141. Hot Dog Safari Details on annual cystic fibrosis research fundraising event at Suffolks Downs. http://www.hotdogsafari.org/

Presented Eddie Andelman's Annual Hot Dog Safari We want to thank everyone who helped make this event another great sucsess. Click here to view video clips from last year's event click on the DVD to view the documentary

142. Cystic Fibrosis International Medical A-Z Directory Cellscience is the A to Z biomedical information directory covering AIDS HIV Cancer - cystic fibrosis - Diabetes and Nervous Disorders. cystic fibrosis. http://cellscience.com/CFmain.html

Cystic Fibrosis rating for web sites is intended to serve only as an indication of the design quality, clarity, presentation and style of the URL, and is in no way intended as a judgement of the quality of services or information provided. To have a site listed is itself an indication that the site is of general interest - (Guide: NR Not rated, strong, good, excellent) Date page was last modified

143. CysticFibrosis.com Internet community for cystic fibrosis patients, families and loved ones. Information on clinical trials, gene therapy, testing, associations, research and events. http://cysticfibrosis.com/

Home CF Centers Associations Clinical Trials Gene Therapy ... New Design! Welcome to the newly designed CysticFibrosis.com website! comment on our forum... Through the eyes of CF I have learned through the years, that having insight and foresight are two valuable tools to have while surviving an illness. read more... Proper nutrition is vital I have learned through the years, that having insight and foresight are two valuable tools to have while surviving an illness. read more... Cystic Fibrosis Information CF is a genetic disorder that affects the respiratory, digestive and reproductive systems. Frequently Asked Questions While there are so many questions that are asked, some are left unanswered. We've got some answers to your FAQs! Just for kids! In terms that they can understand! Learn important information about daily living nutrition stories games ... snacks , and much more... CysticFibrosis.com latest Forum topics Adults - The Vest Families - babies and coughing ... Join our forums, it's compltely free! You may also post anonymously as well!

144. Cystic Fibrosis of human genes and disorders Information Fact sheet from the National Heart, Lung and Blood Institute, NIH The cystic fibrosis foundation information and links. http://www.ncbi.nlm.nih.gov/disease/CF.html

This Genes and Disease page has been moved to: Please update your bookmarks. If you are not automatically transported to the new page after 15 seconds, click on this link Genome View CFTR on chromosome 7 Databases PubMed the literature LocusLink collection of gene-related information OMIM catalog of human genes and disorders Information Fact sheet from the National Heart, Lung and Blood Institute, NIH The cystic fibrosis foundation information and links CYSTIC FIBROSIS (CF) is the most common fatal genetic disease in the US today. It causes the body to produce a thick, sticky mucus that clogs the lungs, leading to infection, and blocks the pancreas, stopping digestive enzymes from reaching the intestines where they are required to digest food. CF is caused by a defective gene, which codes for a sodium and chloride (salt) transporter found on the surface of the epithelial cells that line the lungs and other organs. Several hundred mutations have been found in this gene, all of which result in defective transport of sodium and chloride by epithelial cells. The severity of the disease symptoms of CF is directly related to the characteristic effects of the particular mutation(s) that have been inherited by the sufferer. CF research has accelerated sharply since the discovery of CFTR in 1989. In 1990, scientists successfully cloned the normal gene and added it to CF cells in the laboratory, which corrected the defective sodium chloride transport mechanism. This technique - gene therapy - was then tried on a limited number of CF patients. However this treatment may not be as successful as originally hoped. Further research will be required before gene therapy, and other experimental treatments, prove useful in combating CF.

145. Wescor Inc. Manufactures osmometers, slide stainers, cytocentrifuges, dairy mastitis detection systems, and cystic fibrosis diagnosis equipment. http://www.wescor.com/

About Wescor Employment at Wescor How to Contact Wescor Sweat Testing Instruments About Wescor Employment at Wescor How to Contact Wescor Sweat Testing Instruments ... Weather and Soil

146. Welcome To Genevieve's Cystic Fibrosis Site About a personal journey living with this disease, and alternative therapies used, besides antibiotics. http://www.angelfire.com/ok4/cfgen

var cm_role = "live" var cm_host = "angelfire.lycos.com" var cm_taxid = "/memberembedded" Welcome to Genevieve's Cystic Fibrosis Website. The red rose has been adopted as the universal sign for Cystic Fibrosis. Apparently a young child struggled to say the name, and said "65 Roses". In Australia, a week in October is dedicated to CF week - to help raise money for a cure. So if you see people selling Red Roses, please help our cause. My name is Genevieve. I was born in 1975, and I have a disease called Cystic Fibrosis. In this website, I talk about my personal story with CF, and alternative therapies I have used besides antibiotics. I will constantly update this site with new topics, so please make sure you come back to visit. Cystic Fibrosis is the most common life - threatening condition affecting Australian children. Today with earlier diagnosis, better understanding of the condition and better treatment of the disease, more and more children are reaching adulthood. As CF patients are living longer and healthier lives, new issues develop, such as marriage, being independent, family planning and financial concerns. With such a growing awareness of the disease, these important things and more are being addressed. FOR MORE INFORMATION ABOUT CYSTIC FIBROSIS AND FUND RAISING ACTIVITIES, PLEASE VISIT THE VICTORIAN CYSTIC FIBROSIS WEBSITE.

