41. ScienceDirect - Journal Of Cystic Fibrosis - List Of Issues cystic fibrosis disease information on symptoms, treatment and causesConcise factsheet on causes, symptoms and treatment of cystic fibrosis, this factsheet can also be downloaded in Acrobat format. http://www.sciencedirect.com/science/journal/15691993

Register or Login: Password: Athens/Institution Login Quick Search: within This Journal All Journals All Full-text Sources Journal of Cystic Fibrosis Bookmark this page as: http://www.sciencedirect.com/science/journal/15691993 Articles in Press Volume 4 Volume 4, Issue 3 , Pages 151-210 (September 2005) Volume 4, Issue 2 , Pages 77-150 (May 2005) Volume 4, Issue 2, Supplement 1 , Pages 1-54 (August 2005) Special Issue on infection and inflammation in Cystic Fibrosis Proceedings of a Symposium Organised In Honour of Han van der Laag Volume 4, Issue 1 , Pages 1-75 (March 2005) Volume 4, Supplement 1 , Pages S1-S143 (2005) Volume 3 Volume 2 Volume 1 Alert me when new Journal Issues are available Add this journal to My Favorite Journals Sample Issue Online More Publication Info Information for Authors The Journal of Cystic Fibrosis is the official Journal of the European Cystic Fibrosis Society ... Elsevier B.V.

42. Startown Haunts Startown NC Features the Trail of Fear. Includes photos of the event, fundraiser, prices, and contest information. Helps support cystic fibrosis Foundation. http://www.startownhaunts.com/

Take a walk through the Startown Haunts Haunted Trail! "We put terror in your face!". Startown's Haunted Trail is scary entertainment and may not be appropriate for small children.

43. Cystic Fibrosis Information Page by a woman with CF. Features links to various information on cystic fibrosis. http://www3.nbnet.nb.ca/normap/CF.htm

Cystic Fibrosis I hope that my site will help you to learn more about CF. More about Norma (Added Sept. 30, 2004) Search my site: Symptoms of CF (Updated May 19, 2005) Stories of how difficult it was for some to get diagnosed with CF (Updated Aug. 30, 2003) If it's not CF, then it could be one of these diseases (Updated July 29, 2005) History of CF (Updated May 19, 2005) (Updated July 14, 2005) Common Misconceptions with CF (Updated Feb. 17, 2005) Effects of CF Respiratory Pseudomonas (Up dated Aug. 24, 2005) Burkholderia cepacia and other Burkholderia species (Updated Aug. 30, 2005) ABPA (Allergic Bronchopulmonary Aspergillosis) (Updated July 14, 2005) Other CF Bugs (Updated Aug. 18, 2005) Sinusitis (Updated Apr. 20, 2005) Polyps (Updated Apr. 7, 2003) Hemoptysis (Updated June 16, 2005) The Impact of Hygiene and Microbiology on CF Patients (Link updated Apr. 29, 2003) Other Lung Complications and Treatments (Updated Aug. 18, 2005) How CF Damages Lungs (Added Jan. 9, 1999) Lung Sounds (Updated Jan. 27, 2005) Asthma (Added Dec. 1, 1998)

44. Index Works to try and prevent cystic fibrosis and improve the quality of life for sufferers. Overview, past and present projects, events and information about cystic fibrosis. http://www.geocities.com/cfgeorgia/

var PUpage="76001073"; var PUprop="geocities"; Charity Foundation "Georgian Cystic Fibrosis Center" English Version Georgian Version TRAINING COURSE FOR GEORGIAN CF DOCTOR CFW has approved the grant application of Dr. Lia Shavladze to have a two week training course at the Institute of the Health of Women and Children, Goteborg University. T he following book represents the collection of methodical references about one of the serious genetic disease of the modern world medicine Cystic Fibrosis given in the educational materials, prepared and published in the different languages by the World Health Organization (WHO), Cystic Fibrosis Worldwide (CFW) and world leading centers of CF download full version) Editor: M.D., Ph.D., D.Sc., Professor Karaman Pagava Worked out: Pediatrician of Cystic Fibrosis Clinic Dr. Lia Shavladze BUI LDING CF CLINIC IN TBILISI, GEORGIA GOAL: Provide CF diseased children and adults currently living in the Republic of Georgia, and those who will be born in the future, access to appropriate clinical care, diagnostics, education, necessary medication and supplements in the treatment of CF.

