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Topic: Fibrosis



  
 MSN Encarta - Cystic Fibrosis
Using a procedure called chest physical therapy or postural drainage, caregivers of people with cystic fibrosis repeatedly and vigorously pound on the patient’s back and chest to dislodge mucus obstructing the airways.
Although no cure has yet been found, cystic fibrosis presents one of the most promising areas of research in modern medicine.
Teenagers with cystic fibrosis may grow slowly and enter puberty later than their peers.
http://encarta.msn.com/encnet/refpages/RefArticle.aspx?refid=761567047   (1098 words)

  
 Pulmozyme - Cystic Fibrosis information and disease education
According to the U.S. Cystic Fibrosis Foundation, the median average life expectancy for patients with cystic fibrosis is 31 years.
Launched in 1994, Pulmozyme was the first new therapeutic drug for the management of cystic fibrosis in over 30 years.
Cystic fibrosis affects other organ systems as well, especially the digestive tract and reproductive organs.
http://gene.com/gene/products/information/opportunistic/pulmozyme/index.jsp   (291 words)

  
 Cystic Fibrosis Information
CFRI Research:CFRI's mission is to fund cystic fibrosis research and to offer educational and support programs for people with CF and their families.
Cystic Fibrosis Foundation:The Cystic Fibrosis Foundation (CFF) was established in 1955 to raise money for research to find a cure for cystic fibrosis (CF) and to improve the quality of life for the 30,000 children and young adults with CF.
The Foundation works to heighten awareness of cystic fibrosis and to provide a better quality of life for those affected by cystic fibrosis.
http://pw2.netcom.com/~yourman/webdoc1.htm   (637 words)

  
 Cystic fibrosis
Many pancreatic enzymes involved in the breakdown and absorption of fats in the intestine are absent, causing malabsorption (inadequate absorption of nutrients from the intestinal tract) and malnutrition.
A recent study showed that the pain reliever ibuprofen may slow lung deterioration in some children with cystic fibrosis.
Risk factors include a family history of cystic fibrosis or unexplained infant death.
http://www.shands.org/health/information/article/000107.htm   (591 words)

  
 Fibrosis
Women who had no history of HRT also tended to have more advanced fibrosis and faster fibrosis development compared to those who had been previously prescribed the therapy, Di Martino and his colleagues found.
Discordances of at least 1 point were observed in 52% and of 2 points in 22% of patients.
Papatheodoridis and his colleagues found fibrosis improved in about 17 percent of the treated patients, overall, compared to just 4 percent of those who didn't receive
http://janis7hepc.com/fibrosis1.htm   (4034 words)

  
 Cystic Fibrosis
Cystic fibrosis (CF) is a cruel and deadly disease affecting the respiratory system, digestive system, endocrine system, and reproductive system.
Carnitine metabolites in infants with cystic fibrosis: a prospective study.
Hodson ME. Aerosolized Dornase Alfa (rhDNase) for therapy of cystic fibrosis.
http://www.thorne.com/altmedrev/fulltext/cystic.html   (5065 words)

  
 Cystic Fibrosis
While still in her pajamas, her parents clap her back and chest for at least 20 minutes to help clear her lungs of the thick mucus that sometimes makes it difficult for her to breathe.
The good news is that newer medicines are more effective and help kids with CF recover more quickly.
Every day when she wakes up, Lisa begins to deal with a condition she's known all her life - cystic fibrosis (say: sis-tik fi-bro-sus).
http://www.kidshealth.org/kid/health_problems/heart/cystic_fibrosis.html   (1069 words)

  
 What is Pulmonary Fibrosis?, What are the symptoms, prevalence and treatments for the disease?
There are currently no effective treatments or a cure for Pulmonary Fibrosis.
There are a number of new trials testing drugs to treat Pulmonary Fibrosis.
There is a growing body of evidence which points to a genetic predisposition.
http://www.pulmonaryfibrosis.org/ipf.htm   (359 words)

