21. Canadian Cystic Fibrosis Foundation http://www.ccff.ca/

22. HHMI: Scientists & Research HHMI investigators have been involved in many important recent advances, from the discovery of genes related to cystic fibrosis, obesity, and other diseases, to new insights about how human cells develop or communicate. http://www.hhmi.org/home/research/index.html

HHMI Policies The Office of the General Counsel and its role in administering the policies that govern the work of the Institute. More HHMI-NIH Research Scholars Learn about the HHMI-NIH Research Scholars Program, also known as the Cloister Program. More Janelia Farm Research Campus Learn about the new HHMI research campus located in Virginia. More Catalyzing Discovery The promise embodied by Hughes's sweeping statement took decades to be fully realized, decades of challenge and risk for a philanthropy that has evolved in ways Hughes might never have imagined. Today, HHMI is a recognized leader in biomedical research. Discoveries made in HHMI laboratories are fundamentally changing the way we view the world. Ideas born in Hughes laboratories are also improving the understanding of some of society's most vexing health problems, including AIDS, cardiovascular disease and diabetes. At HHMI, the engines of discovery are powered by more than 300 HHMI investigators who direct Institute research laboratories on the campuses of universities and other research organizations throughout the United States. The Institute also supports scientists through its grants programs. The HHMI professors are a group of researchers with a passion for teaching. They are using their HHMI grants to develop innovative methods of communicating the beauty of science to undergraduate students. In addition, HHMI supports a select group of international research scholars who hail from institutions and universities all over the globe. These scholars are expanding research in countries where funds may be limited.

23. Cystic Fibrosis Trust Aiming To Understand, Treat And Cure Cystic Welcome to the cystic fibrosis Trust homepage http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

24. Canadian Cystic Fibrosis Foundation The Canadian cystic fibrosis Foundation (CCFF) is a Canadawide health The Foundation’s primary objective is to fund cystic fibrosis research and care. http://www.ccff.ca/home.asp

About the Foundation How to donate Organ Donation CARSTAR presents FrightLites Our Celebrity Patron ... Volunteering Update: var mvName = '%2Fcontent%2F%2E%2E%2Fmedia%2FPSA%5FLaundry%5FEN%2Ewmv'; Video Presentation Click here to view one of our public service announcements. (WMV 1.34 MB). Extranet Contact Us Français Information designed for you Persons with CF Media Room New Insight Into Pseudomonas aeruginosa ... Shinerama Charitable Registration No. 10684-5100 RR0001.

25. Cystic Fibrosis Nurses: The International Specialist Group Includes objectives, constitution, officers, events, meeting archives, and discussion forum. http://www.cfnurses.net/

UK CF Nurse Specialist Group's Consensus Standards for the Nursing management of CF 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 Susan Madge, Department of Cystic Fibrosis, Royal Brompton Hospital, Sydney Street, London SW3 6NP, UK. Tel +44 207 352 8121 ext 4053, bleep 6013 email: S.Madge@rbh.nthames.nhs.uk Comments, suggestions, ideas ? Send us an email Last update: August 26, 2005 Webmaster: Filippo Festini, RN, BA, BSN Visitors:

26. Respiratory Medicine Includes information on asthma, copd, cystic fibrosis, telemedicine, spirometry, scientific publications, meetings and pulmonary medicine. http://users.pandora.be/spirometrie/

topics publications links news ... contact Wellcome ! This site is dedicated to respiratory medicine and may be of interest to you if you are a respiratory patient, a General Practitioner, a Specialist or just interested in Respiratory Medicine. We will provide you with information on respiratory diseases like asthma and COPD , respiratory diagnostics like spirometers , and interesting articles and links to other sites containing valuable information in the field of respiratory medicine. Please visit us frequently as we plan to keep this site updated. If you have an interesting article or link you would like to see here, feel free to contact us. Have fun! This site gives information on medical issues in the field of respiratory medicine to the author's best knowledge. If you feel incorrect information is given, please contact us with your remarks.

27. Pathophysiology And Management Of Pulmonary Infections In Cystic Pathophysiology and Management of Pulmonary Infections in cystic fibrosis Ronald L. Gibson , Jane L. Burns and Bonnie W. Ramsey http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

28. Cystic Fibrosis Research, Inc. (CFRI) News about CF research. Site also has a newsletter available. http://www.cfri.org/

29. PUSH4Johnny.com Pictures and articles about his life and his battle with cystic fibrosis. Includes poetry, a video tribute and information about the Bowl for Breath fundraising drive. http://push4johnny.com/

Welcome to: PUSH4Johnny.com P ray U ntil S omething H appens For the Cure for C.F. Updated 8/23/05 Another life claimed by C.F. This Morning Friday, August 12, 2005 at 1:05 am Maggie passed away, and is now in the hands of the Lord. Maggie has claimed her victory in Jesus! Our hearts and our prayers are with the Mackey Family in this time of need. We need to P.U.S.H for a cure for this horrible disease! P.U.S.H. Pray Until Something Happens We love you Maggie and we will see you soon in Heaven! Great News! A Young Man With Cystic Fibrosis Michael Livingston On August 6th 2005 Michael Livingston received a new set of Lungs! He was released from the hospital this last Friday. He is doing very well so far, but we should still keep him in our prayers as he has a long recovery ahead. The transplant took place at the University of San Diego. Thank you Lord for the Great Doctors. We are so excited to here the great news Michael From; John, Esther and Trisha (Johnny's Family)

