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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

400 related articles for article (PubMed ID: 11025834)

  • 1. Mutation in the gene responsible for cystic fibrosis and predisposition to chronic rhinosinusitis in the general population.
    Wang X; Moylan B; Leopold DA; Kim J; Rubenstein RC; Togias A; Proud D; Zeitlin PL; Cutting GR
    JAMA; 2000 Oct; 284(14):1814-9. PubMed ID: 11025834
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Increased prevalence of chronic rhinosinusitis in carriers of a cystic fibrosis mutation.
    Wang X; Kim J; McWilliams R; Cutting GR
    Arch Otolaryngol Head Neck Surg; 2005 Mar; 131(3):237-40. PubMed ID: 15781764
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Increased prevalence of mutations in the cystic fibrosis transmembrane conductance regulator in children with chronic rhinosinusitis.
    Raman V; Clary R; Siegrist KL; Zehnbauer B; Chatila TA
    Pediatrics; 2002 Jan; 109(1):E13. PubMed ID: 11773581
    [TBL] [Abstract][Full Text] [Related]  

  • 4. The prevalence of CFTR mutations in patients with chronic rhinosinusitis: A systematic review and meta-analysis.
    Yong M; Hernaiz-Leonardo JC; Alqunaee M; Quon BS; Javer A
    Clin Otolaryngol; 2022 Jan; 47(1):24-33. PubMed ID: 34664411
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Paranasal sinus size is decreased in CFTR heterozygotes with chronic rhinosinusitis.
    Calton JB; Koripella PC; Willis AL; Le CH; Chiu AG; Chang EH
    Int Forum Allergy Rhinol; 2017 Mar; 7(3):256-260. PubMed ID: 27860385
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Chronic Rhinosinusitis in Patients with Cystic Fibrosis.
    Hamilos DL
    J Allergy Clin Immunol Pract; 2016; 4(4):605-12. PubMed ID: 27393775
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Application of multiplex ARMS and SSCP/HD analysis in molecular diagnosis of cystic fibrosis in Indian patients.
    Ashavaid TF; Kondkar AA; Dherai AJ; Raghavan R; Udani SV; Udwadia ZF; Desai D
    Mol Diagn; 2005; 9(2):59-66. PubMed ID: 16137181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Correlations between cystic fibrosis genotype and sinus disease severity in chronic rhinosinusitis.
    Abuzeid WM; Song C; Fastenberg JH; Fang CH; Ayoub N; Jerschow E; Mohabir PK; Hwang PH
    Laryngoscope; 2018 Aug; 128(8):1752-1758. PubMed ID: 29193105
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Prospective analysis of cystic fibrosis transmembrane regulator mutations in adults with bronchiectasis or pulmonary nontuberculous mycobacterial infection.
    Ziedalski TM; Kao PN; Henig NR; Jacobs SS; Ruoss SJ
    Chest; 2006 Oct; 130(4):995-1002. PubMed ID: 17035430
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Cystic fibrosis in Korean children:a case report identified by a quantitative pilocarpine iontophoresis sweat test and genetic analysis.
    Ahn KM; Park HY; Lee JH; Lee MG; Kim JH; Kang IJ; Lee SI
    J Korean Med Sci; 2005 Feb; 20(1):153-7. PubMed ID: 15716623
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Genetic diagnosis in practice: From cystic fibrosis to CFTR-related disorders.
    Pagin A; Sermet-Gaudelus I; Burgel PR
    Arch Pediatr; 2020 Feb; 27 Suppl 1():eS25-eS29. PubMed ID: 32172933
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Acid and base secretion in freshly excised nasal tissue from cystic fibrosis patients with ΔF508 mutation.
    Cho DY; Hwang PH; Illek B; Fischer H
    Int Forum Allergy Rhinol; 2011; 1(2):123-7. PubMed ID: 22034590
    [TBL] [Abstract][Full Text] [Related]  

  • 13. CFTR genotype and clinical outcomes of adult patients carried as cystic fibrosis disease.
    Bonadia LC; de Lima Marson FA; Ribeiro JD; Paschoal IA; Pereira MC; Ribeiro AF; Bertuzzo CS
    Gene; 2014 May; 540(2):183-90. PubMed ID: 24583165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Lack of association of common cystic fibrosis transmembrane conductance regulator gene mutations with primary sclerosing cholangitis.
    Gallegos-Orozco JF; E Yurk C; Wang N; Rakela J; Charlton MR; Cutting GR; Balan V
    Am J Gastroenterol; 2005 Apr; 100(4):874-8. PubMed ID: 15784035
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Comparison of radiographic and clinical characteristics of low-risk and high-risk cystic fibrosis genotypes.
    Ferril GR; Nick JA; Getz AE; Barham HP; Saavedra MT; Taylor-Cousar JL; Nichols DP; Curran-Everett D; Kingdom TT; Ramakrishnan VR
    Int Forum Allergy Rhinol; 2014 Nov; 4(11):915-20. PubMed ID: 25224556
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Population-based newborn screening for genetic disorders when multiple mutation DNA testing is incorporated: a cystic fibrosis newborn screening model demonstrating increased sensitivity but more carrier detections.
    Comeau AM; Parad RB; Dorkin HL; Dovey M; Gerstle R; Haver K; Lapey A; O'Sullivan BP; Waltz DA; Zwerdling RG; Eaton RB
    Pediatrics; 2004 Jun; 113(6):1573-81. PubMed ID: 15173476
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Role of CFTR mutation analysis in the diagnostic algorithm for cystic fibrosis.
    Ratkiewicz M; Pastore M; McCoy KS; Thompson R; Hayes D; Sheikh SI
    World J Pediatr; 2017 Apr; 13(2):129-135. PubMed ID: 28194692
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Comprehensive mutation screening in a cystic fibrosis center.
    Wine JJ; Kuo E; Hurlock G; Moss RB
    Pediatrics; 2001 Feb; 107(2):280-6. PubMed ID: 11158459
    [TBL] [Abstract][Full Text] [Related]  

  • 19. [Clinical manifestations and gene analysis of 2 Chinese children with cystic fibrosis].
    Liu JR; Peng Y; Zhao YH; Wang W; Guo Y; He JX; Zhao SY; Jiang ZF
    Zhonghua Er Ke Za Zhi; 2012 Nov; 50(11):829-33. PubMed ID: 23302613
    [TBL] [Abstract][Full Text] [Related]  

  • 20. The cystic fibrosis transmembrane conductance regulator gene and ion channel function in patients with idiopathic pancreatitis.
    Bishop MD; Freedman SD; Zielenski J; Ahmed N; Dupuis A; Martin S; Ellis L; Shea J; Hopper I; Corey M; Kortan P; Haber G; Ross C; Tzountzouris J; Steele L; Ray PN; Tsui LC; Durie PR
    Hum Genet; 2005 Dec; 118(3-4):372-81. PubMed ID: 16193325
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 20.