  
 CBBB Wise Giving Alliance
Cystic Fibrosis Foundation maintains a network of 10 research and development program centers, 8 therapeutic development centers (including drug and gene therapies), and over 110 care centers across the United States that are dedicated to the study, treatment, and cure of cystic fibrosis.
"to assure the development of the means to cure and control cystic fibrosis and to improve the quality of life for those with the disease."
This affiliate operates the CF Clinical Research and Drug Development and Discovery Programs.
http://www.give.org/reports/care_dyn.asp?163   (708 words)

  
 Voltage-dependent Gating of the Cystic Fibrosis Transmembrane Conductance Regulator Cl- Channel -- Cai et al. 122 (5): ...
Asymmetric structure of the cystic fibrosis transmembrane conductance regulator chloride channel pore suggested by mutagenesis of the twelfth transmembrane region.
Permeability of wild-type and mutant cystic fibrosis transmembrane conductance regulator chloride channels to polyatomic anions.
Identification and regulation of the cystic fibrosis transmembrane conductance regulator-generated chloride channel.
http://www.jgp.org/cgi/content/full/122/5/605   (7457 words)

  
 Biospace.com
The Phase II study enrolled 125 patients who were treated at 26 CF centers in the U.S., and the Company believes that it represents the largest prospective, randomized, double blind, and dose-ranging trial conducted to evaluate the safety and efficacy of enzyme replacement therapy in the treatment of CF patients with pancreatic insufficiency.
Cystic Fibrosis Foundation Therapeutics, Inc. (CFFT) the nonprofit drug discovery and development affiliate of the Cystic Fibrosis Foundation, is supporting this pivotal trial with study-specific funding of up to $2.35 million in milestone-driven, matching funds through a Therapeutics Development Award.
European Medicines Evaluation Agency Grants PTC Therapeutics, Inc. Orphan Drug Designation For PTC124 For The Treatment Of Duchenne Muscular Dystrophy And Cystic Fibrosis
http://www.biospace.com/news_rxtarget.cfm?RxTargetID=63   (829 words)

  
 Cystic Fibrosis / Family Village
The The Cystic Fibrosis Foundation (CFF) was established in 1955 to raise money for research to find a cure for Cystic Fibrosis (CF) and to improve the quality of life for the 30,000 children and young adults with the disease.
Through its research and clinical programmes, the Foundation helps to provide outstanding care for affected individuals, while pursuing the quest of a cure or control for the disease.
The Foundation provides information and training for scientific and health care personnel and distributes educational material for patients, families, and the general public regarding CF.
http://www.familyvillage.wisc.edu/lib_cysf.htm   (552 words)

  
 Breathing Room: The Art of Living with Cystic Fibrosis
facilitates candid and open communication between adults with Cystic Fibrosis, supports the development of a community of adults with CF and provides education and insight for families, caregivers, and medical professionals who impact our lives.
It is intensely personal and many of us do not always have an opportunity to share how our spirituality is affected by having cystic fibrosis.
When we spoke that day, he kept talking about "a sense of service" - and feeling the desire, even the need, to give back (in our case) to the cf community.
http://www.thebreathingroom.org   (296 words)

  
 Cystic Fibrosis Center Portal, Cincinnati Children's Hospital Medical Center
The Cystic Fibrosis Center Portal is not intended to replace the personal relationships you have with your caregivers.
The Cystic Fibrosis Center Portal is one more way to keep you connected with us and help to ensure excellent outcomes for your child.
Because we want to provide you with the best information on your child's care, the CF Center Portal is continuously being updated and expanded.
http://www.cincinnatichildrens.org/svc/alpha/c/cf/portal.htm   (603 words)

  
 genome.gov Learning About Cystic Fibrosis
Since CF cannot be treated before birth, the purpose of prenatal testing is to prepare parents to care for a baby with special health needs, or to make a decision about terminating the pregnancy.
Genetic Research May Lead to New Drugs to Treat Cystic Fibrosis
Another research breakthrough offers a promising approach to treating cystic fibrosis.
http://www.genome.gov/10001213   (1015 words)

  
 CFW is an organization representing the CF community with a worldwide mandate.
Cystic Fibrosis drugs are available to all CF patients affected by Hurricane Katrina regardless of their ability to pay.
It gives CF Nurses the opportunity to develop their ideas within the stimulating research environment provided by CF centres of excellence.
This scholarship, supported by Chiron, aims to encourage the exchange of best practice amongst Nurses working in centres of cystic fibrosis (CF) patient care.
http://www.cfww.org   (386 words)