30. Cystic-L - Cystic Fibrosis Info Support CYSTICL is a free email service dedicated to the exchange of information and support specific to cystic fibrosis. Members include people with CF and http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

31. -+=CFRI=+- Cystic Fibrosis Research, Inc. http://www.cfri.org/home.htm

32. Alice Martineau Official site. Photos, forum, her music, and information about cystic fibrosis, from which she died. http://www.alicemartineau.com/

33. Cystic Fibrosis Information And Resources For Patients, Relatives And Medical Pr Provides free information to professionals involved with the treatment of cystic fibrosis. An open access section is also available to both patients and http://www.cysticfibrosismedicine.com/

Best viewed with Internet Explorer ver 5.5 or above at a resolution of 800x600 This site needs Javascripting and Cookies turned on for optimum browsing articles

34. Solvay, Berna Biotech Agree Jv For Cystic Fibrosis Vaccine Aerugen has agreed a joint venture with Swiss firm Berna Biotech Ltd for the marketing, distribution and licensing of cystic fibrosis vaccine Aerugen. http://tmsyn.wc.ask.com/r?t=an&s=hb&uid=24312681243126812&sid=343126

35. Cystic Fibrosis Mutation Database Database of cystic fibrosis mutations plus other relevant information on these mutations. http://www.genet.sickkids.on.ca/cftr/

36. Cystic Fibrosis Gene Therapy: Oxford Gene Medicine Focused on the development gene therapies for diseases of the airway, such as asthma, lung cancer and in particular, cystic fibrosis (CF). Work includes formulation development, reagent production, preclinical testing, and human clinical trials. http://users.ox.ac.uk/~genemed/default.htm

Click to enter Cystic Fibrosis is one of the most common genetic diseases. Research is directed towards developing a treatment for the pulmonary symptoms of cystic fibrosis using, primarily, non-viral (plasmid/liposome) delivery systems for gene transfer. Laboratory studies focus on understanding the factors which limit gene transfer and developing improved gene transfer reagents and delivery methods. These reagents are tested in transgenic mouse models prior to entering optimal formulations into an ongoing clinical trials programme

37. Cystic Fibrosis Australia - Education And Research Organisation - CFA - National cystic fibrosis Australia CFA is a national body comprising member State Associations. It assists the member organisations to achieve common objectives by http://www.cysticfibrosisaustralia.org.au/

Home About Us/Aims and Objectives Events List Current Newsletter ... Contacts and Links "I want everyone to know about Cystic Fibrosis. At least 30% of teenagers with the disease pass away and I have lost many childhood friends from the condition" Emmah Money - Cystic Fibrosis Ambassador and 2005 Girlfriend of the Year winner. Emmah Money's Inspirational Story - Living with CF was televised during the week commencing August 8 2005 on ABC's Australian Story Click here to for Australian Story article and transcript Sunday 11th September Llewellyn Hall, Canberra School of Music 6th Australian and New Zealand Cystic Fibrosis Conference The 6th Australian and New Zealand Cystic Fibrosis Conference was held in Adelaide 20-23rd August 2005. 380 Delegates attended our unique style of conference which, consisted of medical, scientific, allied health and lay programs. A diverse range of speakers from Australia and overseas were well received by the delegates. The theme "CF People and Science" gave a wonderful overview of the new thoughts and developments, which have come about in the past two years in all areas.

38. A-Z Medical Directory & Electronic Journal For AIDS, Cancer, Cystic Fibrosis And AZ listings for over 4,000 treatment centers, research institutes, charities and hospitals in the areas of AIDS/HIV, Diabetes, cystic fibrosis and cancer. http://www.cellscience.com

directory for health care, charity and research Cancer Cystic Fibrosis Diabetes Journal ... Nervous Disorders WWW Cellscience

39. Cystic-L - Cystic Fibrosis Info & Support CYSTICL is a free email service dedicated to the exchange of information and support specific to cystic fibrosis. Members include people with CF and those http://cystic-l.org/

What's New The CF Shop Thunder-Bay Productions What's New The CF Shop Thunder-Bay Productions

40. Genetic Disorders: The Links To Diet Explores the role of diet in birth defects and genetic disorders. Includes nutritional links to disorders such as Down syndrome, cerebral palsy, homocystinuria, and cystic fibrosis. http://www.ctds.info/genetic_disorders.html

Con nective Tissue Disorder Home Search Site Map ... Links Genetic Disorders The Links to Diet Read my Contents: Overview Genetic Disorders and Birth Defects Treatable Through Diet Prenatal Nutrition and Birth Defects Genetic Disorders, Birth Defects and Logic ... General Information on Genes, Nutrition and Disease Overview Many researchers and support groups state that birth defects and genetic disorders, especially connective tissue disorders such as Marfan syndrome osteogenesis imperfecta and Ehlers-Danlos syndrome , can't possibly be cured through diet because they are inherited genetic disorders. This conclusion is invalid simply because many birth defects and inherited genetic disorders have been found to be improved, or even cured, through diet. The old school of thinking that a birth defect or inherited disorder had to be caused by a single gene is no longer widely held in medical circles. The breakthrough concept in research is that many birth defects and inherited disorders are influenced by both genes and environmental factors, especially nutrition. Genes may make people susceptible to certain defects and disorders, but they are often only a part of the picture. "Genes are not necessarily destiny. They are influenced by the chemistry of what we consume." - article on

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