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         Cystic Fibrosis:     more books (100)
  1. Mucus Secretions and Cystic Fibrosis: Conference on Mucus Secretions and Cystic Fibrosis, Southern Ontario, October 24-27, 1976 (Modern Problems in Paediatrics)
  2. Volume 2, Cystic Fibrosis--Current Topics by J. A. Dodge, D. J. H. Brock, et all 1995-01-31
  3. Cystic Fibrosis
  4. Inhalation Therapy: Roche and Genentech Symposium European Cystic Fibrosis Conference, Paris, June 1994 (Respiration, Vol 62, Suppl 1) by Ch Koch, 1995-04
  5. Cystic fibrosis: An entry from Thomson Gale's <i>Gale Encyclopedia of Nursing and Allied Health</i> by L. Fleming, Jr., M.D, Dr.P.H. Fallon, 2002
  6. Cystic Fibrosis (Perspectives on Diseases and Disorders)
  7. Learn from cystic fibrosis for other feeding problems: nutritional strategies overlap.(Behavioral Pediatrics): An article from: Pediatric News by Sherry Boschert, 2004-03-01
  8. G542X as a probable Phoenician cystic fibrosis mutation.: An article from: Human Biology by France Loirat, Serge Hazout, et all 1997-06-01
  9. Lung Transplantation for Cystic Fibrosis: Additional Considerations.: An article from: Pediatric Nursing by Sarah Vittone, 2001-01-01
  10. Living With Cystic Fibrosis (Living Well Chronic Conditions) by Susan Heinrichs Gray, 2002-08
  11. Adequate nutrition one of four key Tx tactics for CF infants: impact can be dramatic.(Clinical Rounds)(cystic fibrosis): An article from: Pediatric News by Timothy F. Kirn, 2003-12-01
  12. Guide to Diagnosis and Management of Cystic Fibrosis by Unknown, 1971
  13. Animal Models for Cystic Fibrosis: The Reserpine-Treated Rat
  14. Cystic Fibrosis (Lung Biology in Health and Disease) by Davis, 1993-03-31

81. Copernicus Theraputics - Home
Developing human gene therapy products for cystic fibrosis and hemophilia B and DNA vaccinations. The company creates proprietary PLASmin Complexes which are efficient nonviral vectors and REPLIsome vectors which allow replication of non-viral vectors.
http://www.cgsys.com/index/index.asp
Copernicus Therapeutics, Inc. is a privately-held company developing products for human gene therapy and vaccination. Copernicus was established in 1997 based on technologies discovered at Case Western Reserve University that provide the foundation for the use of DNA as drugs.
Copernicus is not involved in gene discovery or the linkage of genetic defects to disease. Copernicus' business focuses on using its technologies to make and sell gene therapy products to treat, cure or prevent human diseases - products that work.
Copernicus Therapeutics, Inc. presented data at the American Society of Gene Therapy meeting showing that their compacted DNA formulation can effectively transfect non-dividing human cells, solving the problem of restricted access of plasmid DNA to the nucleus. ..read more
Copernicus has developed three technology platforms that provide unique opportunities to develop novel therapeutics. These platforms have separate therapeutic applications but, when combined, can result in synergistic advantages. ..read more
Copernicus' technologies present opportunities for products in many important markets. The Company's delivery technologies solve many of the problems that have hindered gene therapy, with a market projected to be worth $12 billion by 2007.

82. The Cystic Fibrosis (CF) Center At Stanford
cystic fibrosis Center at Stanford research and clinical trials, Pediatric and Adult CF Programs, CF sweat chloride tests, education regarding pulmonary
http://cfcenter.stanford.edu/
Banner Navigatiion Guide Main Page Thank you for visiting The CF Center at Stanford, a site dedicated to Cystic Fibrosis. Since your browser doesn't support frames, you will need to go directly to the main page

