61. Cystic Fibrosis Symptoms, Diagnosis, Treatments And Causes - WrongDiagnosis.com Cystic Fibrosis information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis. http://www.wrongdiagnosis.com/c/cf/intro.htm

62. Cystic Fibrosis: Cystic Fibrosis (CF): Merck Manual Home Edition Cystic fibrosis is a hereditary disease that causes certain glands to produce abnormal secretions, resulting in tissue and organ damage, especially in the lungs and the http://www.merck.com/mmhe/sec23/ch287666/ch287666a.html

63. Cystic Fibrosis Nurses: The International Specialist Group Organization whose goals include setting and promoting high standards of nursing practice in the treatment of persons with Cystic Fibrosis. http://www.cfnurses.net

T H E I N T E R N A T I O N A L N U R S E S P E C I A L I S T G R O U P - C Y S T I C F I B R O S I S c/o Valerie Hall, Northern Ireland Regional Adult CF Centre, Belfast City Hospital, Lisburn Road, Belfast BT97AB, UK. email: valerie.hall@belfasttrust.hscni.net Telephone: 0044 2890263353 Comments, suggestions, ideas ? Send us an email Last update: March 2009 Webmaster: Filippo Festini Visitors:

64. UK Cystic Fibrosis Database The UK CF Database in Dundee closed in 2007. Each clinic received a full copy of data for all their patients. Anonymised UK data were sent to the CF Trust and Anonymised http://www.cystic-fibrosis.org.uk/

UK Cystic Fibrosis Database Home Background Annual Report Publications ... User Support The UK CF Database in Dundee closed in 2007 Each clinic received a full copy of data for all their patients. Anonymised UK data were sent to the CF Trust and Anonymised Scottish data to NSD Our group next developed a European demographic CF registry with data for over 29000 patients from 35 countries (see www.lancet.com/audio and select from Audio Archive the podcast for March 20, 2010 - Comparison of EU and non-EU cystic fibrosis registries. ). For all subsequent publications or for further information about the European demographic CF registry, please contact Dr Anil Mehta, a.mehta@dundee.ac.uk Background User Support Request For Data ... University of Dundee Created and Maintained by: N. Mehta Privacy Page Last Updated: 2 April 2010

65. Cystic Fibrosis Victoria Information about Cystic Fibrosis and the organisation, online chat room and message board. http://www.cfv.org.au

66. Cystic Fibrosis, Philips Respironics Information on Cystic Fibrosis from Respironics Cystic Fibrosis. Causes and Effects of CF Symptoms of CF. In cystic fibrosis (SISStick fy-BROH-sis), or CF, an imbalance of http://cysticfibrosis.respironics.com/

Home About Us Calendar of Events Careers ... Resources Cystic Fibrosis Causes and Effects of CF Symptoms of CF In cystic fibrosis (SISS-tick fy-BROH-sis), or CF, an imbalance of salt causes the lungs to fill with a thick, sticky mucus. The mucus interferes with breathing and encourages growth of bacteria. CF may also affect other organs, including the digestive system and the reproductive system. CF is a genetic disease caused by a mutation in the body's DNA and because children can inherit this mutation from their parents. CF affects about 1 in 3,500 births in the U.S. Many more people are symptomless carriers of the gene as many as 1 in 20 Americans. CF is far more prevalent in Caucasian-Americans, affecting 1 in 2,000 to 3,000 births. It is less common in African-Americans (1 in 15,000 to 17,000 births) and Asian-Americans (1 in 31,000 to 100,000 births). If a carrier of CF has a child with a person without the mutation, that child may be a carrier, but will not have the disease. Children can only get the disease when both parents are carriers, or one has CF. Treatment for CF has improved enormously. In the 1960s, life expectancy of children with CF was less than 8 years. Today 50 percent of CF sufferers are living into their late 30s or longer, some even into and past their 50s.