  
 Cystic Fibrosis Resource Center - HealingWell.com
Questions and answers about the symptoms of CF and what you should do if you suspect your child may have Cystic Fibrosis.
Find medical journal articles, industry news, and wire releases for healthcare professionals and savvy consumers on Cystic Fibrosis and many other topics.
Get current news on treatments, procedures and research, and watch doctor produced video updates on Cystic Fibrosis.
http://www.healingwell.com/cysticfibrosis   (274 words)

  
 Pulmonary Fibrosis Information
In an open lung biopsy, a chest surgeon makes cuts between the ribs in the chest and removes small pieces of tissue from several places in the lungs.
The quality of your life will largely depend on your perspective and interpretation of life itself.
I will try to cover some of the more psychological aspects in the
http://www.california.com/~emile/Index.html   (2139 words)

  
 Cystic Fibrosis News
Bucks County Courier Times Ten-year-old Jessica Franklin takes more than 50 pills a day, uses inhalers and performs one physical therapy session in the morning and another at night just to keep her chest and...
K-State researchers designing better drug to treat cystic fibrosis
Chiron Corp. and Nektar Therapeutics Inc. said Wednesday that they have begun a late-stage trial of an experimental inhaled, powdered form of an antibiotic to treat certain lung infections in cystic fibrosis...
http://www.topix.net/health/cystic-fibrosis   (1091 words)

  
 The cystic fibrosis transmembrane conductance regulator (CFTR) inhibits ENaC through an increase in the intracellular ...
Boucher, R.C., Cotton, C.U., Gatzy, J.T., Knowles, M.R. and Yankaskas, J.R. (1988) Evidence for reduced Cl and increased Na permeability in cystic fibrosis human primary cell cultures.
New concepts of the pathogenesis of cystic fibrosis lung disease
the cystic fibrosis (CF) defect (Boucher et al.
http://emboreports.npgjournals.com/cgi/content/full/2/11/1047   (3337 words)

  
 Nederlandse Cystic Fibrosis Stichting
Andere namen voor Cystic Fibrosis luiden CF, taaislijmziekte, mucoviscidose, mucoviscidosis, cystische fibrose of kystische fibrose.
In het Engels duiden wij onze organisatie aan met Dutch Cystic Fibrosis Foundation, Dutch Cystic Fibrosis Organization, Dutch Cystic Fibrosis Organisation, Dutch CF Organization, Dutch CF Organisation of Dutch CF Association.
U vindt hier informatie over Cystic Fibrosis (CF), de NCFS, op vakantie gaan met CF, andere websites op het gebied van Cystic Fibrosis enz.
http://www.ncfs.nl   (149 words)

  
 EUROPEAN CYSTIC FIBROSIS SOCIETY
Membership of the society is open to any clinician or scientist actively engaged in CF research or CF care.
Mission Statement: The ECFS aims to achieve the best possible treatment and the highest quality of life for the patient with cystic fibrosis by the development and distribution of knowledge in the field of cystic fibrosis
Invitation to participate in a Pan European study on Pancreatitis in CF: Prevalence and Outcome
http://www.ecfsoc.org   (318 words)

  
 Barnes-Jewish Hospital - Cystic Fibrosis
That’s why Barnes-Jewish Hospital began the Adult Cystic Fibrosis program, as a complement to the excellent pediatric CF program at St. Louis Children’s Hospital, to treat patients with the latest therapies and improve their quality of life.
Directed by world-renowned pulmonologists, the Adult Cystic Fibrosis team at Barnes-Jewish Hospital uses an approach to treatment that brings together a specialized team including nurses, dietitians, social workers and counselors.
As Cystic Fibrosis patients mature, their medical, social, emotional and nutritional needs change.
http://www.barnesjewish.org/groups?NavID=338   (310 words)