147. CYSTIC FIBROSIS FOR KIDS This site is made by acenl webdesign the netherlands for children with cystic fibrosis. - - - Welcome to cystic fibrosis for KIDS !!! ). http://members.tripod.com/~jtatton/

var cm_role = "live" var cm_host = "tripod.lycos.com" var cm_taxid = "/memberembedded" 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. Site updated 29-01-2004 IF YOU USE THIS WEB SITE, YOU AGREE TO GIVE UP ANY LEGAL RIGHT YOU MIGHT HAVE TO SUE THE OWNER AND OTHER USERS FOR PERSONAL DAMAGES THAT MAY OCCUR THROUGH ITS USE. THE OWNER PROVIDES THIS WEB SITE AS A FREE SERVICE, AND ASSUMES NO LIABILITY FROM ITS USE.

148. Division Of Genetics, URMC Featured is information on laboratory testing, genetic susceptibility to cancer, cystic fibrosis, and sickle cell, thalassemia and other hemoglobinopathies. In addition there are links to counseling services, the graduate program, the Sickle Cell Clinic, newsletters, and list of staff. http://www.urmc.rochester.edu/Genetics/

Home Services Counseling Services Sickle Cell Clinic Newsletters OncoGene News Sickle Selections Staff Department of Medicine The Division of Genetics offers information on: Genetic Susceptibility to Cancer Sickle Cell, Thalassemia and other Hemoglobinopathies Breast Cancer Recommendations Brochure* A Patient's Perspective Colon Cancer Brochure* Recommendations Brochures/Fact Sheets Our Role in Newborn Screening* ... Brochure* *These files are available as Adobe Acrobat Reader 3.0 files - online versions that look just like the originals. The Adobe Acrobat Reader software is freely available for you to download and use from Adobe's software site. Comments/Suggestions to: Mary_True@urmc.rochester.edu . For questions or suggestions concerning the content of these pages, contact the URMC Webmaster

149. Bronchiectasis In Cystic Fibrosis Bronchiectasis in cystic fibrosis. Jeanne S Chow, MD Bradley Snyder, MD Andetta Hunsaker, MD. Diagnosis. Bronchiectasis resulting from cystic fibrosis. Discussion. http://brighamrad.harvard.edu/Cases/bwh/hcache/211/full.html

Bronchiectasis in Cystic Fibrosis Jeanne S Chow, MD Bradley Snyder, MD Andetta Hunsaker, MD February 12, 1997 Presentation A 37-year-old man presented with chronic cough and worsening dyspnea. Imaging Findings Plain radiographs, PA and lateral views CT of the chest (without intravenous contrast) Computed tomographs (CT) and plain radiographs of the chest demonstrate thickened bronchial walls. In addition, CT images show tubular dilated central bronchi (without tapering) ( arrows ) and mosaic oligemia ( arrows ), in which pulmonary segments most affected by bronchiectasis are distinguished from apparently normal lung tissue. Radiographs further demonstrate parallel line shadows (tram-lines) ( arrows ), ring shadows, and hyperexpansion (note flattened hemidiaphragms). Differential Diagnosis Bronchiectasis Etiologies include: cystic fibrosis bronchial wall weakness (eg, Williams-Campbell syndrome) prior infection (eg, childhood pneumonia, measles, pertussis, mycoplasma, and tuberculosis) obstruction (eg, neoplasms, broncholith, foreign body, bronchostenosis or atresia, granulomatous disease) inhalation and aspiration (eg, ammonia, Riley-Day syndrome, gastric aspiration, heroin overdose)

150. Céline Dion Celine Dion lost her niece to CF and has supported the cause since. http://www.celinedion.com/english/journey_celinesupports.html

151. Modern Information Retrieval - Cystic Fibrosis Collection Modern Information Retrieval cystic fibrosis Reference Collection, http://www.sims.berkeley.edu/~hearst/irbook/cfc.html

