Cystic Fibrosis - Causes, Symptoms, Treatment, Diagnosis - Medbroadcast
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Cystic Fibrosis - Causes, Symptoms, Treatment, Diagnosis - Medbroadcast
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Tags: Genetic, Reproductive System, Lung, Cystic Fibrosis, Disease and Condition, Childbirth
Most Recently Shared on June 24, 2010 at 1:28 pm By:
What is cystic fibrosis? http://bit.ly/aStucA + http://bit.ly/c0TBdZ
An Update on the Screening, Diagnosis, Management, and Treatment of Vitamin D Deficiency in Individuals with Cystic Fibrosis: Evidence-Based Recommendations from the Cystic Fibrosis Foundation
jcem.endojournals.org — “An Update on the Screening, Diagnosis, Management, and Treatment of Vitamin D Deficiency in Individuals with Cystic Fibrosis: Evidence-Based Recommendations from the Cystic Fibrosis Foundation” View full resource at jcem.endojournals.org
Most Recently Shared on March 7, 2012 at 2:16 pm By:
Vitamin D guidelines for cystic fibrosis co-sponsored by @CFCanada @CF_Foundation @TheEndoSociety & Peds Endo Society http://t.co/ksINnZeY
JAMA News Releases - November 16, 2010
pubs.ama-assn.org — “Effective Diagnosis, Treatment of Ear Infections in Children Examined in Study;Common Strain of Bacteria Found in Patients With Cystic Fibrosis in Canada; Associated With Greater Risk of Death;Combination Therapy Improves Survival Time For Patients With Advanced Liver Cancer” View full resource at pubs.ama-assn.org
Most Recently Shared on January 13, 2011 at 3:53 pm By:
8/10 kids get better w/o antibx--If treated w amox, an additional 12 might improve, but 10 kids get rash or diarrhea. http://bit.ly/gzRlNQ
Cystic Fibrosis Patients Living Longer - ABC News
abcnews.go.com — “Many with cystic fibrosis are reaching adulthood, and experts attribute the longer life expectancy to earlier diagnosis and improved treatments.” View full resource at abcnews.go.com
Most Recently Shared on June 25, 2010 at 4:03 pm By:
Many With Cystic Fibrosis Living Longer: Many with cystic fibrosis are reaching adulthood, and experts attribute t... http://bit.ly/dnnefu
U.S. Food And Drug Administration Approves Cayston(R) For The Improvement Of Respiratory Symptoms In Cystic Fibrosis Patients
medicalnewstoday.com — “Gilead Sciences, Inc. (Nasdaq:GILD) announced that the U.S. Food and Drug Administration (FDA) has granted marketing approval for Cayston(R)(aztreonam for inhalation solution) as a treatment to im” View full resource at medicalnewstoday.com
Most Recently Shared on February 27, 2010 at 1:37 pm By:
U.S. Food And Drug Administration Approves Cayston(R) For The Improvement Of Respiratory Symptoms In Cystic Fibrosis .. http://bit.ly/9BMpuh
PARI Pharma's Altera Delivers Gilead's Cayston, Approved By The U.S. FDA For The Improvement Of Respiratory Symptoms In Cystic Fibrosis Patients
medicalnewstoday.com — “Altera, which uses eFlow Technology, was cleared to market by the FDA as the first drug-specific nebulizer for use in the treatment of patients with cystic fibrosis and has been specifically devel” View full resource at medicalnewstoday.com
Most Recently Shared on February 24, 2010 at 7:09 pm By:
PARI Pharma's Altera Delivers Gilead's Cayston, Approved By The U.S. FDA For The Improvement Of Respiratory Symptoms I... http://mnt.to/3y3W
Gene Variant Heightens Risk of Severe Liver Disease in Cystic Fibrosis
newswise.com — “A UNC study, which appears in the Sept. 9 issue of the Journal of the American Medical Association (JAMA), could lead to earlier detection and diagnosis of cystic fibrosis liver disease and better treatment options for the patients affected by the disease.” View full resource at newswise.com
Most Recently Shared on September 8, 2009 at 9:19 pm By:
Gene variant heightens risk of severe liver disease in cystic fibrosis http://bit.ly/2pwWM
Intervention in infants with cystic fibrosis key to slowing progression
eurekalert.org — “Early detection of lung disease in cystic fibrosis (CF), combined with aggressive treatment in infants, may be the key to controlling the progression of the disease, according to a recent study. New research shows that contrary to previous scientific opinion, progressive lung damage in CF patients can begin as early as infancy even though lung function shortly after diagnosis is normal.” View full resource at eurekalert.org
Most Recently Shared on December 5, 2008 at 5:34 am By:
AAAS Intervention in infants with cystic fibrosis key to slowing progression http://tinyurl.com/6rfqkp
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