  
 UK Cystic Fibrosis Gene Therapy Consortium
he UK has always been at the forefront of gene therapy for cystic fibrosis (CF) and the members of the Consortium have already demonstrated proof-of-principle of correction of the underlying defect in the airways of CF subjects.
The CF Trust funds medical and scientific research aimed towards understanding, treating and curing Cystic Fibrosis.
The UK Cystic Fibrosis Gene Therapy Consortium (UK CFGTC) is the unified research programme of the three leading gene therapy groups in the UK.
http://www.cfgenetherapy.org.uk   (425 words)

  
 MedlinePlus: Cystic Fibrosis
Nutrition and Cystic Fibrosis: Changes through Life (Cystic Fibrosis Foundation) - Links to PDF
Curcumin: Information for Patients and Families (07/01/2004, Cystic Fibrosis Foundation) - Links to PDF
Glutathione and Other Antioxidants: Information for Patients and Families (07/01/2004, Cystic Fibrosis Foundation) - Links to PDF
http://www.nlm.nih.gov/medlineplus/cysticfibrosis.html   (441 words)

  
 Cystic Fibrosis Symptom.com - Cystic Fibrosis foundations,  resources, symptoms, and information
Visit our Cystic Fibrosis News page, and get the latest news on research, treatments and other cystic fibrosis news related stories.
Many CF patients live a long full life well past expected lifespan of 40 years.
Many of the symptoms of Cystic Fibrosis can be treated with drugs or nutritional supplements.
http://www.cystic-fibrosis-symptom.com   (466 words)

  
 Cystic Fibrosis - Pulmonologychannel
Cystic fibrosis (CF) is the most common fatal, inherited disease in the United States (see Incidence).
We subscribe to the HONcode principles of the Health On the Net Foundation
CF causes the body to produce abnormally thick and sticky mucus in several different parts of the body, most prominently in the lungs and other parts of the respiratory system.
http://www.pulmonologychannel.com/cf   (1004 words)

  
 Pulmonary fibrosis definition - Medical Dictionary definitions of popular medical terms
Treatment involves the use of corticosteroids (such as prednisone) and/or other medications that suppress the body's immune system.
Our Pulmonary fibrosis Main Article provides a comprehensive look at the who, what, when and how of Pulmonary fibrosis
Interferon gamma-1b treatment may help patients with idiopathic pulmonary fibrosis who do not respond to corticosteroid therapy.
http://www.medterms.com/script/main/art.asp?articlekey=10871   (389 words)

  
 Cystic Fibrosis Adult Care: Consensus Conference Report -- Yankaskas et al. 125 (1 Supplement): 1 -- Chest
Of the 22,301 patients with CF in the 2000 Cystic Fibrosis Foundation
few decades in cystic fibrosis (CF) care more clearly than the
Unlike this latter benign condition, DIOS can rapidly
http://www.chestjournal.org/cgi/content/full/125/1_suppl/1S   (8977 words)

  
 Inhibition of cystic fibrosis transmembrane conductance regulator by novel interaction with the metabolic sensor ...
Inhibition of volume-regulated anion channels by expression of the cystic fibrosis transmembrane conductance regulator.
Welsh, M.J., and Smith, A.E. Molecular mechanisms of CFTR chloride channel dysfunction in cystic fibrosis.
ATP depletion induces a loss of respiratory epithelium functional integrity and down-regulates CFTR (cystic fibrosis transmembrane conductance regulator) expression.
http://www.jci.org/cgi/content/full/105/12/1711   (5877 words)

  
 Cystic Fibrosis Disease Profile
1936 - Fanconi refers to the previously nameless condition as "cystic fibrosis with bronchiectasis."
"Physiological Basis of Cystic Fibrosis: A Historical Perspective." Physiological Reviews 79 (1 Suppl.): S3-22.
Cystic fibrosis (CF) is a chronic, progressive, and frequently fatal genetic (inherited) disease of the body's mucus glands.
http://ornl.gov/sci/techresources/Human_Genome/posters/chromosome/cf.shtml   (997 words)