45. Cystic Fibrosis And, there is a subscription cost. In any case, the cystic fibrosis article cited above will not be available from the Human Biology web site. http://www.people.virginia.edu/~rjh9u/cfsciam.html

Cystic Fibrosis December, 1995 The genetic defects underlying this lethal disease have now been shown to eliminate or hobble a critical channel through which a constituent of salt enters and leaves cells by Michael J. Welsh and Alan E. Smith Notice: Scientific American According to Linda Hertz , permissions and rights manager at Scientific American , the magazine cannot grant electronic rights for copies of their articles. However, it is possible to subscribe to the digital version of Scientific American which has monthly issues from 1993 forward. It is not clear if all articles in each issue are available in digital form. And, there is a subscription cost. In any case, the Cystic Fibrosis article cited above will not be available from the Human Biology web site. Maintained by Robert J. Huskey last updated February 12, 2003.

46. Norma Kennedy Plourde's Web Place cystic fibrosis, Genealogy, Kennedy in particular, and other family lines, Rheumatoid Arthritis, and Lac Baker, New Brunswick. English/Fran§ais. http://personal.nbnet.nb.ca/normap/

This page uses frames, but your browser doesn't support them.

47. Cystic Fibrosis Phenotype cystic fibrosis phenotype. Mucus in lungs secreted to trap dust, particles, bacteria, etc; ciliated cells move the mucus upward toward the mouth. http://www.people.virginia.edu/~rjh9u/cfphen.html

Cystic fibrosis phenotype Mucus in lungs secreted to trap dust, particles, bacteria, etc; ciliated cells move the mucus upward toward the mouth. In CF, the mucus is thicker and is not moved by the ciliated cells but stays in the lungs. Results in persistent cough and recurrent lung infections. Pancreas secretes digestive enzymes into the intestine through a gland. In CF, the gland becomes clogged which causes the formation of cysts and eventually the gland becomes fibrous - thus the name: cystic fibrosis of the pancreas (as described by D. H. Anderson in 1938). The intestine does not receive enough digestive enzymes specific for fats resulting in undernourishment and excess fats in the stool (steatorrhea). Reproductive ducts in males become blocked leading to sterility. Sweat glands secrete salt in order to induce the flow of water to the surface of the skin for purposes of cooling; much of the salt is taken back up by the body. In CF, the salt is not taken back up leaving a salt residue on the skin and a salt deficit in the body. Autosomal recessive inheritance established in 1946.

48. Research Interests Studies of cystic fibrosis gene therapy. From the University of Edinburgh in Scotland. http://www.ed.ac.uk/~pthorpe/research.htm

Research Interests Gene Correction of Cystic Fibrosis mutations (1999-) Cystic Fibrosis Gene Therapy Assays (1997-1999) Type I Restriction and Modification Systems (1990-1996) Cystic Fibrosis and Gene Therapy Cystic Fibrosis (CF) and our Gene Therapy research (including lab. Publications) are briefly summarised as part of the Medical Genetics Cystic Fibrosis group within the Medical Genetics Section . Note this site is still under development. Correction of Cystic Fibrosis Mutations 1999- Click here - our current research is detailed on a separate page Cystic Fibrosis Gene Therapy Assays 1997-1999 At the MRC Human Genetics Unit Edinburgh. My research was involved with developing and utilising a variety of assays to study the efficacy of gene delivery and expression of our Gene Therapy reagents. We used quantitative PCR in situ hybridisation to study gene delivery to the lungs; and epitope tagged versions of CFTR to study protein synthesis and localisation. The aim is to have available an array of assays which enable a thorough analysis of the efficiency of gene therapy reagents in all experimental systems, including potential clinical trials. References;

49. Sarah Yourman A young girl with cystic fibrosis and Diabetes that loves competitive skiing, mogul runs, and gymnastics. http://www.sarahyourman.com/

50. Howard Hughes Medical Institute | Biomedical Research & Science Education (HHMI) Biomedical research, grants. HHMI investigators contributed to the discovery of genes related to diseases such as cystic fibrosis and obesity, and to basic understanding of cell development and communication. Scientists are employed by HHMI and conduct their work at HHMI facilities at leading research institutions nationwide. Web site has extensive news and information on recent research findings. http://www.hhmi.org/

