.
    Alibakhshi R, Zamani M.
    Iran J Allergy Asthma Immunol; 2006 Mar; 5(1):3-8. PubMed ID: 17242497
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  • 4. Cystic fibrosis detection in high-risk Egyptian children and CFTR mutation analysis.
    Naguib ML, Schrijver I, Gardner P, Pique LM, Doss SS, Abu Zekry MA, Aziz M, Nasr SZ.
    J Cyst Fibros; 2007 Apr; 6(2):111-6. PubMed ID: 16837250
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  • 5. Pseudo-Bartter's syndrome revealing cystic fibrosis in an infant caused by 3849 + 1G>A and 4382delA compound heterozygosity.
    Nahida el-R, Mohammed H, Guy L.
    Acta Paediatr; 2011 Nov; 100(11):e234-5. PubMed ID: 21449922
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  • 7. 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
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  • 10. Segregation analysis in cystic fibrosis at-risk family demonstrates that the M348K CFTR mutation is a rare innocuous polymorphism.
    D'Apice MR, Gambardella S, Russo S, Lucidi V, Nardone AM, Pietropolli A, Novelli G.
    Prenat Diagn; 2004 Dec 15; 24(12):981-3. PubMed ID: 15614862
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  • 11. [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 15; 18(104):205-9. PubMed ID: 17877132
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  • 12. Common mutations in Cuban cystic fibrosis patients.
    Collazo T, Bofill AM, Clark Y, Hernández Y, Gómez M, Rodríguez F, Ramos MD, Giménez J, Casals T, Rojo M.
    J Cyst Fibros; 2009 Jan 15; 8(1):47-9. PubMed ID: 18938114
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  • 13. [Relation between gene mutations and pancreatic exocrine function in patients with cystic fibrosis].
    Radivojević D, Guć-Sćekić M, Djurisić M, Lalić T, Minić P, Kanavakis E.
    Srp Arh Celok Lek; 2001 Jan 15; 129 Suppl 1():6-9. PubMed ID: 15637983
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  • 20. The changing face of the exocrine pancreas in cystic fibrosis: the correlation between pancreatic status, pancreatitis and cystic fibrosis genotype.
    Augarten A, Ben Tov A, Madgar I, Barak A, Akons H, Laufer J, Efrati O, Aviram M, Bentur L, Blau H, Paret G, Wilschanski M, Kerem BS, Yahav Y.
    Eur J Gastroenterol Hepatol; 2008 Mar 15; 20(3):164-8. PubMed ID: 18301294
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