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  1. ... the pancreas. It may also be caused by cystic fibrosis (CF), a genetic disorder that causes mucus to ... that can cause it, such as pancreatitis and cystic fibrosis. It can also help in diagnosing the cause ...
  2. ... Onset Laboratory Findings Clinical Features / Comments CFTR 3 ( cystic fibrosis ) Childhood/ adolescence Diagnosis requires ≥2 of following findings: ↑ ... multilobular cirrhosis 4 Synthetic dysfunction is usually minimal. Cystic fibrosis liver disease is diagnosed in 10%-15% of ...
  3. ... et al. Optimal tobramycin dosage in patients with cystic fibrosis--evidence for predictability based on previous drug monitoring. ... gentamicin for treating Pseudomonas pneumonia in patients with cystic fibrosis. Pediatr Pulmonol. 1985 Sep-Oct; 1 (5):238– ...
  4. ... Library of Medicine, MedlinePlus -- medlineplus.gov/copd.html Cystic fibrosis: Centers for Disease Control and Prevention -- www.cdc.gov/cystic-fibrosis/about/ Cystic Fibrosis Foundation -- www.cff.org Genetic ...
  5. ... Srivastava A, Carlin J, et al. Delta-F508 cystic fibrosis mutation is not linked to intussusception: implications for ... al. Safety of live-attenuated influenza vaccination in cystic fibrosis. Pediatrics. 2014;134(4):e983–91. doi: 10. ...
  6. ... exercise training improves glycemic control in adult with cystic fibrosis. Med Sci Sports Exerc . 2017;49(2):231– ... OnadyGM, StolfiA. Insulin and oral agents for managing cystic fibrosis-related diabetes. Cochrane Database of Systematic Reviews: John ...
  7. ... data collection View in own window Description The Cystic Fibrosis Foundation (CFF) Patient Registry is a rare-disease ... drive quality improvement in care for patients with cystic fibrosis (CF). Sponsor Cystic Fibrosis Foundation Year Started 1986 ...
  8. ... As medicine, it’s possibly safe when used appropriately. Cystic fibrosis: Cystic fibrosis can lower salt levels in the body. Some people with cystic fibrosis need to take fluids or pills to increase ...
  9. ... 2 4 *Amyotrophic Lateral Sclerosis/ 5 *Bronchiectasis/ 6 *Cystic Fibrosis/ 7 *Hypercapnia/ 8 *Hypoventilation/ 9 *Idiopathic Pulmonary Fibrosis/ ... Obstructive Pulmonary Disease*” or “congenital structual myopath*” or “Cystic Fibrosis” or hypercapnia or hypoventilation or “Interstitial Lung Disease*” ...
  10. ... NP_000177 ​.2 Hoffman et al [2014] CFTR Cystic fibrosis AR c.1521_1523delCTT p.Phe508del 77% 1/ ... NM_000492 ​.4 NP_000483 ​.3 Klinger [1983] , Cystic Fibrosis Genetic Analysis Consortium [1994] c.1364C>A p. ...
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