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Journal Abstract Search

182 related items for PubMed ID: 1843056

  • 1. Cystic fibrosis in Japan.
    Kunitomo K, Komi N, Kawahito M, Miura M, Sasaki K.
    Tokushima J Exp Med; 1991 Dec; 38(3-4):85-9. PubMed ID: 1843056
    [Abstract] [Full Text] [Related]

  • 2. Molecular diagnosis of cystic fibrosis in Indian patients--a preliminary report.
    Ashavaid TF, Dherai AJ, Kondkar AA, Raghavan R, Udani SV, Udwadia ZF, Desai D.
    J Assoc Physicians India; 2003 Apr; 51():345-8. PubMed ID: 12723646
    [Abstract] [Full Text] [Related]

  • 3. Cystic fibrosis in Ontario.
    Sturgess JM, Czegledy-Nagy E, Corey M, Thompson MW.
    Am J Med Genet; 1985 Oct; 22(2):383-93. PubMed ID: 4050869
    [Abstract] [Full Text] [Related]

  • 4. Sweat conductivity and chloride titration for cystic fibrosis diagnosis in 3834 subjects.
    Lezana JL, Vargas MH, Karam-Bechara J, Aldana RS, Furuya ME.
    J Cyst Fibros; 2003 Mar; 2(1):1-7. PubMed ID: 15463838
    [Abstract] [Full Text] [Related]

  • 5.
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  • 6. Borderline sweat test: Utility and limits of genetic analysis for the diagnosis of cystic fibrosis.
    Seia M, Costantino L, Paracchini V, Porcaro L, Capasso P, Coviello D, Corbetta C, Torresani E, Magazzù D, Consalvo V, Monti A, Costantini D, Colombo C.
    Clin Biochem; 2009 May; 42(7-8):611-6. PubMed ID: 19318035
    [Abstract] [Full Text] [Related]

  • 7. Sweat electrolyte and cystic fibrosis mutation analysis allows early diagnosis in Brazilian children with clinical signs compatible with cystic fibrosis.
    Rabbi-Bortolini E, Bernardino AL, Lopes AL, Ferri AS, Passos-Bueno MR, Zatz M.
    Am J Med Genet; 1998 Apr 01; 76(4):288-90. PubMed ID: 9545091
    [Abstract] [Full Text] [Related]

  • 8. [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 01; 130(5):475-81. PubMed ID: 12143267
    [Abstract] [Full Text] [Related]

  • 9. Cystic fibrosis mutations with widely variable phenotype: the D1152H example.
    Mussaffi H, Prais D, Mei-Zahav M, Blau H.
    Pediatr Pulmonol; 2006 Mar 01; 41(3):250-4. PubMed ID: 16429425
    [Abstract] [Full Text] [Related]

  • 10. [A case report of cystic fibrosis and review of 16 cases of cystic fibrosis in Chinese patients].
    Li N, He B, Wang GF, Tang XY.
    Zhonghua Jie He He Hu Xi Za Zhi; 2003 Sep 01; 26(9):559-62. PubMed ID: 14521762
    [Abstract] [Full Text] [Related]

  • 11. Conductivity determined by a new sweat analyzer compared with chloride concentrations for the diagnosis of cystic fibrosis.
    Barben J, Ammann RA, Metlagel A, Schoeni MH, Swiss Paediatric Respiratory Research Group.
    J Pediatr; 2005 Feb 01; 146(2):183-8. PubMed ID: 15689903
    [Abstract] [Full Text] [Related]

  • 12. The clinical and laboratory manifestations of Iranian patients with cystic fibrosis.
    Fallahi G, Najafi M, Farhmand F, Bazvand F, Ahmadi M, Ahmadi F, Eftekhari K, Khodad A, Motamed F, Khatami G, Aghamohammadi A, Rezaei N.
    Turk J Pediatr; 2010 Feb 01; 52(2):132-8. PubMed ID: 20560247
    [Abstract] [Full Text] [Related]

  • 13. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K, Weren M, Proesmans M, Kerem E.
    Pediatrics; 2005 Apr 01; 115(4):e463-9. PubMed ID: 15772171
    [Abstract] [Full Text] [Related]

  • 14. Diagnosis of cystic fibrosis by sweat testing: age-specific reference intervals.
    Mishra A, Greaves R, Smith K, Carlin JB, Wootton A, Stirling R, Massie J.
    J Pediatr; 2008 Dec 01; 153(6):758-63. PubMed ID: 18589442
    [Abstract] [Full Text] [Related]

  • 15. [Clinical characteristics and outcome of cystic fibrosis: report of 16 cases].
    Khemiri M, Ben Rhouma A, Bouzid S, Messaoud T, Guesmi M, Hamzaoui M, Fattoum S, Khaldi F, Barsaoui S.
    Tunis Med; 2008 Jun 01; 86(6):567-72. PubMed ID: 19216450
    [Abstract] [Full Text] [Related]

  • 16. Infant care patterns at epidemiologic study of cystic fibrosis sites that achieve superior childhood lung function.
    Padman R, McColley SA, Miller DP, Konstan MW, Morgan WJ, Schechter MS, Ren CL, Wagener JS, Investigators and Coordinators of the Epidemiologic Study of Cystic Fibrosis.
    Pediatrics; 2007 Mar 01; 119(3):e531-7. PubMed ID: 17332172
    [Abstract] [Full Text] [Related]

  • 17. [Cystic fibrosis of the child].
    Chaabouni M, Krichen A, Ben Halima N, Aloulou H, Mahfoudh A, Hachicha M, Messoud T, Fattoum S, Triki A, Karray A.
    Tunis Med; 2004 Jun 01; 82(6):516-25. PubMed ID: 15517950
    [Abstract] [Full Text] [Related]

  • 18. The CF-CIRC study: a French collaborative study to assess the accuracy of cystic fibrosis diagnosis in neonatal screening.
    Sermet-Gaudelus I, Roussel D, Bui S, Deneuville E, Huet F, Reix P, Bellon G, Lenoir G, Edelman A.
    BMC Pediatr; 2006 Oct 03; 6():25. PubMed ID: 17018149
    [Abstract] [Full Text] [Related]

  • 19. Negative effects of oral fatty acid supplementation on sweat chloride in cystic fibrosis.
    Lloyd-Still JD, Simon SH, Wessel HU, Gibson LE.
    Pediatrics; 1979 Jul 03; 64(1):50-2. PubMed ID: 450561
    [Abstract] [Full Text] [Related]

  • 20. [Clinical heterogeneity at the diagnosis in a cystic fibrosis population].
    Lucidi V, Rosati P, Bella S, Papadatou B, Ferretti F, Orrù M, Diámanti A, Castro M.
    Pediatr Med Chir; 1995 Jul 03; 17(1):57-9. PubMed ID: 7739929
    [Abstract] [Full Text] [Related]

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