2004 HOLIDAY LECTURES: SCIENCE OF FAT Order Now Now available in DVD and VHS HHMI BULLETIN Spring 2005 Issue Online HHMI INVESTIGATOR David Page Germ Cells and Sex Chromosomes in Mammals HHMI INVESTIGATOR Evan Eichler A New View of Human- Chimpanzee Genome Differences Gaining Ground in the Race Against Antibiotic Resistance September 19, 2005 Researchers in Argentina and Mexico have come up with a new strategy that may help science win the battle against antibiotic resistance. More Learning How SARS Spikes Its Quarry September 16, 2005 HHMI researchers have determined the first detailed molecular images of a piece of the spike-shaped protein that the SARS virus uses to grab host cells and initiate the first stages of infection. More Graduate Program and Group Leader Recruiting Move Forward at Janelia September 14, 2005 HHMI announces that its Janelia Farm Research Campus has established partnerships with the University of Cambridge and the University of Chicago to launch an interdisciplinary graduate program. More Human Brain Is Still Evolving September 09, 2005

51. Cystic Fibrosis cystic fibrosis affects the lungs and makes it hard to breathe. Find out more in this article for kids. http://kidshealth.org/kid/health_problems/heart/cystic_fibrosis.html

KidsHealth Kids Kids' Health Problems 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). 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. At school, Lisa coughs a lot, so she keeps a box of tissues on her desk just in case she coughs up mucus and needs to spit it out. In gym class, she participates in sports but often gets tired easily. At lunchtime, Lisa takes pills to help her digest her food and get all the vitamins she needs, which helps her keep up her strength to deal with cystic fibrosis. What Is CF? Cystic fibrosis (CF) is a disease that causes the body to make thick, sticky mucus (say: myoo -kus). This causes problems in two major areas: the lungs and the digestive system. Healthy lungs produce mucus, which protects the airways and makes it easier to breathe. But for a person with CF, the mucus is thick and sticky and can clog up the lungs. This creates a place where bacteria can easily grow - and bacteria cause infections. And it's not only the lungs that are affected in a person who has cystic fibrosis. Mucus-producing cells line the digestive tract, including the stomach, intestines, liver, and pancreas. The pancreas produces enzymes that help digest food and hormones that help absorb sugar. When thick mucus in the pancreas clogs up the narrow passageways, it can make it difficult for people to digest food and get all the vitamins and nutrients they need.

52. Washington University Physicians Department Of Pediatrics Information on this group of specialists for cystic fibrosis, NICU, growth disorders and other conditions. http://www.wuphysicians.com/pediatrics.shtml

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53. Cystic Fibrosis cystic fibrosis (CF) is a genetic disorder that currently affects more than 30000 American children and young adults. http://kidshealth.org/parent/medical/lungs/cf.html

KidsHealth Parents Medical Problems Cystic fibrosis (CF) is a genetic disorder that particularly affects the lungs and digestive system and makes a child more vulnerable to repeated lung infections. Now, thanks to high-tech medical advances in drug therapy and genetics, children born with CF can look forward to longer and more comfortable lives. In the last 10 years, research into all aspects of CF has helped doctors to understand the illness better and to develop new therapies. In the future, ongoing research may help find a cure. What Is Cystic Fibrosis? Currently affecting more than 30,000 children and young adults in the United States, cystic fibrosis makes children sick by disrupting the normal function of epithelial cells - cells that make up the sweat glands in the skin and that also line passageways inside the lungs, liver, pancreas, and digestive and reproductive systems. In CF, the inherited CF gene directs the body's epithelial cells to produce a defective form of a protein called CFTR (or Cystic Fibrosis Transmembrane Conductance Regulator) found in cells that line the lungs, digestive tract, sweat glands, and genitourinary system. When the CFTR protein is defective, epithelial cells can't regulate the way chloride (part of the salt called sodium chloride) passes across cell membranes. This disrupts the essential balance of salt and water that is needed to maintain a normal thin coating of fluid and mucus inside the lungs, pancreas, and passageways in other organs. The mucus becomes thick, sticky, and hard to move.

