TITLE

Cystic fibrosis. 2. Lung injury in cystic fibrosis

AUTHOR(S)
Elborn, J S; Shale, D J
PUB. DATE
December 1990
SOURCE
Thorax;Dec1990, Vol. 45 Issue 12, p970
SOURCE TYPE
Academic Journal
DOC. TYPE
Article
ABSTRACT
No abstract available.
ACCESSION #
66101487

 

Related Articles

  • Ireland has the highest rate of cystic fibrosis in the world.  // Daily Mail;1/22/2016, p22 

    WHAT IS CYSTIC FIBROSIS?

  • Two biotech IPOs make debut. Investor's Business Daily // Investors Business Daily;9/19/2014, pA02 

    Cystic fibrosis therapy developer

  • CF: Not just a pediatric problem anymore. George, Maureen Redmond; Mauro, Elizabeth // RN;Sep90, Vol. 53 Issue 9, p60 

    Discusses the care and support available for adults with cystic fibrosis. Average age of survival for cystic fibrosis patients; Complications of cystic fibrosis; Treatment for cystic fibrosis.

  • Cystic Fibrosis. Coates, Allan L. // New England Journal of Medicine;8/24/95, Vol. 333 Issue 8, p534 

    This article reviews the book "Cystic Fibrosis."

  • Cystic Fibrosis.  // Current Medical Literature: Respiratory Medicine;2007, Vol. 21 Issue 1, p8 

    The article presents abstracts of medical research related to cystic fibrosis. They include "Pneumothorax in cystic fibrosis: A retrospective case series," "Classifying severity of cystic fibrosis lung disease using longitudinal pulmonary function data" and "Effect of allergic bronchopulmonary...

  • The neglected ion: HCO3-. Quinton, Paul M. // Nature Medicine;Mar2001, Vol. 7 Issue 3, p292 

    Focuses on the function of the cystic fibrosis transmembrane conductance regulator. Role of cystic fibrosis transport; Characteristics of cystic fibrosis.

  • THE CULTURE OF PRIMARY BRONCHIAL EPITHELIAL CELLS FROM THE LUNGS OF PEOPLE WITH CYSTIC FIBROSIS REMOVED AT THE TIME OF TRANSPLANTATION: A MODEL TO STUDY CYSTIC FIBROSIS LUNG DISEASE.  // Thorax;Dec2008 Supplement 7, Vol. 63, pA38 

    An abstract of the article "The Culture of Primary Bronchial Epithelial Cells From the Lungs of People With Cystic Fibrosis Removed at the Time of Transplantation: A Model to Study Cystic Fibrosis Lung Disease," by M. Brodlie and colleagues is presented.

  • CFTR Molecular Analysis Reveals Infrequent Allele Frequencies in Nine Cystic Fibrosis Patients from São Paulo State, Brazil. Goloni-Bertollo, Eny Maria; Rossit, Andréa Regina B.; Batista, Jaõo; Junior, Salomão; Fett-Conte, Agnes Cristina; Raskin, Salmo // Human Biology;Jun2003, Vol. 75 Issue 3, p393 

    Studies the CFTR gene mutation in patients with cystic fibrosis in Sao Paulo, Brazil. Frequencies of cystic fibrosis mutations; Molecular and clinical characteristics of patients with cystic fibrosis.

  • Recent advances in cystic fibrosis. Doull, Iolo J. M. // Archives of Disease in Childhood;Jul2001, Vol. 85 Issue 1, p62 

    The median life expectancy for cystic fibrosis is now over 30 years, and it is projected that in newborn infants it will become more than 40 years. The identification of the cystic fibrosis gene and its product, cystic fibrosis transmembrane conductance regulator (CFTR), has widened the spectrum...

  • When that dying patient calls you Mommy. Perilman, Toby N. // RN;Aug86, Vol. 49 Issue 8, p24 

    Presents an article on how a nurse care for a child with a chronic cystic fibrosis. Changes in the appearance of a patient with cystic fibrosis; Facts about cystic fibrosis. INSETS: Some facts about cystic fibrosis;How CF is inherited.

Share

Read the Article

Courtesy of VIRGINIA BEACH PUBLIC LIBRARY AND SYSTEM

Sign out of this library

Other Topics