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 *

110 related articles for article (PubMed ID: 9017943)

  • 1. The diagnosis of cystic fibrosis.
    Stern RC
    N Engl J Med; 1997 Feb; 336(7):487-91. PubMed ID: 9017943
    [No Abstract]   [Full Text] [Related]  

  • 2. Congenital bilateral absence of vas deferens in absence of cystic fibrosis.
    Dumur V; Gervais R; Rigot JM; Delomel-Vinner E; Lafitte JJ; Roussel P
    Lancet; 1995 Jan; 345(8943):200-1. PubMed ID: 7823702
    [No Abstract]   [Full Text] [Related]  

  • 3. Diagnostic criteria for cystic fibrosis in men with congenital absence of the vas deferens.
    Durieu I; Bey-Omar F; Rollet J; Calemard L; Boggio D; Lejeune H; Gilly R; Morel Y; Durand DV
    Medicine (Baltimore); 1995 Jan; 74(1):42-7. PubMed ID: 7837969
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Congenital absence of vas deferens and cystic fibrosis.
    Leonardi S; Bombace V; Rotolo N; Sciuto C; La Rosa M
    Minerva Pediatr; 2003 Feb; 55(1):43-7, 47-50. PubMed ID: 12660625
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Cystic fibrosis presenting with haematological abnormalities.
    Minasian CC; Sriskandan S; Balfour-Lynn IM; Bush A
    Clin Lab Haematol; 2006 Dec; 28(6):423-6. PubMed ID: 17105498
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutations in CFTR gene and clinical correlation in Argentine patients with congenital bilateral absence of the vas deferens.
    Levy EM; Granados P; Rawe V; Olmedo SB; Luna MC; Cafferata E; Pivetta OH
    Medicina (B Aires); 2004; 64(3):213-8. PubMed ID: 15239534
    [TBL] [Abstract][Full Text] [Related]  

  • 7. [A study evaluating the correlation between the phenotype and genotype among 65 cystic fibrosis patients].
    Nowakowska A; Bal J; Obersztyn E; Sands D; Maciejko D; Mazurczak T
    Pediatr Pol; 1995 Aug; 70(8):633-8. PubMed ID: 8668363
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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; 76(4):288-90. PubMed ID: 9545091
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Normal sweat chloride values do not exclude the diagnosis of cystic fibrosis.
    Pignatti PF; Luisetti M
    Am J Respir Crit Care Med; 1995 Nov; 152(5 Pt 1):1736-7. PubMed ID: 7582320
    [No Abstract]   [Full Text] [Related]  

  • 10. Molecular screening of CFTR gene in Brazilian men with bilateral agenesis of the vas deferens.
    Bertuzzo CS; Pinto W
    Hum Fertil (Camb); 2006 Mar; 9(1):53-6. PubMed ID: 16581722
    [TBL] [Abstract][Full Text] [Related]  

  • 11. A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations.
    Highsmith WE; Burch LH; Zhou Z; Olsen JC; Boat TE; Spock A; Gorvoy JD; Quittel L; Friedman KJ; Silverman LM
    N Engl J Med; 1994 Oct; 331(15):974-80. PubMed ID: 7521937
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 13. An approach to selection of atypical cystic fibrosis clinical phenotypes.
    Ganev V; Tzoneva M; Tzvetkov D
    Acta Univ Carol Med (Praha); 1990; 36(1-4):247-9. PubMed ID: 2130711
    [No Abstract]   [Full Text] [Related]  

  • 14. The relation between genotype and phenotype in cystic fibrosis--analysis of the most common mutation (delta F508).
    Kerem E; Corey M; Kerem BS; Rommens J; Markiewicz D; Levison H; Tsui LC; Durie P
    N Engl J Med; 1990 Nov; 323(22):1517-22. PubMed ID: 2233932
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A cystic fibrosis mutation associated with mild lung disease.
    Rusakow LS; Guarín M
    N Engl J Med; 1995 Dec; 333(24):1644. PubMed ID: 7477213
    [No Abstract]   [Full Text] [Related]  

  • 16. When to suspect atypical cystic fibrosis.
    Chawla A; Turcotte FG; Usmani K; Kanu AC
    J Fam Pract; 2010 Sep; 59(9):509-13. PubMed ID: 20824227
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Cystic fibrosis, Young's syndrome, and normal sweat chloride.
    Wellesley D; Schwarz M
    Lancet; 1998 Jul; 352(9121):38. PubMed ID: 9800754
    [No Abstract]   [Full Text] [Related]  

  • 18. Clinical spectrum in homozygotes and compound heterozygotes inheriting cystic fibrosis mutation 3849 + 10kbC > T: significance for geneticists.
    Gilbert F; Li Z; Arzimanoglou II; Bialer M; Denning C; Gorvoy J; Honorof J; Ores C; Quittell L; Arzimanoglou I
    Am J Med Genet; 1995 Sep; 58(4):356-9. PubMed ID: 8533846
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Sweat chloride concentration in cystic fibrosis patients with cystic fibrosis trans-membrane conductance regulator 11234V mutation.
    Al-Mendalawi MD; Abdul-Wahab A; Janahi IA; Abdel-Rahman MO
    Saudi Med J; 2010 Mar; 31(3):339-40; author reply 340. PubMed ID: 20231949
    [No Abstract]   [Full Text] [Related]  

  • 20. Phenotypic characterisation of patients with intermediate sweat chloride values: towards validation of the European diagnostic algorithm for cystic fibrosis.
    Goubau C; Wilschanski M; Skalická V; Lebecque P; Southern KW; Sermet I; Munck A; Derichs N; Middleton PG; Hjelte L; Padoan R; Vasar M; De Boeck K
    Thorax; 2009 Aug; 64(8):683-91. PubMed ID: 19318346
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.