Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

[Cystic fibrosis]

F J Reis1, N Damaceno

  • 1Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, MG, Brazil.

Jornal De Pediatria
|December 20, 2003
PubMed
Summary
This summary is machine-generated.

This review synthesizes recent advances in Cystic Fibrosis (CF) treatment and understanding. It provides pediatricians with essential knowledge on CF genetics, diagnosis, and management.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

[Study of intestinal malabsorption diseases as cause of monosymptomatic short stature]

Jornal de pediatria·2003
Same author

Prognostic aspects of cystic fibrosis in Brazil.

Annals of tropical paediatrics·2001
Same author

[Clinical and nutritional aspects in patients with cystic fibrosis: 20 years of follow-up in the Clinical Hospital-Federal University of Minas Gerais (HC-UFMG)].

Revista da Associacao Medica Brasileira (1992)·2001
Same author

Molecular analysis in Brazilian cystic fibrosis patients reveals five novel mutations.

Genetic testing·2000
Same author

Evolution of IgA deficiency to IgG subclass deficiency and common variable immunodeficiency.

Allergologia et immunopathologia·2000
Same author

Survival analysis for cystic fibrosis in Minas Gerais State, Brazil.

Journal of tropical pediatrics·1999

Area of Science:

  • Pulmonology
  • Genetics
  • Pediatrics

Background:

  • Recent significant advancements in Cystic Fibrosis (CF) treatment necessitate updated clinical knowledge.
  • Pediatricians require a comprehensive understanding of CF for effective patient care.

Purpose of the Study:

  • To conduct an extensive review of the latest international literature on Cystic Fibrosis.
  • To provide a practical and up-to-date synthesis of CF for healthcare professionals.

Main Methods:

  • Systematic selection of prominent recent publications on Cystic Fibrosis from international sources.
  • Compilation and synthesis of information to create a comprehensive overview.

Main Results:

  • Detailed review covering historical aspects, genetics, and physiopathology of CF.

Related Experiment Videos

  • In-depth analysis of pulmonary infection microbiology, clinical manifestations, and diagnostic criteria (clinical and laboratory).
  • Exploration of differential diagnosis, current treatment strategies, and patient prognosis in Cystic Fibrosis.
  • Conclusions:

    • This review offers a consolidated resource on Cystic Fibrosis, integrating recent therapeutic progress.
    • It aims to enhance pediatricians' understanding and management of Cystic Fibrosis patients.