54. Journal Of Cystic Fibrosis Official bimonthly publication of the European cystic fibrosis Society, devoted to promoting the research and treatment of this disease. Free abstracts available. http://www.elsevier.com/wps/find/journaldescription.cws_home/622283/description#

Home Site map Regional Sites Advanced Product Search ... Journal of Cystic Fibrosis Journal information Product description Editorial board Audience For advertising and sponsorships For Authors Guide for authors Online Submission Subscription information Bibliographic and ordering information Conditions of sale Dispatch dates Journal related information Most downloaded articles Other journals in same subject area About Elsevier Select your view JOURNAL OF CYSTIC FIBROSIS The Official Journal of the European Cystic Fibrosis Society Editor-in-Chief: H. G. M. Heijerman See editorial board for all editors information Description The Journal of Cystic Fibrosis is the official journal of the European Cystic Fibrosis Society . The journal is devoted to promoting the research and treatment of cystic fibrosis. To this end the journal publishes original scientific articles, editorials, case reports, short communications and other information relevant to cystic fibrosis. The journal also publishes news and articles concerning the activities and policies of the ECFS as well as those of other societies related the ECFS. ISSN: 1569-1993 Imprint: ELSEVIER Commenced publication 2002 Subscription for the year 2006, Volume 5, 4 issues

55. Cystic-L - Cystic Fibrosis Info & Support cystic fibrosis information and support, including a vibrant online community, via email, a Handbook of information and resources, photos of CFers, http://www.cystic-l.org/

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

56. Stichting Fibrose Kinderen Op Kamp De stichting Fibrose Kinderen Op Kamp is een uit particulier initiatief voortgekomen stichting, met als doelstelling vakantiekampen te organiseren voor kinderen en jongeren met cystic fibrosis (CF). http://www.stichtingfok.nl/

57. Cystic Fibrosis: What Is It? Your Genes, Your Health, DNA Learning Center s multimedia guide to genetic, inherited disorders cystic fibrosis, autosomal recessive, mutation, http://www.ygyh.org/cf/whatisit.htm

Concept 1 : Children resemble their parents. Learn how Mendel worked out inheritance in pea plants. Concept 10 : Chromosomes carry genes. Find out how genes are arranged on chromosomes. Concept 27 : Mutations are changes in genetic information. Find out how mutations affect gene expression.

58. Ansleysangelsatwork Short story of Ansley who suffers from cystic fibrosis; CF for short, Cerebral Palsy, cortical blindness, brain damage, epilepsy and diabetes, and Protein C deficiency. http://hometown.aol.com/ansleysangels/index.html

htmlAdWH('93212816', '728', '90'); Main My First Home Page Ansley's Angel's At Work Revised 12/13/2004 Midi music and background is from Ansley's favorite videos of "VeggieTales" The "VeggieTales" Corp. has donated several video tapes to be played for Ansley, Thank you "VeggieTales"! Note Updated information near the bottom of page, before pictures You can also go to Ansleys "care Page" for up todate medical events, it requires you to register, but it is simple, go to, Ansley's Medical Update Hi my name is Ansley and I suffer from a Genetic Disorder called Cystic Fibrosis...CF for short...I also have Cerebral Palsy, cortical blindness, brain damage, epilepsy and diabetes, Protein C deficiency....I am now 10 yrs old .....My family has always been here for me and I could not face my life without them...All I have to do is look around and I can see so many people who care about me and my family.. I would love to tell you the story about MY ANGELS, if you would care to hear about them. This year we again will be having another golf Tournament it will be held on September 26 ,2005 at Beautiful PineIsle Golf Resort on Lake Lanier at Buford, Georgia. This course in great shape, and offers a challenge to all players, the course management are ready for us and we look forward to another great year......as always Thank You for your support of Ansley's Needs. This will be our 10 Golf Tournament reserve your place today! You can get information at

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

var monthList = new Array('January', 'February', 'March', 'April', 'May', 'June', 'July', 'August', 'September', 'October', 'November', 'December'); Latest information on Cystic Fibrosis, Services offered by Cystic Fibrosis Victoria, CF chat room and forum, free 65 Roses Magazine, CF shop, fundraising events.

60. SciClone Pharmaceuticals: Welcome Develops and markets products targeted for treatment of cancer and diseases such as hepatitis B and C, cystic fibrosis and immune system disorders. Based in San Mateo, California. (Nasdaq SCLN) http://www.sciclone.com/

Contact Us Sitemap document.write(navOptions[1]); for the treatment of hepatitis C, hepatitis B and certain cancers. SciClone Pharmaceuticals to Present at UBS Global Life Sciences Conference SciClone Reports Second Quarter 2005 Results Most carriers contracted the hepatitis C virus (HCV) before blood screening for the virus began in 1990. Once infected, 20 years can pass before life-threatening complications arise. Unfortunately, nearly half of HCV patients fail current therapy. SciClone is evaluating ZADAXIN in two phase 3 trials, aiming to meet the growing need for a cure for HCV. To learn more More about ZADAXIN ZADAXIN clinical trials Notes Regarding Forward-Looking Statements Site design by Formative

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