BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

125 related articles for article (PubMed ID: 6741526)

  • 1. Salivary ribonuclease in cystic fibrosis and control subjects.
    Bardon A; Ceder O; Ekbohm G; Kollberg H
    Acta Paediatr Scand; 1984 Mar; 73(2):263-6. PubMed ID: 6741526
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Properties of purified salivary ribonuclease, and salivary ribonuclease levels in children with cystic fibrosis and in heterozygous carriers.
    Bardoń A; Shugar D
    Clin Chim Acta; 1980 Feb; 101(1):17-24. PubMed ID: 7357736
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Ribonuclease in different types of saliva from cystic fibrosis patients.
    Ceder O; van Dijken J; Ericson T; Kollberg H
    Acta Paediatr Scand; 1985 Jan; 74(1):102-6. PubMed ID: 3984714
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Cystic fibrosis. In vitro and in vivo studies on the biochemical background to the pathogenesis.
    Ceder O
    Acta Paediatr Scand Suppl; 1983; 309():1-47. PubMed ID: 6581681
    [TBL] [Abstract][Full Text] [Related]  

  • 5. [Oral health risks in patients with cystic fibrosis].
    Aps JK; Martens LC
    Rev Belge Med Dent (1984); 2004; 59(2):114-20. PubMed ID: 15693167
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Mutans streptococci, lactobacilli and caries experience in cystic fibrosis homozygotes, heterozygotes and healthy controls.
    Aps JK; Van Maele GO; Claeys G; Martens LC
    Caries Res; 2001; 35(6):407-11. PubMed ID: 11799280
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Cystic fibrosis. Carbohydrate metabolism in CF and in animal models for CF.
    Bardoń A
    Acta Paediatr Scand Suppl; 1987; 332():1-30. PubMed ID: 3474861
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Ribonuclease and its inhibitor in red blood cells in CF.
    Bardoń A; Ceder O; Kollberg H
    Acta Univ Carol Med (Praha); 1990; 36(1-4):73-4. PubMed ID: 2130725
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Cystic fibrosis-like changes in saliva of healthy persons subjected to anaerobic exercise.
    Bardón A; Ceder O; Kollberg H
    Clin Chim Acta; 1983 Oct; 133(3):311-6. PubMed ID: 6627689
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Salivary electrolyte concentrations are associated with cystic fibrosis transmembrane regulator genotypes.
    Aps JK; Delanghe J; Martens LC
    Clin Chem Lab Med; 2002 Apr; 40(4):345-50. PubMed ID: 12059073
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Disturbed myeloperoxidase-dependent activity of neutrophils in cystic fibrosis homozygotes and heterozygotes, and its correction by amiloride.
    Witko-Sarsat V; Allen RC; Paulais M; Nguyen AT; Bessou G; Lenoir G; Descamps-Latscha B
    J Immunol; 1996 Sep; 157(6):2728-35. PubMed ID: 8805680
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Distribution of serum amylase isoenzymes in cystic fibrosis homozygotes and heterozygotes.
    Takács O; Sohár I; László A; Pénzes P; Gyurkovits K
    Acta Paediatr Acad Sci Hung; 1977; 18(1):21-6. PubMed ID: 602748
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Mucoviscidosis: total amylase activity of serum and mixed saliva in homozygous and heterozygous subjects.
    László A; Pénzes P; Gyurkovits K
    Acta Paediatr Acad Sci Hung; 1976; 17(4):293-6. PubMed ID: 1030165
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Reliable diagnosis of the major type of cystic fibrosis with fibroblast cultures. A double blind study.
    Hösli P; Kollberg H; Vogt E
    Acta Paediatr Scand; 1978 Sep; 67(5):617-20. PubMed ID: 358738
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Salivary flow rate and biochemical composition analysis in stimulated whole saliva of children with cystic fibrosis.
    da Silva Modesto KB; de Godói Simões JB; de Souza AF; Damaceno N; Duarte DA; Leite MF; de Almeida ER
    Arch Oral Biol; 2015 Nov; 60(11):1650-4. PubMed ID: 26351748
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Serum pancreatic isoamylases in the diagnosis of cystic fibrosis heterozygotes: A non-valuable test.
    Schiotz PO; Magid E
    Clin Genet; 1977 Jan; 11(1):43-5. PubMed ID: 830448
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Age-related abnormalities of circulating polyamines and diamine oxidase activity in cystic fibrosis heterozygotes and homozygotes.
    Baylin SB; Rosenstein BJ; Marton LJ; Lockwood DH
    Pediatr Res; 1980 Aug; 14(8):921-5. PubMed ID: 6775274
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Serum fatty acid profiles in cystic fibrosis patients and their parents.
    Christophe AB; Warwick WJ; Holman RT
    Lipids; 1994 Aug; 29(8):569-75. PubMed ID: 7990664
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Differences between cystic fibrosis and normal saliva alpha-amylase as a function of age and sex.
    Gillard BK; Markman HC; Feig SA
    Pediatr Res; 1978 Aug; 12(8):868-72. PubMed ID: 308213
    [No Abstract]   [Full Text] [Related]  

  • 20. Detection of cystic fibrosis heterozygotes using the zeta potential reduction method.
    Litt M; Khan MA
    Tex Rep Biol Med; 1976; 34(1):151-4. PubMed ID: 996785
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.