"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 |
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1994 | 3 | 0 | 3 |
1995 | 1 | 1 | 2 |
1996 | 4 | 0 | 4 |
1997 | 3 | 1 | 4 |
1998 | 3 | 2 | 5 |
1999 | 7 | 1 | 8 |
2000 | 3 | 1 | 4 |
2001 | 1 | 1 | 2 |
2002 | 4 | 1 | 5 |
2003 | 4 | 3 | 7 |
2004 | 4 | 0 | 4 |
2005 | 3 | 1 | 4 |
2006 | 3 | 2 | 5 |
2007 | 4 | 3 | 7 |
2008 | 3 | 4 | 7 |
2009 | 2 | 0 | 2 |
2010 | 6 | 1 | 7 |
2011 | 7 | 0 | 7 |
2012 | 7 | 1 | 8 |
2013 | 6 | 0 | 6 |
2014 | 6 | 3 | 9 |
2015 | 5 | 0 | 5 |
2016 | 2 | 0 | 2 |
2017 | 7 | 3 | 10 |
2018 | 4 | 1 | 5 |
2019 | 7 | 4 | 11 |
2020 | 9 | 1 | 10 |
2021 | 10 | 0 | 10 |
2022 | 10 | 0 | 10 |
2023 | 11 | 0 | 11 |
2024 | 4 | 0 | 4 |
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Below are the most recent publications written about "Cystic Fibrosis" by people in Profiles.
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Cystic fibrosis-related diabetes screening at a large pediatric center. Lab Med. 2024 Sep 04; 55(5):580-584.
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Advanced cystic fibrosis liver disease: Endovascular, endoscopic, radiologic, and surgical considerations. Pediatr Pulmonol. 2024 Sep; 59 Suppl 1:S115-S122.
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Cystic Fibrosis Foundation Evidence-Based Guideline for the Management of CRMS/CFSPID. Pediatrics. 2024 May 01; 153(5).
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Optimizing sexual reproductive health of men and women with cystic fibrosis: A systematic review. J Cyst Fibros. 2024 Jul; 23(4):633-638.
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Interlaboratory comparison of Pseudomonas aeruginosa phage susceptibility testing. J Clin Microbiol. 2023 12 19; 61(12):e0061423.
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Inflammatory Activity of Epithelial Stem Cell Variants from Cystic Fibrosis Lungs Is Not Resolved by CFTR Modulators. Am J Respir Crit Care Med. 2023 11 01; 208(9):930-943.
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Prospective study of quantitative liver MRI in cystic fibrosis: feasibility and comparison to PUSH cohort ultrasound. Pediatr Radiol. 2023 10; 53(11):2210-2220.
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Role of hyperglycemia in cystic fibrosis pulmonary exacerbations. J Cyst Fibros. 2023 09; 22(5):868-874.
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Massive and Lengthy Clonal Nosocomial Expansion of Mycobacterium abscessus subsp. massiliense among Patients Who Are Ventilator Dependent without Cystic Fibrosis. Microbiol Spectr. 2023 08 17; 11(4):e0490822.
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Treatment of Fetal Cystic Fibrosis With Cystic Fibrosis Transmembrane Conductance Regulator Modulation Therapy. Ann Intern Med. 2023 07; 176(7):1015-1016.