Modern Information Retrieval Cystic Fibrosis Reference Collection Contents The Cystic Fibrosis Database (CF) consists of 1239 documents published from 1974 to 1979 discussing Cystic Fibrosis Aspects, and a set of 100 queries with the respective relevant documents as answers. The original collection is available in a single gzipped tar file or a zip file both of 1.47Mb, containing 7 document files and 1 query file. The collection is also available in XML format also in a single gzipped tar file or a zip file both of 1.54Mb, including the Document Type Definition (DTD) for the collection and for each query/answer. Document Files Each document includes 11 fields as follows: Paper Number The first two digits give the year of publication, and the rest three digits range from 1 to the number of docs published that yea Record Number serial id number varying from 1 to 1,239. Medline Acession Number CF is a subset of the MEDLINE database. Author(s) Title Source Bibliographic citation of source. Major Subjects The Medical Subject Headings (MeSH) and subheadings representing the major subjects of the document. The Medical Subject Headings are shown in capital letters and have been assigned by expert indexers. The two-letter symbols are subject subheadings, also assigned manually from a controlled vocabulary (see the MeSH vocabulary published by the National Library of Medicine).

152. Canadian Cystic Fibrosis Foundation - Ottawa Chapter Volunteer organization to aid afflicted individuals, families and care givers. Profile, events and resources information. http://www.ccffottawa.org/

153. If You Ask James About Cystic Fibrosis cystic fibrosis, CF links, cystic fibrosis information including personal experience with CF, treatments, medications, complications, coping, support groups http://www.ajcf.com/

If You Ask James About Cystic Fibrosis preload("twe44152A","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/whatiscf.jpg"); preload("twe44152B","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/whatiscf.jpg"); preload("twe44153A","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/cflinks.jpg"); preload("twe44153B","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/cflinks.jpg"); preload("twe44154A","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/kidsparents.jpg"); preload("twe44154B","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/kidsparents.jpg"); preload("twe44155A","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/treatment.jpg"); preload("twe44155B","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/treatment.jpg"); ... preload("twe441517A","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/legal.jpg"); preload("twe441517B","http://azcowboy88.tripod.com//sitebuildercontent/sitebuilderpictures/legal.jpg"); Cystic Fibrosis,CF links,diagnosis of cystic fibrosis,CF treatments,CF medications,cystic fibrosis foundations,cystic fibrosis awareness,complications of CF,symptoms of cystic fibrosis,causes of cystic fibrosis,cystic fibrosis information,Pseudomonas,Burkholderia cepacia,Pseudomonas aeruginosa,respiratory treatment,chest physiotherapy,cpt,digestive enzymes,mucus,sputum,mal absorption,chronic lung infections,antibiotics,James,James Binegar

154. Cystic Fibrosis Site for those wanting to learn about end stage. Not for someone whose child has been recently diagnosed. By a woman waiting for a lung transplant. http://members.aol.com/JAW060664/html/cf.html

Cystic Fibrosis ... There are many sources of info for cf on the internet. Read my links page and you will find several! This page is for those who wish to know about end stage cf. I'm hoping to get listed for a lung transplant I'm truly very optimistic! However, this page is not intended for someone whose child has been recently diagnosed. I have had a wonderful life. (and it's not not too damn bad now! hahahhaah!) Cystic fibrosis basically the gene defect is too much saltthickens your mucusclogs up all your organsand eventually destroys your lungs. Also affects and can be equally destructiveto the liver, pancreas etc. The complications are innumerable and diversefor more detailcheck my links I have always known I had cf. It is my first memory. I was sitting on my dad's lap, I guess I was about 3 or 4.He said, "you have cystic fibrosis ." Only I thought he said,"you have 65 broses." So I asked him how many he had! I was quite healthy and had a completely normal childhood. I didn't start going into the hospital for the regular "tune up" (two week stay in hospital for i.v. meds) until I was 21 years old. I went to work for the Cincinnati Police Department where I remain as a Police Dispatcher. I am on extended leave awaitinghopefullya lung transplant .

155. Esmerel's Collection Of Cystic Fibrosis Resources cystic fibrosis Resources. (Courtesy Resources. This page is dedicated to cystic fibrosis resources. This list is growing constantly. http://www.esmerel.org/specific/cystic.htm

Cystic Fibrosis Resources (Courtesy of Esmerel: Home of Unicorn Quest : The Kids' Typing Tutor Game for One or Two Hands ) Welcome to another part of Esmerel's Collection of Disability Resources. This page is dedicated to cystic fibrosis resources. This list is growing constantly. If you know of any other resources or have suggestions, please email Heather. Cystic Fibrosis.com Cystic Fibrosis Cystic Fibrosis 101 ... Norma Kennedy Plourde CF Page This site has many links and various information for the average person with cystic fibrosis. Sarah's Cystic Fibrosis Page Web Creations Cystic Fibrosis Page Back to the Disabled Directory This page is maintained by Heather