67. Welcome | Cochrane Cystic Fibrosis And Genetic Disorders Group An international network of health care professionals, researchers and consumers preparing, maintaining, and disseminating systematic reviews of randomised control trials in the treatment of cystic fibrosis and other genetic disorders. http://www.liv.ac.uk/CFGD/

Cochrane Cystic Fibrosis and Genetic Disorders Group Welcome Activities of the Group are co-ordinated by its Editorial Base, located within the Department of Child Health, University of Liverpool and based at Alder Hey Children's NHS Foundation Trust, Liverpool, United Kingdom. Published reviews and protocols On Issue 10, 2010 of The Cochrane Library we have published one new review 'Antibiotic adjuvant therapy for pulmonary infection in cystic fibrosis'. We have also updated the following reviews: Phytomedicines (medicines derived from plants) for sickle cell disease Treatments for priapism in boys and men with sickle cell disease Ursodeoxycholic acid for liver disease In total the Group has 94 reviews and 18 protocols published on Issue 10, 2010 of The Cochrane Library. There are also 10 registered titles currently progressing to protocol status. The production of these reviews involves a network of almost 550 authors, consumers and referees throughout the world. We very much welcome interest from new consumers, referees and potential reviewers. Further information can be obtained by contacting the group. Regularly updated evidence-based healthcare databases User guides Access options Page last updated: Tue 26th Oct 2010 10:54:41 CEST Search Current news at The Cochrane Collaboration Launch of the Safe Motherhood Initiative Evidence Aid for water safety and water related diseases Live broadcast from Keystone 21 October: "Can early stopped trials result in misleading results of systematic reviews?"

68. Cystic Fibrosis - Definition Of Cystic Fibrosis In The Medical Dictionary - By T Cystic Fibrosis Definition. Cystic fibrosis (CF) is an inherited disease that affects the lungs, digestive system, sweat glands, and male fertility. http://medical-dictionary.thefreedictionary.com/cystic fibrosis

69. Cystic Fibrosis Services, Inc. - Home A subsidiary of the Cystic Fibrosis Foundation in the United States, and a national pharmacy that offers minimal-cost medications to individuals with the disease. http://www.cfservicespharmacy.com/

About Us Meet Our CFS Staff Contact Us Today is Sunday, November 14, 2010 www.CFServicesPharmacy.com Home Cystic Fibrosis Services FAQs Cystic Fibrosis Community Support Cayston (Aztreonam For Inhalation) CF Services Products and Prices Vitamax® CF Multivitamins MedlinePlus Health Info. Drug Information Look-up CFS Medication Backorders CFF Great Strides 2010 Insurance Participating Provider Cystic Fibrosis Scholarships CF Patient Assistance Programs CF Legal Information Hotline CFF Signature Events Calendar CF Clinical Research and Trials CF Family Education Day Schedule Cystic Fibrosis Patient Education CF Educational Literature CF Pharmacy Reminder HomeLine Newsletter Español Donate News Research Volunteer Visit Our COMMUNITY PARTNERS Our Service Pledge Cystic Fibrosis Services Pharmacy is committed to providing customers and the cystic fibrosis community with world-class service and support. Therefore, we pledge... To always provide you with prompt and courteous customer service... Read More! Have Your Heard? Cystic Fibrosis Services Pharmacy Now Has Case Managers! Cystic Fibrosis Patient Assistance Programs ... Products and Prices Sally S. wants to spell it out for you: We feel so very fortunate to have Cystic Fibrosis Services on our side, on our team, and available to us as we manage Cystic Fibrosis on a daily basis.

70. Cystic Fibrosis Symptoms, Causes, Tests And Treatment For Cystic Fibrosis - From What is cystic fibrosis? Get information on symptoms, risk factors, and treatments for cystic fibrosis. http://children.webmd.com/tc/cystic-fibrosis-topic-overview

71. Fibrose Kystique/Cystic Fibrosis CPAFK/ACFCQ Non-profit community organization whose primary mission is to improve quality of life for persons with cystic fibrosis in Quebec. Information about CF for persons who have the disease, as well as their families, spouses, and caregivers. http://www.acfcq.qc.ca

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72. Cystic Fibrosis In Australia Welcome to the Cystic Fibrosis National Website. Cystic Fibrosis Australia assists member organisations to achieve common objectives by developing national......Default Meta http://www.cysticfibrosis.org.au/

