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Journal Abstract Search

136 related items for PubMed ID: 3926979

  • 21. [Nutrition, cystic fibrosis and the digestive tract].
    Olveira G, Olveira C.
    Nutr Hosp; 2008 May; 23 Suppl 2():71-86. PubMed ID: 18714414
    [Abstract] [Full Text] [Related]

  • 22. Prognostic factors associated with patient survival during nutritional rehabilitation in malnourished children and adolescents with cystic fibrosis.
    Levy L, Durie P, Pencharz P, Corey M.
    J Pediatr Gastroenterol Nutr; 1986 Jan; 5(1):97-102. PubMed ID: 3080581
    [Abstract] [Full Text] [Related]

  • 23. Effects of nutritional status on exercise performance in advanced cystic fibrosis.
    Marcotte JE, Canny GJ, Grisdale R, Desmond K, Corey M, Zinman R, Levison H, Coates AL.
    Chest; 1986 Sep; 90(3):375-9. PubMed ID: 3743150
    [Abstract] [Full Text] [Related]

  • 24. Pathogenesis of malnutrition in cystic fibrosis, and its treatment.
    Pencharz PB, Durie PR.
    Clin Nutr; 2000 Dec; 19(6):387-94. PubMed ID: 11104588
    [Abstract] [Full Text] [Related]

  • 25. Prospective evaluation of resting energy expenditure, nutritional status, pulmonary function, and genotype in children with cystic fibrosis.
    Zemel BS, Kawchak DA, Cnaan A, Zhao H, Scanlin TF, Stallings VA.
    Pediatr Res; 1996 Oct; 40(4):578-86. PubMed ID: 8888286
    [Abstract] [Full Text] [Related]

  • 26. [Enteral tube feeding in adult patients with cystic fibrosis and respiratory failure].
    Krylova NA, Amelina EL, Krasovsky SA, Karchevskaya NA, Tarabrin EA, Gasanov AM, Ibragimova DF, Golovinsky SV.
    Ter Arkh; 2017 Oct; 89(12):51-55. PubMed ID: 29411760
    [Abstract] [Full Text] [Related]

  • 27. Nutritional growth retardation is associated with defective lung growth in cystic fibrosis: a preventable determinant of progressive pulmonary dysfunction.
    Thomson MA, Quirk P, Swanson CE, Thomas BJ, Holt TL, Francis PJ, Shepherd RW.
    Nutrition; 1995 Oct; 11(4):350-4. PubMed ID: 8580575
    [Abstract] [Full Text] [Related]

  • 28. The effects of nutritional status and hyperinflation on respiratory muscle strength in children and young adults.
    Lands L, Desmond KJ, Demizio D, Pavilanis A, Coates AL.
    Am Rev Respir Dis; 1990 Jun; 141(6):1506-9. PubMed ID: 2350092
    [Abstract] [Full Text] [Related]

  • 29. Body Weight and Body Mass Index in Patients with End-Stage Cystic Fibrosis Stabilize After the Start of Enteral Tube Feeding.
    Hollander FM, de Roos NM, Belle van Meerkerk G, Teding van Berkhout F, Heijerman HGM, van de Graaf EA.
    J Acad Nutr Diet; 2017 Nov; 117(11):1808-1815. PubMed ID: 28919081
    [Abstract] [Full Text] [Related]

  • 30. 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; 137(3):374-80. PubMed ID: 10969263
    [Abstract] [Full Text] [Related]

  • 31. Short-term clinical, nutritional, and functional effects of continuous elemental enteral alimentation in children with cystic fibrosis.
    Bertrand JM, Morin CL, Lasalle R, Patrick J, Coates AL.
    J Pediatr; 1984 Jan; 104(1):41-6. PubMed ID: 6418872
    [Abstract] [Full Text] [Related]

  • 32. [Nutritional intervention in children and adolescents with cystic fibrosis. Relationship with pulmonary function].
    Martínez-Costa C, Escribano A, Núñez Gómez F, García-Maset L, Luján J, Martínez-Rodríguez L.
    Nutr Hosp; 2005 Jan; 20(3):182-8. PubMed ID: 15989064
    [Abstract] [Full Text] [Related]

  • 33. Nutritional status of children with cystic fibrosis measured by total body potassium as a marker of body cell mass: lack of sensitivity of anthropometric measures.
    McNaughton SA, Shepherd RW, Greer RG, Cleghorn GJ, Thomas BJ.
    J Pediatr; 2000 Feb; 136(2):188-94. PubMed ID: 10657824
    [Abstract] [Full Text] [Related]

  • 34. Enteral tube feeding for individuals with cystic fibrosis: Cystic Fibrosis Foundation evidence-informed guidelines.
    Schwarzenberg SJ, Hempstead SE, McDonald CM, Powers SW, Wooldridge J, Blair S, Freedman S, Harrington E, Murphy PJ, Palmer L, Schrader AE, Shiel K, Sullivan J, Wallentine M, Marshall BC, Leonard AR.
    J Cyst Fibros; 2016 Nov; 15(6):724-735. PubMed ID: 27599607
    [Abstract] [Full Text] [Related]

  • 35. Gastrostomy in infants with neonatal pulmonary disease.
    Guimber D, Michaud L, Storme L, Deschildre A, Turck D, Gottrand F.
    J Pediatr Gastroenterol Nutr; 2003 Apr; 36(4):459-63. PubMed ID: 12658035
    [Abstract] [Full Text] [Related]

  • 36. Caloric intake and eating behavior in infants and toddlers with cystic fibrosis.
    Powers SW, Patton SR, Byars KC, Mitchell MJ, Jelalian E, Mulvihill MM, Hovell MF, Stark LJ.
    Pediatrics; 2002 May; 109(5):E75-5. PubMed ID: 11986481
    [Abstract] [Full Text] [Related]

  • 37. Growth status in children with cystic fibrosis based on the National Cystic Fibrosis Patient Registry data: evaluation of various criteria used to identify malnutrition.
    Lai HC, Kosorok MR, Sondel SA, Chen ST, FitzSimmons SC, Green CG, Shen G, Walker S, Farrell PM.
    J Pediatr; 1998 Mar; 132(3 Pt 1):478-85. PubMed ID: 9544905
    [Abstract] [Full Text] [Related]

  • 38. Nutritional rehabilitation increases resting energy expenditure without affecting protein turnover in patients with cystic fibrosis.
    Vaisman N, Clarke R, Pencharz PB.
    J Pediatr Gastroenterol Nutr; 1991 Nov; 13(4):383-90. PubMed ID: 1779312
    [Abstract] [Full Text] [Related]

  • 39. Short-term nutritional supplementation during management of pulmonary exacerbations in cystic fibrosis: a controlled study, including effects of protein turnover.
    Shepherd RW, Holt TL, Cleghorn G, Ward LC, Isles A, Francis P.
    Am J Clin Nutr; 1988 Aug; 48(2):235-9. PubMed ID: 3136639
    [Abstract] [Full Text] [Related]

  • 40. Enteral tube feeding for cystic fibrosis.
    Conway SP, Morton A, Wolfe S.
    Cochrane Database Syst Rev; 2008 Apr 16; (2):CD001198. PubMed ID: 18425869
    [Abstract] [Full Text] [Related]

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