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Journal Abstract Search

139 related items for PubMed ID: 7479641

  • 1. [The importance of lung function as a predictor of 2-year mortality in mucoviscidosis].
    Grasemann H, Wiesemann HG, Ratjen F.
    Pneumologie; 1995 Aug; 49(8):466-9. PubMed ID: 7479641
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  • 2. Prediction of mortality in patients with cystic fibrosis.
    Kerem E, Reisman J, Corey M, Canny GJ, Levison H.
    N Engl J Med; 1992 Apr 30; 326(18):1187-91. PubMed ID: 1285737
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  • 3. Obstruction of the respiratory pathways, its evaluation by methods of functional examination of the lungs and development in patients with cystic fibrosis.
    Houstĕk J, Zapletal A, Samánek M, Vávrová V.
    Czech Med; 1979 Apr 30; 2(1-2):1-10. PubMed ID: 527420
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  • 4. Progression of pulmonary hyperinflation and trapped gas associated with genetic and environmental factors in children with cystic fibrosis.
    Kraemer R, Baldwin DN, Ammann RA, Frey U, Gallati S.
    Respir Res; 2006 Nov 30; 7(1):138. PubMed ID: 17137500
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  • 5. Timing and driving components of the breathing strategy in children with cystic fibrosis during exercise.
    Keochkerian D, Chlif M, Delanaud S, Gauthier R, Maingourd Y, Ahmaidi S.
    Pediatr Pulmonol; 2005 Nov 30; 40(5):449-56. PubMed ID: 16163725
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  • 6. Prognosis of patients with cystic fibrosis awaiting heart and lung transplantation.
    Sharples L, Hathaway T, Dennis C, Caine N, Higenbottam T, Wallwork J.
    J Heart Lung Transplant; 1993 Nov 30; 12(4):669-74. PubMed ID: 8369328
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  • 7. Peak oxygen uptake and mortality in children with cystic fibrosis.
    Pianosi P, Leblanc J, Almudevar A.
    Thorax; 2005 Jan 30; 60(1):50-4. PubMed ID: 15618583
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  • 10. Lung function, pulmonary complications, and mortality after allogeneic blood and marrow transplantation in children.
    Kaya Z, Weiner DJ, Yilmaz D, Rowan J, Goyal RK.
    Biol Blood Marrow Transplant; 2009 Jul 30; 15(7):817-26. PubMed ID: 19539213
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  • 11. [Relation between pulmonary ventilation parameters, exercise tolerance and quality of life in patients with chronic obstructive lung disease].
    Chlumský J, Stĕrbová L, Smolíková L, Matous M, Salajka F.
    Vnitr Lek; 2002 Apr 30; 48(4):320-4. PubMed ID: 12061182
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  • 12. Growth in prepubertal children with cystic fibrosis, homozygous for the Delta F508 mutation.
    Keller BM, Aebischer CC, Kraemer R, Schöni MH.
    J Cyst Fibros; 2003 Jun 30; 2(2):76-83. PubMed ID: 15463854
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  • 13. Body mass index as a predictor of survival in adults with cystic fibrosis referred for lung transplantation.
    Snell GI, Bennetts K, Bartolo J, Levvey B, Griffiths A, Williams T, Rabinov M.
    J Heart Lung Transplant; 1998 Nov 30; 17(11):1097-103. PubMed ID: 9855449
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  • 16. 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 Nov 30; 11(4):350-4. PubMed ID: 8580575
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  • 19. Predictors of mortality in adults with cystic fibrosis.
    Courtney JM, Bradley J, Mccaughan J, O'Connor TM, Shortt C, Bredin CP, Bradbury I, Elborn JS.
    Pediatr Pulmonol; 2007 Jun 30; 42(6):525-32. PubMed ID: 17469153
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  • 20. Late effects of bone marrow transplantation on pulmonary function in children.
    Kaplan EB, Wodell RA, Wilmott RW, Leifer B, Lesser ML, August CS.
    Bone Marrow Transplant; 1994 Oct 30; 14(4):613-21. PubMed ID: 7858537
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