"Cystic Fibrosis" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION.
Descriptor ID |
D003550
|
MeSH Number(s) |
C06.689.202 C08.381.187 C16.320.190 C16.614.213
|
Concept/Terms |
Pancreatic Cystic Fibrosis- Pancreatic Cystic Fibrosis
- Cystic Fibrosis, Pancreatic
- Fibrocystic Disease of Pancreas
- Pancreas Fibrocystic Disease
- Pancreas Fibrocystic Diseases
- Cystic Fibrosis of Pancreas
|
Below are MeSH descriptors whose meaning is more general than "Cystic Fibrosis".
Below are MeSH descriptors whose meaning is more specific than "Cystic Fibrosis".
This graph shows the total number of publications written about "Cystic Fibrosis" by people in this website by year, and whether "Cystic Fibrosis" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
---|
1994 | 2 | 1 | 3 |
1995 | 1 | 0 | 1 |
1996 | 1 | 0 | 1 |
1997 | 3 | 0 | 3 |
1998 | 1 | 0 | 1 |
1999 | 1 | 0 | 1 |
2000 | 1 | 0 | 1 |
2001 | 3 | 0 | 3 |
2002 | 4 | 1 | 5 |
2003 | 1 | 0 | 1 |
2004 | 7 | 1 | 8 |
2005 | 5 | 1 | 6 |
2006 | 3 | 0 | 3 |
2007 | 5 | 2 | 7 |
2008 | 5 | 1 | 6 |
2009 | 13 | 0 | 13 |
2010 | 11 | 1 | 12 |
2011 | 10 | 0 | 10 |
2012 | 7 | 0 | 7 |
2013 | 1 | 1 | 2 |
2014 | 7 | 0 | 7 |
2015 | 13 | 0 | 13 |
2016 | 10 | 1 | 11 |
2017 | 12 | 0 | 12 |
2018 | 13 | 1 | 14 |
2019 | 17 | 2 | 19 |
2020 | 16 | 1 | 17 |
2021 | 18 | 0 | 18 |
2022 | 12 | 0 | 12 |
2023 | 1 | 0 | 1 |
To return to the timeline,
click here.
Below are the most recent publications written about "Cystic Fibrosis" by people in Profiles.
-
Active cycle of breathing technique for cystic fibrosis. Cochrane Database Syst Rev. 2023 02 02; 2:CD007862.
-
Chronic rhinosinusitis in people with Cystic Fibrosis: Expanding evidence and future directions. J Cyst Fibros. 2022 09; 21(5):737-738.
-
Telehealth and CFTR modulators: Accelerating innovative models of cystic fibrosis care. J Cyst Fibros. 2023 Jan; 22(1):9-16.
-
Abdominal Surgical Procedures in Adult Patients With Cystic Fibrosis: What Are the Risks? Dis Colon Rectum. 2022 08 01; 65(8):e805-e815.
-
Clearing the air: Uniquely engaging furin as an approach to cystic fibrosis therapy. Cell Chem Biol. 2022 06 16; 29(6):927-929.
-
Antipseudomonal treatment decisions during CF exacerbation management. J Cyst Fibros. 2022 09; 21(5):753-758.
-
A case report of CFTR modulator administration via carrier mother to treat meconium ileus in a F508del homozygous fetus. J Cyst Fibros. 2022 07; 21(4):721-724.
-
Obesity in Cystic fibrosis: prevalence, trends and associated factors data from the US cystic fibrosis foundation patient registry. J Cyst Fibros. 2022 09; 21(5):777-783.
-
Health care costs in a randomized trial of antimicrobial duration among cystic fibrosis patients with pulmonary exacerbations. J Cyst Fibros. 2022 07; 21(4):594-599.
-
Rapid expansion and extinction of antibiotic resistance mutations during treatment of acute bacterial respiratory infections. Nat Commun. 2022 03 09; 13(1):1231.