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  1. Cystic Fibrosis

    Cystic fibrosis (CF) is an inherited disease affecting multiple systems, which can result in progressive lung disease, pancreatic insufficiency,...
    Ebru Yalçın, Uğur Özçelik in Airway diseases
    Chapter 2023
  2. Cystic Fibrosis Transmembrane Conductance Regulator (CFTR)-Targeted Therapeutics for Cystic Fibrosis

    Treatment of the common life-limiting genetic disease cystic fibrosis (CF) has been transformed by small molecule therapeutics that target the root...
    Diana-Florentina Veselu, Han-I Yeh, ... David N. Sheppard in Ion Channels as Targets in Drug Discovery
    Chapter 2024
  3. Cystic Fibrosis Chronic Rhinosinusitis

    Chronic rhinosinusitis (CRS) is a pervasive and challenging entity to treat in patients with cystic fibrosis (CF). CF CRS develops as a direct...
    Sei Y. Chung, David A. Gudis, Rodney J. Schlosser in Nasal Polyposis and its Management
    Chapter 2024
  4. Cystic Fibrosis

    Cystic fibrosis (CF) is an inherited multisystem disease. Pulmonary failure, liver cirrhosis, and pancreatic insufficiency, including CF-related...
    Jonathan A. Fridell, Molly A. Bozic, ... John A. Powelson in Transplantation of the Pancreas
    Chapter 2023
  5. Macrolides and Cystic Fibrosis

    Macrolide antibiotics attracted interest as a potential therapy in cystic fibrosis (CF) due to remarkable similarities in pathogenic features with...
    Rishi Pabary, Adam Jaffe, Andrew Bush in Macrolides as Immunomodulatory Agents
    Chapter 2024
  6. Cystic Fibrosis-related Diabetes

    Cystic fibrosis (CF) is a genetic disorder that is primarily known to impact the lungs; however, many patients are also diagnosed with diabetes...
    Ryan Richstein, Trisha Menon, Janice Wang in Diabetes Management in Hospitalized Patients
    Chapter 2023
  7. Cystic Fibrosis

    The cystic fibrosis transmembrane regulator protein (CFTR) is a chloride and bicarbonate channel situated at the apical surface of secretory...
    Chapter 2022
  8. Cystic Fibrosis in Adults

    Cystic fibrosis (CF) occurs due to a mutation in a single gene encoding the cystic fibrosis transmembrane conductance regulator protein (CFTR)...
    Berrin Er, Ebru Damadoglu in Airway diseases
    Chapter 2023
  9. Cystic Fibrosis Management in Develo** Countries

    Cystic fibrosis (CF) is a genetic disorder that affects the respiratory and digestive systems, posing unique challenges in develo** countries. This...
    Living reference work entry 2024
  10. Comparative microbiome analysis in cystic fibrosis and non-cystic fibrosis bronchiectasis.

    Background

    Bronchiectasis is a condition characterized by abnormal and irreversible bronchial dilation resulting from lung tissue damage and can be...

    Heryk Motta, Júlia Catarina Vieira Reuwsaat, ... Lívia Kmetzsch in Respiratory Research
    Article Open access 18 May 2024
  11. Bioassays zur Quantifizierung der „cystic fibrosis transmembrane conductance regulator“-Funktion

    Bioassays for the quantification of the cystic fibrosis transmembrane conductance regulator (CFTR) function play a crucial role in the diagnosis,...

    Sophia T. Pallenberg, Burkhard Tümmler in Monatsschrift Kinderheilkunde
    Article 18 April 2024
  12. Future therapies for cystic fibrosis

    We are currently witnessing transformative change for people with cystic fibrosis with the introduction of small molecule, mutation-specific drugs...

    Lucy Allen, Lorna Allen, ... Jane C. Davies in Nature Communications
    Article Open access 08 February 2023
  13. Update on Cystic Fibrosis in Pediatric Patients

    Purpose of Review

    Cystic fibrosis is an inherited, multisystem disease that affects the gastrointestinal system in numerous ways. This article reviews...

    Sarah Shrager Lusman in Current Gastroenterology Reports
    Article 01 September 2023
  14. Understanding CFTR Functionality: A Comprehensive Review of Tests and Modulator Therapy in Cystic Fibrosis

    Cystic fibrosis is a genetic disorder inherited in an autosomal recessive manner. It is caused by a mutation in the Cystic Fibrosis Transmembrane...

    Shorya Thakur, Ankita, ... Gurvinder Singh in Cell Biochemistry and Biophysics
    Article 04 December 2023
  15. Bronchiectasis in Children Unrelated to Cystic Fibrosis

    Bronchiectasis is characterized by abnormal dilation of bronchi seen on high-resolution computed tomography (HRCT) as a result of damage in the...
    Cansu Yilmaz Yegit, Anne B. Chang, Bulent Karadag in Airway diseases
    Chapter 2023
  16. Novel therapeutic approach for the treatment of cystic fibrosis based on freeze-dried tridrug microparticles to treat cystic fibrosis

    Background

    Cystic fibrosis is a severe, autosomal recessive disease that shortens life expectancy. According to studies, approximately 27% of patients...

    Vinayak D. Kabra, Swaroop R. Lahoti in DARU Journal of Pharmaceutical Sciences
    Article 04 May 2023
  17. Microbiome in Cystic Fibrosis

    Cystic fibrosis (CF) is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene leading to the...
    Lindsay J. Caverly, Lucas R. Hoffman, Edith T. Zemanick in The Microbiome in Respiratory Disease
    Chapter 2022
  18. Cystic fibrosis transmembrane conductance regulator (CFTR): beyond cystic fibrosis

    Background

    The cystic fibrosis transmembrane conductance regulator ( CFTR ) gene has been traditionally linked to cystic fibrosis (CF) inheritance in...

    Giuseppe Fabio Parisi, Federico Mòllica, ... Salvatore Leonardi in Egyptian Journal of Medical Human Genetics
    Article Open access 16 May 2022
  19. Depression, anxiety, and hopelessness in a sample of Egyptian children diagnosed with cystic fibrosis

    Background

    Even though current therapeutic approaches have significantly increased the longevity and standard of living for children suffering from...

    Fadia Zyada, Hala Hamdy, ... Somaya H. Shaheen in Middle East Current Psychiatry
    Article Open access 23 February 2024
  20. The prevalence of developmental defects of enamel in people with cystic fibrosis: a systematic review

    Background

    Oral health impacts systemic health, individual well-being, and quality of life. It is important to identify conditions that may exacerbate...

    Fiona O’Leary, Niamh Coffey, ... Barry Plant in BMC Oral Health
    Article Open access 12 April 2024
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