  
 Macromolecular Interactions and Ion Transport in Cystic Fibrosis -- Guggino and Banks-Schlegel 170 (7): 815 -- American ...
Correspondence and requests for reprints should be addressed to Susan Banks-Schlegel, Division of Lung Diseases, National Heart, Lung, and Blood Institute, Two Rockledge Center, Room 10018, 6701 Rockledge Drive, MSC 7952, Bethesda, MD 20892-7952.
Articles by Guggino, W. Articles by Banks-Schlegel, S. American Journal of Respiratory and Critical Care Medicine Vol 170.
Cystic fibrosis (CF) is a genetic disease caused by autosomal
http://www.ajrccm.org/cgi/content/abstract/170/7/815   (422 words)

  
 CysticFibrosis.com
Cystic Fibrosis affects the respiratory, digestive and reproductive systems.
Visit our skin health center for great products!
I have learned through the years, that having insight and foresight are two valuable tools to have while surviving an illness.
http://cysticfibrosis.com   (135 words)

  
 Cystic Fibrosis - Doctor's Guide to the Internet
Study Shows Intermittent Tobi Therapy Effective In Cystic Fibrosis Patients
New Orphan Drug May Be Effective Cystic Fibrosis Treatment
The latest medical news and information for patients or friends/parents of patients diagnosed with Cystic Fibrosis.
http://www.pslgroup.com/CF.HTM   (398 words)

  
 Cystic fibrosis - Genetics Home Reference
Other factors likely influence the course of the condition.
Cystic fibrosis is an inherited disease of the mucus glands that affects many of the body's organs.
Most people with cystic fibrosis also have digestive problems.
http://ghr.nlm.nih.gov/condition=cysticfibrosis   (724 words)

  
 Cystic Fibrosis Trust: Aiming to understand, treat and cure Cystic Fibrosis
A lot of people are beginning to be concerned about bird flu, and how it will affect those with Cystic Fibrosis.
The Cystic Fibrosis Trust is the UK's only national charity that funds research into treating and curing Cystic Fibrosis and to ensure appropriate clinical care and support for people with Cystic Fibrosis.
Cystic Fibrosis Trust: Aiming to understand, treat and cure Cystic Fibrosis
http://www.cftrust.org.uk   (311 words)

  
 New concepts of the pathogenesis of cystic fibrosis lung disease -- Boucher 23 (1): 146 -- European Respiratory Journal
New concepts of the pathogenesis of cystic fibrosis lung disease
New concepts of the pathogenesis of cystic fibrosis lung disease -- Boucher 23 (1): 146 -- European Respiratory Journal
Adult stem cells from bone marrow stroma differentiate into airway epithelial cells: Potential therapy for cystic fibrosis
http://erj.ersjournals.com/cgi/content/abstract/23/1/146   (550 words)

  
 Coalition for Pulmonary Fibrosis Welcome
Membership in the CPF is open to all individuals and organizations interested in promoting awareness of pulmonary fibrosis and in helping to advance pulmonary fibrosis education, patient support, treatment, and research.
The Coalition for Pulmonary Fibrosis (CPF) is a 501 (c) (3) nonprofit organization,founded in 2001 to further education, patient support and research efforts for pulmonary fibrosis, specifically idiopathic pulmonary fibrosis (IPF).
The CPF is governed by the nation's leading pulmonologists, individuals affected by pulmonary fibrosis, medical research professionals and advocacy organizations.
http://www.coalitionforpf.org   (277 words)

  
 Cystic Fibrosis Ibuprofen Laboratory
The Cystic Fibrosis Ibuprofen Laboratory provides ibuprofen analyses and therapeutic recommendations to physicians treating cystic fibrosis patients with ibuprofen.
Welcome to the Cystic Fibrosis Ibuprofen Laboratory !!!
The old URL for the Cystic Fibrosis Ibuprofen Laboratory (http://www.cwru.edu/orgs/CFIBUPLAB/cfibuplab.htm) will soon be changing.
http://www.cwru.edu/affil/CFIBUPLAB/cfibuplab.htm   (221 words)

  
 Cystic Fibrosis Message Board
Re: care of person with cystic fibrosis - Kelly 21:31:48 9/05/00 (
diet therapy for persons with cystic fibrosis - Michelle 22:16:27 4/12/00 (
Re: diet therapy for persons with cystic fibrosis - diane 01:14:37 8/11/00 (
http://www.healthboards.com/cystic-fibrosis   (4121 words)

