Pulmonary Fibrosis Current Events | Pulmonary Fibrosis News | 2
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Shorter distance on six-minute walk test points up a greater risk of death
For idiopathic pulmonary fibrosis (IPF) patients awaiting lung transplantation, a simple walk test can predict mortality rates. view more (2006-09-18)
p90RSK: A new therapeutic target for liver fibrosis?
Cirrhosis is a world wide, bad prognosis liver disease and characterized by excessive collagen deposition and liver function damage. view more (2009-05-13)
Liver fibrosis will be treated by a potential target
The outcome of hepatitis is either self recovery or its development into liver fibrosis or, further, liver cirrhosis. Liver fibrosis is the early pathological process of cirrhosis, which is considered a reversible, wound-healing response. Since no ideal drug is available for its therapy, liver fibrosis is currently considered to be a major... view more... (2007-10-17)
Heart catheters do not benefit patients
Doctors should probably stop using pulmonary artery catheters because they do not benefit patients, say doctors from Australia in this week's BMJ. view more (2006-11-03)
An effective strategy for inhibition of cirrhosis
In China, the incidence of liver cirrhosis is still high, although new therapeutic approaches have recently been proposed, there is no established therapy for liver fibrosis, and Authors investigated the prevention effects of Chinese Medicine Qianggan-Rongxian Soup on liver fibrosis induced by DMN in rat. view more (2008-09-25)
Pulmonary CT angiography identifies disease and injury beyond the pulmonary arteries in children
Computed tomography angiography (CTA) can identify abnormalities and injury beyond the pulmonary arteries, including broken bones and heart disease, according to a study published in the September issue of the American Journal of Roentgenology (AJR) view more (2009-08-19)
Breath test offers hope for early detection of lung-bacteria growth in cystic fibrosis
Breath-analysis testing may prove to be an effective, non-invasive method for detecting the damaging lung-bacteria growth seen in cystic fibrosis, which would allow for early stage treatments that can extend the health of people with this disease. view more (2005-10-18)
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)
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)
U-M scientists target key cells and signals that trigger pulmonary fibrosis
Scientists at the University of Michigan Medical School have identified biochemical signals that attract pathogenic cells to damaged lung tissue - one of the first steps in a chain of events leading to a lethal disease called idiopathic pulmonary fibrosis or IPF. view more (2006-05-24)
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)
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)
UCSF marks a milestone with 500th transplant in heart and lung program
UCSF marked a milestone this week with the 500th procedure in its Thoracic Transplant Program, which specializes in transplantation of the heart and lung. view more (2008-04-25)
Double threat: Deadly lung disease also linked to heart attacks
Patients with idiopathic pulmonary fibrosis (IPF) are three times as likely to experience severe coronary events-including heart attacks-than people without the disease. view more (2008-12-05)
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)
Study reveals how cells destroy faulty proteins in cystic fibrosis
The cellular system that degrades faulty proteins created by the cystic fibrosis gene has been identified by University of North Carolina at Chapel Hill scientists. view more (2006-08-11)
Note to people with scarred and stiffened lungs: Monitor your sleep before severe fatigue sets in
Family, friends and neighbors remember Lisa Sandler Spaeth as an active mother of two in Potomac, Md., with a lot on the go, juggling her son's baseball games and her daughter's horseback-riding lessons with numerous committee obligations, organizing women's activities at her local synagogue. view more (2008-07-30)
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