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.


PUBMED FOR HANDHELDS

Journal Abstract Search


164 related items for PubMed ID: 9050094

  • 1. Is nasal polyposis in cystic fibrosis a direct manifestation of genetic mutation or a complication of chronic infection?
    De Gaudemar I, Contencin P, Van den Abbeele T, Munck A, Navarro J, Narcy P.
    Rhinology; 1996 Dec; 34(4):194-7. PubMed ID: 9050094
    [Abstract] [Full Text] [Related]

  • 2. Nasal and paranasal sinus endoscopy, computed tomography and microbiology of upper airways and the correlations with genotype and severity of cystic fibrosis.
    Sakano E, Ribeiro AF, Barth L, Condino Neto A, Ribeiro JD.
    Int J Pediatr Otorhinolaryngol; 2007 Jan; 71(1):41-50. PubMed ID: 17007941
    [Abstract] [Full Text] [Related]

  • 3. Familial concordance of phenotype and microbial variation among siblings with CF.
    Picard E, Aviram M, Yahav Y, Rivlin J, Blau H, Bentur L, Avital A, Villa Y, Schwartz S, Kerem B, Kerem E.
    Pediatr Pulmonol; 2004 Oct; 38(4):292-7. PubMed ID: 15334505
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 5. Histology of nasal polyps of different etiology.
    Sorensen H, Mygind N, Tygstrup I, Winge Flensborg E.
    Rhinology; 1977 Sep; 15(3):121-8. PubMed ID: 905718
    [Abstract] [Full Text] [Related]

  • 6. Rhinosinusitis in cystic fibrosis: not a simple story.
    Babinski D, Trawinska-Bartnicka M.
    Int J Pediatr Otorhinolaryngol; 2008 May; 72(5):619-24. PubMed ID: 18294702
    [Abstract] [Full Text] [Related]

  • 7. [Correlation between phenotype and genotype in a group of patients with cystic fibrosis].
    Navarro H, Kolbach M, Repetto G, Guiraldes E, Harris P, Foradori A, Poggi H, Sánchez I.
    Rev Med Chil; 2002 May; 130(5):475-81. PubMed ID: 12143267
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Relations between the frequency of the DeltaF 508 mutation and the course of pulmonary disease in cystic fibrosis patients infected with Pseudomonas aeruginosa.
    Rosenecker J.
    Eur J Med Res; 2000 Aug 18; 5(8):356-9. PubMed ID: 10958769
    [Abstract] [Full Text] [Related]

  • 10. Priming of blood neutrophils in children with cystic fibrosis: correlation between functional and phenotypic expression of opsonin receptors before and after platelet-activating factor priming.
    Witko-Sarsat V, Halbwachs-Mecarelli L, Sermet-Gaudelus I, Bessou G, Lenoir G, Allen RC, Descamps-Latscha B.
    J Infect Dis; 1999 Jan 18; 179(1):151-62. PubMed ID: 9841834
    [Abstract] [Full Text] [Related]

  • 11. [Rhinosinusal manifestations of cystic fibrosis].
    Triglia JM, Belus JF, Dessi P, Noirclerc M, Cannoni M.
    Ann Otolaryngol Chir Cervicofac; 1993 Jan 18; 110(2):98-102. PubMed ID: 8363304
    [Abstract] [Full Text] [Related]

  • 12. Pulmonary infection in mild variant cystic fibrosis: implications for care.
    Lording A, McGaw J, Dalton A, Beal G, Everard M, Taylor CJ.
    J Cyst Fibros; 2006 May 18; 5(2):101-4. PubMed ID: 16426904
    [Abstract] [Full Text] [Related]

  • 13. 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 18; 3(4):259-63. PubMed ID: 15698945
    [Abstract] [Full Text] [Related]

  • 14. [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 Dec 18; 129 Suppl 1():6-9. PubMed ID: 15637983
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17. The 3849 + 10 kB C-->T mutation in a 21-year-old patient with cystic fibrosis.
    Kaplan DM, Niv A, Aviram M, Parvari R, Leiberman A, Fliss DM.
    Ear Nose Throat J; 1996 Dec 18; 75(12):793-5. PubMed ID: 8991230
    [Abstract] [Full Text] [Related]

  • 18. Infections with Pseudomonas aeruginosa in patients with cystic fibrosis.
    Tümmler B, Bosshammer J, Breitenstein S, Brockhausen I, Gudowius P, Herrmann C, Herrmann S, Heuer T, Kubesch P, Mekus F, Römling U, Schmidt KD, Spangenberg C, Walter S.
    Behring Inst Mitt; 1997 Feb 18; (98):249-55. PubMed ID: 9382747
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20. Aquagenic wrinkling of the palms in cystic fibrosis: comparison with controls and genotype-phenotype correlations.
    Berk DR, Ciliberto HM, Sweet SC, Ferkol TW, Bayliss SJ.
    Arch Dermatol; 2009 Nov 18; 145(11):1296-9. PubMed ID: 19917960
    [Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 9.