  
 Pathophysiology and Management of Pulmonary Infections in Cystic Fibrosis -- Gibson et al. 168 (8): 918 -- American ...
The cystic fibrosis (CF) scientific community has orchestrated
Figure 8 from the Cystic Fibrosis Foundation Patient Registry
Organisms reported to the U.S. Cystic Fibrosis Patient Registry, 2001.
http://ajrccm.atsjournals.org/cgi/content/full/168/8/918   (8143 words)

  
 Utah Valley Institute of Cystic Fibrosis
about our work on glutathione therapy and cystic fibrosis.
We encourage all that are concerned about cystic fibrosis to participate in this forum, even if only as an observer.
Page to assist you in contacting the UVICF.
http://members.tripod.com/uvicf   (90 words)

  
 Cystic Fibrosis Information and Resources for patients, relatives and medical professionals
Cystic Fibrosis Information and Resources for patients, relatives and medical professionals
This site needs Javascripting and Cookies turned on for optimum browsing
http://www.cysticfibrosismedicine.com   (36 words)

  
 Lung Infections Associated with Cystic Fibrosis -- Lyczak et al. 15 (2): 194 -- Clinical Microbiology Reviews
cystic fibrosis (CF) is now recognized as a single disease whose
Population Structure, Antimicrobial Resistance, and Mutation Frequencies of Streptococcus pneumoniae Isolates from Cystic Fibrosis Patients.
Miller, M. B., Gilligan, P. Laboratory Aspects of Management of Chronic Pulmonary Infections in Patients with Cystic Fibrosis.
http://cmr.asm.org/cgi/content/abstract/15/2/194   (1754 words)

  
 Cystic Fibrosis
People with CF require treatment only when they have an attack.
The following statements test what you know about cystic fibrosis.
Fill out the test by choosing true or false, then press the submit button.
http://www.aarc.org/patient_education/iq_tests/cf/cf_form.html   (125 words)

  
 Cystic Fibrosis
Yourman Family CF site and Surviving Cystic Fibrosis
Recommended for teens and pre-teens ages 10 to 15 with CF and their families, STARBRIGHT Foundation, Explorer Series® CD-ROMs give seriously ill kids and teens a fun way to find out more about their health care.
- Cystic Fibrosis Research Inc. (CFRI), California, research and education
http://www.kumc.edu/gec/support/cystic_f.html   (354 words)

  
 Bone mineral density in Australian children, adolescents and adults with cystic fibrosis: a controlled cross sectional ...
individuals with cystic fibrosis (CF) although the pathogenesis
Guide to Bone Health and Disease in Cystic Fibrosis
Sternal fracture with fatal outcome in cystic fibrosis
http://www.thoraxjnl.com/cgi/content/abstract/59/2/149   (590 words)

  
 Cystic Fibrosis Information
Traveling tips for those who have CF (Added Sept.
Standards of care for patients with cystic fibrosis: a European consensus (Added Apr. 1, 2005)
Past and Future CF Conferences (Updated Dec. 29, 2004)
http://www3.nbnet.nb.ca/normap/CF.htm   (871 words)

  
 MedlinePlus: Pulmonary Fibrosis
Atlas of the Body: The Respiratory System -- Structure Detail (American Medical Association)
The primary NIH organization for research on Pulmonary Fibrosis is the National Heart, Lung, and Blood Institute
Interstitial Lung Disease and Pulmonary Fibrosis (American Lung Association)
http://www.nlm.nih.gov/medlineplus/pulmonaryfibrosis.html   (231 words)

  
 Pulmonary Fibrosis symptoms, causes, and treatment by MedicineNet.com
Most of these people have a condition called idiopathic pulmonary fibrosis (IPF) that does not respond to medical therapy, while some of the other types of fibrosis, such as nonspecific interstitial pneumonitis (NSIP), may respond to immune suppressive therapy.
Pulmonary Fibrosis symptoms, causes, and treatment by MedicineNet.com
Pulmonary fibrosis can be caused by many conditions including chronic inflammatory processes (sarcoidosis,
http://www.medicinenet.com/pulmonary_fibrosis/article.htm   (355 words)

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