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PUBMED FOR HANDHELDS

Journal Abstract Search


429 related items for PubMed ID: 18367958

  • 1. Validation of a nutrition risk screening tool for children and adolescents with cystic fibrosis ages 2-20 years.
    McDonald CM.
    J Pediatr Gastroenterol Nutr; 2008 Apr; 46(4):438-46. PubMed ID: 18367958
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  • 2. Evaluation of body mass index percentiles for assessment of malnutrition in children with cystic fibrosis.
    Wiedemann B, Paul KD, Stern M, Wagner TO, Hirche TO, German CFQA Group.
    Eur J Clin Nutr; 2007 Jun; 61(6):759-68. PubMed ID: 17213872
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  • 4. The development, validation and reliability of a nutrition screening tool based on the recommendations of the British Association for Parenteral and Enteral Nutrition (BAPEN).
    Weekes CE, Elia M, Emery PW.
    Clin Nutr; 2004 Oct; 23(5):1104-12. PubMed ID: 15380902
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  • 5. 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
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  • 6. Statistical limitations of percent ideal body weight as measure for nutritional failure in patients with cystic fibrosis.
    Hirche TO, Hirche H, Jungblut S, Stern M, Wagner TO, Wiedemann B, German CFQA Group.
    J Cyst Fibros; 2009 Jul; 8(4):238-44. PubMed ID: 19419910
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  • 7. Validation of a Nutrition Screening Tool for Pediatric Patients with Cystic Fibrosis.
    Souza Dos Santos Simon MI, Forte GC, da Silva Pereira J, da Fonseca Andrade Procianoy E, Drehmer M.
    J Acad Nutr Diet; 2016 May; 116(5):813-8. PubMed ID: 27126153
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  • 10. A comparative study of the commonly used nutritional assessment tools for primary health care.
    Asuzu MC.
    East Afr Med J; 1991 Nov; 68(11):913-22. PubMed ID: 1800086
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  • 11. Growth assessment of paediatric patients with CF comparing different auxologic indicators: A multicentre Italian study.
    Lucidi V, Alghisi F, Raia V, Russo B, Valmarana L, Valmarana R, Coruzzo A, Beschi S, Dester S, Rinaldi D, Maglieri M, Guidotti ML, Ravaioli E, Pesola M, De Alessandri A, Padoan R, Grynzich L, Ratclif L, Repetto T, Ambroni M, Provenzano E, Tozzi AE, Colombo C.
    J Pediatr Gastroenterol Nutr; 2009 Sep; 49(3):335-42. PubMed ID: 19543116
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  • 14. Evidence on improved outcomes with early diagnosis of cystic fibrosis through neonatal screening: enough is enough!
    Farrell PM, Lai HJ, Li Z, Kosorok MR, Laxova A, Green CG, Collins J, Hoffman G, Laessig R, Rock MJ, Splaingard ML.
    J Pediatr; 2005 Sep; 147(3 Suppl):S30-6. PubMed ID: 16202779
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  • 16. The development of a MUAC-for-height reference, including a comparison to other nutritional status screening indicators.
    Mei Z, Grummer-Strawn LM, de Onis M, Yip R.
    Bull World Health Organ; 1997 Sep; 75(4):333-41. PubMed ID: 9342892
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  • 17. Nutritional intake and status in children with cystic fibrosis: does age matter?
    White H, Wolfe SP, Foy J, Morton A, Conway SP, Brownlee KB.
    J Pediatr Gastroenterol Nutr; 2007 Jan; 44(1):116-23. PubMed ID: 17204964
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  • 18. Classification of nutritional status in cystic fibrosis.
    Lai HJ.
    Curr Opin Pulm Med; 2006 Nov; 12(6):422-7. PubMed ID: 17053492
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  • 19. An overview of international literature from cystic fibrosis registries 2. Neonatal screening and nutrition/growth.
    Salvatore D, Buzzetti R, Baldo E, Forneris MP, Lucidi V, Manunza D, Marinelli I, Messore B, Neri AS, Raia V, Furnari ML, Mastella G.
    J Cyst Fibros; 2010 Mar; 9(2):75-83. PubMed ID: 19955022
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  • 20. Description of a standardized nutrition classification plan and its relation to nutritional outcomes in children with cystic fibrosis.
    Leonard A, Davis E, Rosenstein BJ, Zeitlin PL, Paranjape SM, Peeler D, Maynard C, Mogayzel PJ.
    J Pediatr Psychol; 2010 Mar; 35(1):6-13. PubMed ID: 19420226
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