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 *

246 related articles for article (PubMed ID: 11966405)

  • 1. Towards the pharmacogenomics of cystic fibrosis.
    Sangiuolo F; D'Apice MR; Bruscia E; Lucidi V; Novelli G
    Pharmacogenomics; 2002 Jan; 3(1):75-87. PubMed ID: 11966405
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype-phenotype correlation in cystic fibrosis patients.
    Ferrari M; Cremonesi L
    Ann Biol Clin (Paris); 1996; 54(6):235-41. PubMed ID: 8949420
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Cystic fibrosis transmembrane conductance regulator (CFTR) gene: mutations and clinical phenotypes].
    Schwartz M
    Ugeskr Laeger; 2003 Feb; 165(9):912-6. PubMed ID: 12661515
    [TBL] [Abstract][Full Text] [Related]  

  • 4. [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; 129 Suppl 1():6-9. PubMed ID: 15637983
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Genotype-phenotype correlation in a sample of Mexican patients with cystic fibrosis].
    Yokoyama E; Lezana JL; Vigueras-Villaseñor RM; Rojas-Castañeda J; Saldaña-Álvarez Y; Orozco L; Chávez-Saldaña M
    Rev Invest Clin; 2013; 65(6):491-9. PubMed ID: 24687356
    [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. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K; Weren M; Proesmans M; Kerem E
    Pediatrics; 2005 Apr; 115(4):e463-9. PubMed ID: 15772171
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.
    Thauvin-Robinet C; Munck A; Huet F; de Becdelièvre A; Jimenez C; Lalau G; Gautier E; Rollet J; Flori J; Nové-Josserand R; Soufir JC; Haloun A; Hubert D; Houssin E; Bellis G; Rault G; David A; Janny L; Chiron R; Rives N; Hairion D; Collignon P; Valeri A; Karsenty G; Rossi A; Audrézet MP; Férec C; Leclerc J; Georges Md; Claustres M; Bienvenu T; Gérard B; Boisseau P; Cabet-Bey F; Cheillan D; Feldmann D; Clavel C; Bieth E; Iron A; Simon-Bouy B; Izard V; Steffann J; Viville S; Costa C; Drouineaud V; Fauque P; Binquet C; Bonithon-Kopp C; Morris MA; Faivre L; Goossens M; Roussey M; Girodon E;
    J Med Genet; 2013 Apr; 50(4):220-7. PubMed ID: 23378603
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Recommendations for the classification of diseases as CFTR-related disorders.
    Bombieri C; Claustres M; De Boeck K; Derichs N; Dodge J; Girodon E; Sermet I; Schwarz M; Tzetis M; Wilschanski M; Bareil C; Bilton D; Castellani C; Cuppens H; Cutting GR; Drevínek P; Farrell P; Elborn JS; Jarvi K; Kerem B; Kerem E; Knowles M; Macek M; Munck A; Radojkovic D; Seia M; Sheppard DN; Southern KW; Stuhrmann M; Tullis E; Zielenski J; Pignatti PF; Ferec C
    J Cyst Fibros; 2011 Jun; 10 Suppl 2():S86-102. PubMed ID: 21658649
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Molecular basis of phenotype heterogeneity in cystic fibrosis].
    Bienvenu T
    Ann Biol Clin (Paris); 1997; 55(2):113-21. PubMed ID: 9180964
    [TBL] [Abstract][Full Text] [Related]  

  • 12. [Epidemiologic study of the cystic fibrosis gene in the Champagne-Ardenne region].
    Clavel C; Pennaforte F; Pigeon F; Mozelle M; Boutterin MC; Duval-Binninger I; F-erec C; Birembaut P
    Ann Biol Clin (Paris); 1996; 54(2):67-74. PubMed ID: 8763629
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Intestinal current measurement for diagnostic classification of patients with questionable cystic fibrosis: validation and reference data.
    Derichs N; Sanz J; Von Kanel T; Stolpe C; Zapf A; Tümmler B; Gallati S; Ballmann M
    Thorax; 2010 Jul; 65(7):594-9. PubMed ID: 20627915
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Non-classic cystic fibrosis associated with D1152H CFTR mutation.
    Burgel PR; Fajac I; Hubert D; Grenet D; Stremler N; Roussey M; Siret D; Languepin J; Mely L; Fanton A; Labbé A; Domblides P; Vic P; Dagorne M; Reynaud-Gaubert M; Counil F; Varaigne F; Bienvenu T; Bellis G; Dusser D
    Clin Genet; 2010 Apr; 77(4):355-64. PubMed ID: 19843100
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
    Sermet-Gaudelus I; Girodon E; Sands D; Stremmler N; Vavrova V; Deneuville E; Reix P; Bui S; Huet F; Lebourgeois M; Munck A; Iron A; Skalicka V; Bienvenu T; Roussel D; Lenoir G; Bellon G; Sarles J; Macek M; Roussey M; Fajac I; Edelman A
    Am J Respir Crit Care Med; 2010 Oct; 182(7):929-36. PubMed ID: 20538955
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [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
    [TBL] [Abstract][Full Text] [Related]  

  • 17. [Cystic fibrosis: molecular update and clinical implications].
    Orozco L; Chávez M; Saldaña Y; Velázquez R; Carnevale A; González-del Angel A; Jiménez S
    Rev Invest Clin; 2006; 58(2):139-52. PubMed ID: 16827266
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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; 20(3):164-8. PubMed ID: 18301294
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
    Claustres M; Guittard C; Bozon D; Chevalier F; Verlingue C; Ferec C; Girodon E; Cazeneuve C; Bienvenu T; Lalau G; Dumur V; Feldmann D; Bieth E; Blayau M; Clavel C; Creveaux I; Malinge MC; Monnier N; Malzac P; Mittre H; Chomel JC; Bonnefont JP; Iron A; Chery M; Georges MD
    Hum Mutat; 2000; 16(2):143-56. PubMed ID: 10923036
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 13.