acebutolol and Cystic Fibrosis of Pancreas

acebutolol has been researched along with Cystic Fibrosis of Pancreas in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's1 (14.29)18.2507
2000's0 (0.00)29.6817
2010's5 (71.43)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Derry, D; Kathiresan, B; Waine, D1
Gifford, AH1
Clark, HW; Davies, P; Doull, I; Kotecha, S; Madsen, J; McGreal, EP; McKenzie, Z1
Hoo, ZH; Wildman, MJ1
Anderson, GJ; Bell, SC; Lamont, IL; Masel, P; Reid, DW; Smith, DJ1
JONES, RH1
Panagiotidis, CH; Shuman, HA1

Reviews

1 review(s) available for acebutolol and Cystic Fibrosis of Pancreas

ArticleYear
Tinkering with transporters: periplasmic binding protein-dependent maltose transport in E. coli.
    Journal of bioenergetics and biomembranes, 1993, Volume: 25, Issue:6

    Topics: Amino Acid Sequence; ATP-Binding Cassette Transporters; Bacterial Proteins; Biological Transport; Carrier Proteins; Cystic Fibrosis; Cystic Fibrosis Transmembrane Conductance Regulator; Escherichia coli; Escherichia coli Proteins; Humans; Maltose; Maltose-Binding Proteins; Membrane Proteins; Models, Biological; Models, Structural; Molecular Sequence Data; Monosaccharide Transport Proteins; Periplasmic Binding Proteins; Protein Conformation; Sequence Homology, Amino Acid

1993

Other Studies

6 other study(ies) available for acebutolol and Cystic Fibrosis of Pancreas

ArticleYear
The effect of intravenous antibiotics on anaemia in cystic fibrosis.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2013, Volume: 12, Issue:6

    Topics: Anemia, Iron-Deficiency; Cystic Fibrosis; Ferric Compounds; Humans; Hypersensitivity; Lung Diseases; Maltose

2013
Hemoglobin ≤ 12.9 g/dl predicts risk of antibiotic treatment in cystic fibrosis.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2014, Volume: 13, Issue:1

    Topics: Anemia, Iron-Deficiency; Cystic Fibrosis; Ferric Compounds; Humans; Hypersensitivity; Lung Diseases; Maltose

2014
Functional heterogeneity of pulmonary surfactant protein-D in cystic fibrosis.
    Biochimica et biophysica acta, 2013, Volume: 1832, Issue:12

    Topics: Adolescent; Bacterial Infections; Biomarkers; Blotting, Western; Bronchoalveolar Lavage Fluid; Case-Control Studies; Child; Child, Preschool; Chromatography, Gel; Cohort Studies; Cystic Fibrosis; Enzyme-Linked Immunosorbent Assay; Female; Humans; Infant; Inflammation; Male; Maltose; Protein Multimerization; Pulmonary Surfactant-Associated Protein D; Sepharose; Zymosan

2013
Intravenous iron among cystic fibrosis patients.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2012, Volume: 11, Issue:6

    Topics: Anemia, Iron-Deficiency; Cystic Fibrosis; Ferric Compounds; Humans; Hypersensitivity; Infusions, Intravenous; Iron; Lung Diseases; Maltose; Retrospective Studies

2012
Accurate assessment of systemic iron status in cystic fibrosis will avoid the hazards of inappropriate iron supplementation.
    Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society, 2013, Volume: 12, Issue:3

    Topics: Anemia, Iron-Deficiency; Cystic Fibrosis; Ferric Compounds; Humans; Hypersensitivity; Lung Diseases; Maltose

2013
DISACCHARIDE INTOLERANCE AND MUCOVISCIDOSIS.
    Lancet (London, England), 1964, Jul-18, Volume: 2, Issue:7351

    Topics: Blood Glucose; Carbohydrate Metabolism; Cystic Fibrosis; Diarrhea; Humans; Infant; Lactose; Maltose; Sucrose

1964