156. Hanissian Clinic, P.C. A clinic providing allergy, asthma, immunology, rheumatology, and cystic fibrosis care for children and adults by Drs. Gregory and Aram Hanissian. http://www.hanissianclinic.salu.net

157. The Cystic Fibrosis Web Page Of The Niagara Cystic Fibrosis Chapter Canada Information from the Niagara cystic fibrosis chapter in Canada. http://www.iaw.on.ca/~meb/

NIAGARA CYSTIC FIBROSIS CHAPTER Hello !! My name is Mary-Ellen Benn. I am the president of the Niagara Cystic Fibrosis Chapter. The Niagara Cystic Fibrosis Chapter is a small group of parents and concerned citizens working very hard to raise funds for reasearch to find a cure or control for Cystic Fibrosis. I am available to answer any questions or concerns you may have about Cystic Fibrosis. I work mostly afternoons so the best time to get in touch with me is in the morning. If you subscribe to ICQ and I am on line you can contact me directly my ICQ # is 8134001 My favorite places on the web CANADIAN CYSTIC FIBROSIS FOUNDATION CYSTIC-L COMMUNITY PAGE ICQ CF CHAT ROOM INFORMATION PAGE Mary, Mike and Rob's Personal ICQ information Page ... The Cystic Fibrosis Chatroom information Page ICQ based. Together we will make CF stand for Cure Found !!!! If Your Not Living On The Edge Your Taking Up To Much Room !!! If you have comments or suggestions email me at This page is Designed by Mary-Ellen Benn Maintenance by Acctech the Netherlands Webdesign and Webdevelopment.

158. Peter Rabbit Has Cystic Fibrosis JOHNNY RABBIT HAS cystic fibrosis. cystic fibrosis is a disease. Click here if you don t know much about it. Version française. A http://perso.wanadoo.fr/jielge/cysticrab.htm

JOHNNY RABBIT HAS CYSTIC FIBROSIS Cystic fibrosis is a disease. Click here if you don't know much about it. Version française A picture story to tell the life of affected children : Chapter 1: Screening Chapter 2: The treatment Chapter 3: Stranges thinks Chapter 4: A new story Information, comments

159. Gateway Chapter, Cystic Fibrosis Foundation (St. Louis) Contact and service information. http://www.tenholder.net/gatewaycff/

Click the CD Player to the left to hear a 60 second sample of "One Heart at a Time" , a special song written exclusively for the Cystic Fibrosis Foundation. If you like the sound, click the CD Jacket on the right to read more about this CD and how you can add it to your collection. Learn more about the Great Strides Walk to Cure CF . . . click the button below this banner. About the Cystic Fibrosis Foundation The Cystic Fibrosis Foundation (CFF) was established in 1955 to raise money 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 CFF puts funds to work as efficiently as possible; 90% of all money raised goes to CF research. The Gateway Chapter of the Cystic Fibrosis Foundation (Gateway CFF) raises money in the St. Louis, Missouri Metropolitan area, various locations throughout the state of Missouri, and St. Louis' neighboring counties in Western Illinois. Money raised by the Cystic Fibrosis Foundation supports: A network of multidisciplinary research and gene therapy centers at major universities across the United States.

160. Cystic Fibrosis Clinical And Research Center - Children's Hospital And RegionalM Children s Hospital and Regional Medical Center cystic fibrosis Center (Pediatrics) 4800 Sand Point Way NE, 3D2 Phone 206-987-2024 Fax 206-987-2639. http://depts.washington.edu/cfcenter/

Site Under Construction Children's Hospital and Regional Medical Center Cystic Fibrosis Center (Pediatrics) 4800 Sand Point Way NE, 3D-2 Phone: 206-987-2024 Fax: 206-987-2639 University of Washington Cystic Fibrosis Clinic (Adults) Nurse Coordinator: Gwen McDonald, RN (206) 598-8446 Clinic Days/Hours: Mondays 8:30-12:30 Appointments: Rebecca Larson (206) 598-4615 Cystic Fibrosis Research Center - Adult and Pediatric Research Studies: Sharon McNamara, (206) 987-3921 Research Funding: Emily Sasnett, (206) 987-3861 General Information: Molly Andrina, (206) 987-1208 Cystic Fibrosis Therapeutics Development Network Coordinating Center Suites 90, 122 and 228 2611 NE 125th St. Seattle, WA 98125 Phone: 206-527-5725 Fax: 206-527-5767

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