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Healio News 07/23/2019 15:15
Ivacaftor may reduce respiratory infections in cystic fibrosis.
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Business Wire 07/22/2019 14:00
Advances in treatments and care led by the CF Foundation have added decades of life and unprecedented hope for the future for people living with CF.
More from Business Wire: 07/19/2019 06:55
Condition : Confirmed Diagnosis of Cystic Fibrosis Intervention : Other: no intervention Sponsors : University Hospital Inselspital, Berne; University Children's Hospital, Zurich; Centre Hospitalier Universitaire Vaudois; Kantonsspital Aarau; University Children's Hospital Basel Recruiting.
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This review traces the development and use of this combination of CFTR modulators, the first licensed drug for treating the homozygous p.Phe508del CF genotype at the intracellular level by correcting the protein defect.
More from International Journal of COPD: 07/17/2019 08:21
According to a newly published report by, “Worldwide Cystic Fibrosis (CF) Therapeutics Market: Information About Key Drivers, Restraints, And Opportunities 2019-2028“. The prime objective of the report is to deliver a Ten-year (2019-2028) market forecast. The latest study focusing on cystic fibrosis (cf) therapeutics market with topmost companies, to determine, define and analyses the sales size, value, market share, market competition landscape, and recent development. It helps to dec…
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FeedNavigator (EU) 07/16/2019 09:11
Scientists created human pancreas on a chip that allowed them to identify the possible cause of a frequent and deadly complication of cystic fibrosis (CF) called CF-Related Diabetes, or CFRD.
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An airway clearance vest stolen from the home of a 14-year-old teen with cystic fibrosis has been recovered by police in Palo Alto, California, but the teen’s health was in decline after missing her ACT treatments.
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HMC provides all latest medications and treatment methods to individuals with cystic fibrosis.
More from Middle East North Africa Financial Network (MENAFN): (UK) 07/11/2019 10:27
The teenager’s health has deteriorated over the past year (Photo: Clare Marvel) This will eventually result in life-threatening complications – the average life span for people with CF is about 37 years.
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European Respiratory Journal 07/11/2019 03:05
Introduction. Pulmonary inflammation and infection are important clinical and prognostic markers of lung disease in cystic fibrosis (CF). However, whether in young children they are transient findings or have cumulative, long-term impacts on respiratory health is largely unknown. We aimed to determine whether their repeated detection has a deleterious effect on structural lung disease. Methods. All patients aged <6 years with annual computed tomography (CT) and bronchoalveolar lavage (BAL) were included. Structural lung disease on CT (%Disease) was determined using the PRAGMA-CF (Perth–Rotterdam Annotated Grid Morphometric Analysis for CF) method. The number of times free neutrophil elastase (NE) and infection were detected in BAL were counte.
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