Skip Navigation Home Cystic Fibrosis in Australia Welcome to the Cystic Fibrosis National Website Cystic Fibrosis Australia assists member organisations to achieve common objectives by developing national education programs and collecting and distributing information about Cystic Fibrosis (CF) at national and international levels. CF member organisations direct their activities to the provision of high quality health and welfare services to children and young adults with CF and their families. Donate Now We rely on donations to further research into CF and to provide services for children like Kalan living with CF. Help people live with Cystic Fibrosis by making a contribution today. 65 Roses Day is the national awareness and fundraising day for Cystic Fibrosis in Australia and falls on Friday 28 May 2010. To find out how you can be involved ..... more info State/Territory Organisations Your local organisation has a number of support programs available to assist to children and young adults with CF and their families. WA VIC TAS SA ... ACT Latest News 01 Nov 2010 CFA Cystic Fibrosis Australia Lottery on NOW 27 Sep 2010 NSW Christmas Cards are now ON SALE!!

73. Cystic Fibrosis | Baby | March Of Dimes Cystic fibrosis (CF) is an inherited disease that affects the lungs and digestive system. Most affected individuals survive into their late 30s. There is currently no cure. http://www.marchofdimes.com/professionals/14332_1213.asp

74. Cystic Fibrosis Worldwide Is An Organization Representing The CF Community With Organization seeking to aid people born with cystic fibrosis around the globe. Includes information on the disorder, programs, publications, fundraising, member associations and the CFW Network. http://www.cfww.org/

/*********************************************** * gAjax RSS Pausing Scroller- (c) Dynamic Drive (www.dynamicdrive.com) * Visit http://www.dynamicdrive.com/ for full source code ***********************************************/ /*********************************************** * All Levels Navigational Menu- (c) Dynamic Drive DHTML code library (http://www.dynamicdrive.com) * This notice MUST stay intact for legal use * Visit Dynamic Drive at http://www.dynamicdrive.com/ for full source code ***********************************************/ About Us Programs Member Associations Publications ... World Health Organization Your donations at work! Current Projects: Capacity building Program Education Program Our Achievements CFW Newsletter Visit the CFW Newsletter Library English Nederlands Deutsch Magyar ... Slovenčina Latest articles / translations Experiencia Personal: El arte de la actitud Medicina: ¿Terapia de células madre para la fibrosis quística? Consigli riguardo la fibrosi cistica: In viaggio con la Fibrosi Cistica Un País en Primer Plano: ASOCIACIONES NACIONALES: ¿Cómo es que “65 Rosas” se convirtió en el logotipo de la fibrosis quística?

75. Protein Structure Central To Cystic Fibrosis Solved Explains which protein is involved, how CF occurs, and how the information could help in developing treatment. From the Berkeley Lab and University of California at Berkeley. http://www.lbl.gov/Science-Articles/Archive/abc-cystic-fibrosis.html

76. Jake's Cystic Fibrosis Page Cystic Fibrosis Page with the CFAM newsletter. http://www.angelfire.com/mo2/cf/index.html

Jake's Cystic Fibrosis Page Please Visit My Links Page My Links My Bio CFAM Newsletter My Little Nephew Fritz ... CF Chat Room Hello my name is Jake Shasserre. I have had Cystic Fibrosis ever since I was born. This page was made to the help people learn what the diesease is and how to fight it. Alright people im back. Its been to long since I have updated this. I will make my best effort to get it done within the next couple weeks. So bear with me. Thanks Jake's Cystic Fibrosis Page How did you learn about my page? Friend Family Internet Search Link Other This The Cystic Fibrosis Ring site owned by Jake Shasserre Previous Next Random Site ... List Sites Want to join the ring? Click here for info Sign My Guestbook View My Guestbook Email: jake_the_snakers@hotmail.com

