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Cystic Fibrosis Current Events | Cystic Fibrosis News
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Cystic fibrosis testing -- next steps
Three reports describing advances in cystic fibrosis genetic testing appear in the May 2009 issue of The Journal of Molecular Diagnostics. view more (2009-04-28)
Antibiotic Could Offer Promise For Treatment Of Cystic Fibrosis
The antibiotic azithromycin could offer some benefit to people with cystic fibrosis if they do not respond to conventional treatment, suggest authors of a study in this week's issue of THE LANCET. Cystic fibrosis is a severe genetic disorder-the most commonly recessively inherited disorder in white populations. Treatment is limited, and aimed at... view more... (2002-09-25)
Inhaled Antibiotic For Treatment Of Early Lung Infection In Patients With Cystic Fibrosis (p 983)
Inhalation of the antibiotic tobramycin could have an important future role in reducing lung infection of patients with cystic fibrosis, suggest authors of a research letter in this week's issue of THE LANCET. More than 80% of patients with cystic fibrosis are chronically infected by the bacterium Pseudomonas aeruginosa. Infection reduces lung... view more... (2001-09-19)
THE VALUE OF CYSTIC FIBROSIS SCREENING (p 789)
Research published in this week's issue of THE LANCET concludes that screening babies for cystic fibrosis provides the opportunity for more reliable prenatal diagnosis of the disease. The value of screening for the currently incurable disease cystic fibrosis has been the subject of debate over the past few years. Virginie Scotet and colleagues... view more... (2000-08-30)
Breathe deep: Which patients could benefit from inhaled steroids in cystic fibrosis?
A specific variation in the glucocorticoid receptor gene is associated with lung disease progression in cystic fibrosis, research published this week in the online open access journal Respiratory Research reveals. view more (2007-11-29)
Women with cystic fibrosis "too embarrassed" to seek help for incontinence
A study in this week's BMJ finds that over two-thirds of women with the chest disease cystic fibrosis suffer urinary incontinence, yet are reluctant to seek help. Given that incontinence can affect a patient's ability to perform essential daily treatment procedures, addressing this problem should become part of the routine management of cystic... view more... (2001-06-20)
Scientists discover basic defect in cystic fibrosis airway glands
Scientists at Stanford University have determined that the buildup of sticky mucus found in cystic fibrosis is caused by a loss in the epithelial cell's ability to secrete fluid. view more (2006-03-20)
Trial Reveals Safer And Simpler Approach To Treating Children With Cystic Fibrosis
Treating chest infections in young cystic fibrosis patients with an antibiotic once instead of three times daily is as effective and less toxic, conclude the results of a randomised trial published in this week's issue of THE LANCET. view more (2005-02-09)
Protein opens hope of treatment for cystic fibrosis patients
Scientists have finally identified a direct role for the missing protein that leaves cystic fibrosis patients open to attack from lung-damaging bacteria, the main reason most of them die before their 35th birthday, scientists heard today (Thursday 11 September 2008) at the Society for General Microbiology's Autumn meeting being held this week at... view more... (2008-09-11)
Key Found to Kill Cystic Fibrosis Superbug
Researchers from the Schulich School of Medicine & Dentistry at The University of Western Ontario , working with a group from Edinburgh, have discovered a way to kill the cystic fibrosis superbug, Burkholderia cenocepacia. view more (2007-04-25)
Cystic fibrosis treatments may have unseen long-term benefits
Cystic fibrosis medicines that help to break down mucus in the lungs may carry an unexpected long-term benefit, a study suggests. view more (2009-07-17)
Research promising for cystic fibrosis
New U of T research holds promise for developing innovative therapies against cystic fibrosis and may also serve as a model for future therapies against the HIV virus. view more (2008-03-19)
University of Ulster Innovation Aids Cystic Fibrosis Patients Worldwide
A new exercise technique developed by a University of Ulster physiotherapist is helping cystic fibrosis (CF) sufferers worldwide. The new exercise measuring technique, pioneered by Dr Judy Bradley, a lecturer/practitioner in physiotherapy at the University' of Ulster, is to be discussed by Europe's top clinicians and researchers at a conference... view more... (2003-05-23)
Ibuprofen can slow lung disease in children with cystic fibrosis, Canadian study shows
The results of a clinical trial, published in late August in the Journal of Pediatrics, indicates that, when used as part of routine therapy, high-dose ibuprofen is safe, and effective in slowing down lung disease in children with cystic fibrosis (CF). view more (2007-09-05)
Bone marrow cells can become functional gut lining cells
Researchers report the discovery that cells used in bone marrow transplantation can develop into new cells lining the gut, according to a study by Yale School of Medicine in the Proceedings of the National Academy of Sciences. view more (2006-03-03)
Cystic fibrosis patients' self-assessment of health can predict prognosis
Adult Cystic Fibrosis patients can provide important information that helps to predict their prognosis, according to research that asked 223 adult CF patients to assess their own health and well-being. view more (2008-12-29)
Common antibacterial treatment linked to sensorineural hearing loss in cystic fibrosis patients
An otherwise effective treatment for cystic fibrosis places patients at a high risk of sensorineural hearing loss, according to new research published in the July edition of Otolaryngology-Head and Neck Surgery. view more (2009-07-01)
Tracking Cystic Fibrosis with Mice: DFG fellow develops an animal model for the disease
Cystic fibrosis, also known as mucoviscidosis, is one of the most common genetic diseases with a fatal outcome in western Europe. The disease is caused by a defective gene that affects the salt and fluid composition of respiratory tract secretions. As a result, they become highly viscous. The viscous mucous then clumps in the smaller lung... view more... (2004-04-26)
Clues to gene expression in cystic fibrosis will guide research
Genetics tests could help provide cystic fibrosis (CF) patients with targeted treatment in future, pilot study authors suggest. Results from a French clinical trial published today in BMC Medicine show how a small percentage of CF sufferers with a rare genetic stop mutation responded positively to gentamicin treatment. view more (2007-03-29)
New links in the cystic fibrosis chain uncover potential therapeutics
Cystic fibrosis (CF) is an inherited disease caused by mutations in the CFTR gene. Each mutation has number of effects on the cells of the lungs. view more (2007-10-19)
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