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PUBMED FOR HANDHELDS

Journal Abstract Search


496 related items for PubMed ID: 30913015

  • 21. Insulin resistance, β-cell dysfunction and differences in curves of plasma glucose and insulin in the intermediate points of the standard glucose tolerance test in adults with cystic fibrosis.
    Cano Megías M, González Albarrán O, Guisado Vasco P, Lamas Ferreiro A, Máiz Carro L.
    Endocrinol Nutr; 2015 Feb; 62(2):91-9. PubMed ID: 25444978
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  • 22. Predictors for future cystic fibrosis-related diabetes by oral glucose tolerance test.
    Schmid K, Fink K, Holl RW, Hebestreit H, Ballmann M.
    J Cyst Fibros; 2014 Jan; 13(1):80-5. PubMed ID: 23809507
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  • 24. Abnormal glucose tolerance and lung function in children with cystic fibrosis. Comparing oral glucose tolerance test and continuous glucose monitoring.
    Elidottir H, Diemer S, Eklund E, Hansen CR.
    J Cyst Fibros; 2021 Sep; 20(5):779-784. PubMed ID: 33478894
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  • 28. β-Cell secretory defects are present in pancreatic insufficient cystic fibrosis with 1-hour oral glucose tolerance test glucose ≥155 mg/dL.
    Nyirjesy SC, Sheikh S, Hadjiliadis D, De Leon DD, Peleckis AJ, Eiel JN, Kubrak C, Stefanovski D, Rubenstein RC, Rickels MR, Kelly A.
    Pediatr Diabetes; 2018 Nov; 19(7):1173-1182. PubMed ID: 29885044
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  • 29. Peak OGTT glucose is associated with lower lung function in young children with cystic fibrosis.
    Prentice BJ, Chelliah A, Ooi CY, Hameed S, Verge CF, Plush L, Widger J.
    J Cyst Fibros; 2020 Mar; 19(2):305-309. PubMed ID: 31126898
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  • 31. Insulin sensitivity, disposition index and insulin clearance in cystic fibrosis: a cross-sectional study.
    Nielsen BU, Mathiesen IHM, Krogh-Madsen R, Katzenstein TL, Pressler T, Shaw JAM, Rickels MR, Almdal TP, Faurholt-Jepsen D, Stefanovski D.
    Diabetologia; 2024 Oct; 67(10):2188-2198. PubMed ID: 39093413
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  • 32. Early assessment of glucose abnormalities during continuous glucose monitoring associated with lung function impairment in cystic fibrosis patients.
    Leclercq A, Gauthier B, Rosner V, Weiss L, Moreau F, Constantinescu AA, Kessler R, Kessler L.
    J Cyst Fibros; 2014 Jul; 13(4):478-84. PubMed ID: 24359972
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  • 34. Insulin secretion improves in cystic fibrosis following ivacaftor correction of CFTR: a small pilot study.
    Bellin MD, Laguna T, Leschyshyn J, Regelmann W, Dunitz J, Billings J, Moran A.
    Pediatr Diabetes; 2013 Sep; 14(6):417-21. PubMed ID: 23952705
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  • 36. Can continuous glucose monitoring predict cystic fibrosis-related diabetes and worse clinical outcome?
    Zorron M, Marson FAL, Morcillo AM, Gonçalves AC, El Beck MS, Ribeiro JD, Ribeiro AF.
    J Bras Pneumol; 2022 Sep; 48(2):e20210307. PubMed ID: 35475864
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  • 38. Prevalence of Post-Glucose Challenge Hypoglycemia in Adult Patients With Cystic Fibrosis and Relevance to the Risk of Cystic Fibrosis-Related Diabetes.
    Bonhoure A, Potter KJ, Reynaud Q, Boudreau V, Senior PA, Tremblay F, Lavoie A, Durieu I, Rabasa-Lhoret R.
    Can J Diabetes; 2022 Apr; 46(3):294-301.e2. PubMed ID: 35568431
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  • 39. Sensitivity and specificity of different methods for cystic fibrosis-related diabetes screening: is the oral glucose tolerance test still the standard?
    Mainguy C, Bellon G, Delaup V, Ginoux T, Kassai-Koupai B, Mazur S, Rabilloud M, Remontet L, Reix P.
    J Pediatr Endocrinol Metab; 2017 Jan 01; 30(1):27-35. PubMed ID: 27977404
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