77. Cystic Fibrosis What is cystic fibrosis? Cystic fibrosis (CF) is an inherited (genetic) condition that affects the way salt and water move in and out of cells. http://www.chp.edu/CHP/Cystic Fibrosis

skip to the content For Clinicians For Parents For Teens ... Events and Classes Our Services Home Our Services Clinical Services Hillman Center for Pediatric Transplantation ... Cystic Fibrosis Cystic Fibrosis What is cystic fibrosis? Cystic fibrosis (CF) is an inherited (genetic) condition that affects the way salt and water move in and out of cells. This, in turn, affects glands that produce mucus, tears, sweat, saliva and digestive juices. Normally, the secretions produced by these glands are thin and slippery, and help protect the body's tissues. In people with cystic fibrosis, the secretions are abnormally thick and sticky, so that they don't move as easily. Instead of acting as lubricants, these thicker secretions may clog tubes, ducts and passageways throughout the body. Cystic fibrosis also causes increased salt in sweat on the skin. Who gets cystic fibrosis? Cystic fibrosis affects both males and females; approximately 30,000 people in the United States have been diagnosed with the condition. The greatest risk factor for cystic fibrosis is a family history of the disease, especially if either parent is a known carrier. The gene that causes cystic fibrosis is recessive. This means that in order to have cystic fibrosis, children must inherit two copies of the gene, one from each parent. If a child inherits only one copy, he or she won't develop cystic fibrosis. However, that child will still be a carrier, and might pass the gene on to his or her own children. People who carry the cystic fibrosis gene are healthy and have no symptoms of disease. In fact, it's estimated that as many as 10 million people may be carriers of a cystic fibrosis gene and not know it. If both parents carry a defective cystic fibrosis gene, each pregnancy has a 25 percent chance of producing a child with cystic fibrosis.

78. CYSTIC FIBROSIS FOR KIDS This site is for children with cystic fibrosis designed by a man from the Netherlands with CF. http://members.tripod.com/~jtatton/index.html

Build your own FREE website at Tripod.com Share: Facebook Twitter Digg reddit document.write(lycos_ad['leaderboard']); document.write(lycos_ad['leaderboard2']); Welcome to Cystic Fibrosis for KIDS !!! :) I am your host my name is William. Just like you I have Cystic Fibrosis. I know that much of Cystic Fibrosis that all the people I know call me Dr.Bob . On the next pages I'm going to tell you everything I know about Cystic Fibrosis. The good thing is , I'm not going to give you shots, IV's or anything so come along and follow me. Dr.Bob has many, many friends on the internet, and 3 nurses that help me with everything i don't know (even a doctor doesn't know everything). I'm William and I live in The Netherlands. That country is located between Germany and Belgium, look on a world map for that . I'm a 39 years old man and have 1 brother with Cystic Fibrosis and 1 sister without it. Sometimes I really wish I didn't have Cystic Fibrosis and I bet you feel the same. Still I know it will never go away, no matter how hard I wish. WELCOME TO YOUR OWN WEBSITE , CLICK ON THE BUTTONS BELOW.

79. Cystic Fibrosis - Symptoms, Treatment And Prevention of Cystic Fibrosis; Causes and Risk Factors of Cystic Fibrosis......Symptoms, Treatment and Prevention of Cystic Fibrosis Definition of Cystic Fibrosis; http://www.healthscout.com/ency/68/222/main.html

80. AussieBillaBong Single mothers fight with Cystic Fibrosis and Marfans syndrome, affecting one lung. http://www.angelfire.com/ms2/CysticFibrosisMarfan/index.html

G�day, My name is Kathryn,an aussie, I am a single parent with 2 children, Tristan aged 17 and jasmine aged 8 years. 8 years ago I was first diagnosed virtually straight after jasmines birth, with Osteopenia �85% density in my bones, then came Marfan�s syndrome, Bronchiectasis, Emphysema, Cystic Fibrosis and now an Ulcer is the lower throat. The pages consist of my illnesses, my feelings, emotions, and the stress I am going through. The Rose was chosen by Cystic Fibrosis (CF) Victoria as the Australian symbol for CF. The rose has endured throughout history as the symbol of abiding love. It is also linked to CF because of the story of a young boy who, in an effort to describe his sister's Cystic Fibrosis, mis-pronounced it as �65 Roses�. On my support page, I am hoping to collect 65 roses (animated)** The roses have been broken up and put on different pages to download quicker**. If you have any or know some websites that have some please email me. Unfortunatly you can only access the "roses" via the support and guestbook page only. Please bookmark this site, and come back often.

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