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Journal Abstract Search

370 related items for PubMed ID: 24757043

  • 1. Overweight and obesity in patients with cystic fibrosis: a center-based analysis.
    Hanna RM, Weiner DJ.
    Pediatr Pulmonol; 2015 Jan; 50(1):35-41. PubMed ID: 24757043
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  • 7. Nutritional status and lung function in children with pancreatic-sufficient cystic fibrosis.
    Madde A, Okoniewski W, Sanders DB, Ren CL, Weiner DJ, Forno E.
    J Cyst Fibros; 2022 Sep; 21(5):769-776. PubMed ID: 34972650
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  • 8. Dietary intake, weight status, pulmonary function, and metabolic profile in children with cystic fibrosis with or without pancreatic sufficiency.
    Papachristou E, Katsagoni CN, Roussou X, Tokou I, Moustaki M, Petrocheilou A, Yannakoulia M, Loukou I.
    Nutrition; 2023 Oct; 114():112091. PubMed ID: 37356169
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  • 9. Cystic-fibrosis related-diabetes (CFRD) is preceded by and associated with growth failure and deteriorating lung function.
    Terliesner N, Vogel M, Steighardt A, Gausche R, Henn C, Hentschel J, Kapellen T, Klamt S, Gebhardt J, Kiess W, Prenzel F.
    J Pediatr Endocrinol Metab; 2017 Aug 28; 30(8):815-821. PubMed ID: 28245190
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  • 10. Longitudinal relationship among growth, nutritional status, and pulmonary function in children with cystic fibrosis: analysis of the Cystic Fibrosis Foundation National CF Patient Registry.
    Zemel BS, Jawad AF, FitzSimmons S, Stallings VA.
    J Pediatr; 2000 Sep 28; 137(3):374-80. PubMed ID: 10969263
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  • 11. Association of the relative change in weight and body mass index with lung function in teenagers and adults with cystic fibrosis: Influence of gender and diabetes.
    Cano Megías M, Guisado Vasco P, González Albarrán O, Lamas Ferreiro A, Máiz Carro L.
    Endocrinol Nutr; 2015 Nov 28; 62(9):422-9. PubMed ID: 26311609
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  • 12. Nutritional status in the era of highly effective CFTR modulators.
    Bass R, Alvarez JA.
    Pediatr Pulmonol; 2024 Sep 28; 59 Suppl 1():S6-S16. PubMed ID: 39105341
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  • 14. Obesity in Cystic fibrosis: prevalence, trends and associated factors data from the US cystic fibrosis foundation patient registry.
    Szentpetery S, Fernandez GS, Schechter MS, Jain R, Flume PA, Fink AK.
    J Cyst Fibros; 2022 Sep 28; 21(5):777-783. PubMed ID: 35396178
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  • 15. Pancreatitis among patients with cystic fibrosis: correlation with pancreatic status and genotype.
    De Boeck K, Weren M, Proesmans M, Kerem E.
    Pediatrics; 2005 Apr 28; 115(4):e463-9. PubMed ID: 15772171
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  • 16. Factors associated with FEV1 decline in cystic fibrosis: analysis of the ECFS patient registry.
    Kerem E, Viviani L, Zolin A, MacNeill S, Hatziagorou E, Ellemunter H, Drevinek P, Gulmans V, Krivec U, Olesen H, ECFS Patient Registry Steering Group.
    Eur Respir J; 2014 Jan 28; 43(1):125-33. PubMed ID: 23598952
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  • 17. 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 28; 13(4):478-84. PubMed ID: 24359972
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  • 18. Cystic fibrosis related diabetes in Europe: Prevalence, risk factors and outcome; Olesen et al.
    Olesen HV, Drevinek P, Gulmans VA, Hatziagorou E, Jung A, Mei-Zahav M, Stojnic N, Thomas M, Zolin A, ECFSPR Steering Group.
    J Cyst Fibros; 2020 Mar 28; 19(2):321-327. PubMed ID: 31680042
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  • 19. Nutritional Status in Childhood as a Prognostic Factor in Patients with Cystic Fibrosis.
    Ashkenazi M, Nathan N, Sarouk I, Aluma BEB, Dagan A, Bezalel Y, Keler S, Vilozni D, Efrati O.
    Lung; 2019 Jun 28; 197(3):371-376. PubMed ID: 30887107
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  • 20. Glucose intolerance in children with cystic fibrosis.
    Solomon MP, Wilson DC, Corey M, Kalnins D, Zielenski J, Tsui LC, Pencharz P, Durie P, Sweezey NB.
    J Pediatr; 2003 Feb 28; 142(2):128-32. PubMed ID: 12584532
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