83. Boogerwoods
Contains a history of the event that benefits cystic fibrosis.
http://www.boogerwoods.com
THE ORIGINAL ONE AND ONLY !! ................................THE ORIGINAL ONE AND ONLY !! ................................THE ORIGINAL ONE AND ONLY !! ................................THE ORIGINAL ONE AND ONLY !! ................................ Boogerwoods was a BIG hit in the Palestine and Kannapolis Christ mas Parades this year. The Internet's Premiere Halloween Publication PARKING WILL BE LIMITED PLEASE CARPOOL Limited Amount Of Tickets Each Night,, Tickets On Sale At 2:00 PM Each Day And They Sales Out Quick! Tickets Are Sold Each Day On Location Only. No Tickets Sold Online. BOOGERWOODS IS BACK! W ith an all NEW SHOW. Dates- Oct. 27,28,29, and 31st. 2005 , 4 nights only. New scenes are the Drive Thru, Booger Middle School, 3D Room and Vortex, and the Flatbacks are Back. Your favorite scenes like Club Booger, Booger Meat Packing, Twister and others are back also. Information About Boogerwoods Call 704- 855- 7922 PHANIELS CHURCH RD , ROCKWELL / CHINA GROVE NC

84. Cystic Fibrosis News
cystic fibrosis News continually updated from thousands of sources around the net.
http://www.topix.net/health/cystic-fibrosis
Advanced Search Enter ZIP, City or News Search
Cystic Fibrosis News

85. Wel Eens Aan Een Longtransplantatie Gedacht?
Een persoonlijke site van een cystic fibrosis pati«nt over longtransplantatie.
http://www.longtransplantatie.nl/
Donortoewijzing in Nederland Forum longtransplantatie Chatbox longtransplantatie op wachtlijst getransplanteerd getransplanteerd getransplanteerd getransplanteerd overleden Paul van den Elsaker Arian Visser Hans van de Vooren Jeroen Kleijn René Oud Adri Thijssen overleden getransplanteerd getransplanteerd getransplanteerd getransplanteerd getransplanteerd Tessy van Grimbergen Benny de Louw Bjorn den Haan Esmé Geurkink Wout den Boggende Shanna Jager getransplanteerd getransplanteerd getransplanteerd op wachtlijst overleden overleden Robert Stoelenga Patrick Spannenburg Ellen Stoelenga Sandy Roorda Astrid Selhorst Martijn Tunnissen getransplanteerd getransplanteerd overleden getransplanteerd getransplanteerd op wachtlijst Maurice van Opdorp Elvira Luyendijk Lex van Heusden Peggy Landman Frans Zonneveld Twan Martens getransplanteerd getransplanteerd getransplanteerd op wachtlijst getransplanteerd op wachtlijst Yun Hu Berdy van Schijndel Baske van den Hoven

86. Cystic Fibrosis - Doctor S Guide To The Internet
The latest medical news and information for patients or friends/parents of patients diagnosed with cystic fibrosis and cystic fibrosisrelated disorders.
http://www.pslgroup.com/CF.HTM

87. Cystic Fibrosis Ibuprofen Laboratory
The cystic fibrosis Ibuprofen Laboratory (located at Case Western Reserve University in Cleveland, Ohio) provides ibuprofen analyses and therapeutic
http://www.cwru.edu/affil/CFIBUPLAB/cfibuplab.htm
Cystic Fibrosis Ibuprofen Laboratory
Welcome to the Cystic Fibrosis Ibuprofen Laboratory !!!
ATTENTION
The old URL for the Cystic Fibrosis Ibuprofen Laboratory (http://www.cwru.edu/orgs/CFIBUPLAB/cfibuplab.htm) will soon be changing. The new URL will be http://www.cwru.edu/affil/CFIBUPLAB/cfibuplab.htm. You might have been automatically redirected from the old URL to this new URL - however, this redirection will not last indefinitely, so please change your links! Thank you for your patience!
The Cystic Fibrosis Ibuprofen Laboratory provides ibuprofen analyses and therapeutic recommendations to physicians treating cystic fibrosis patients with ibuprofen. WWW (greater than 2.0) browser. General Information about our Lab
How we got started and what we do. For patients
General Information for Patients and Families affected by CF. For Physicians and Healthcare Professionals
Information for physicians and/or healthcare professionals treating patients afflicted with CF. Brief Method Description
How we determine the ibuprofen levels in the patient specimens. Request Test Kit
How to request a test kit.

88. About Recipes For Kids With Cystic Fibrosis
Learn to make these highcalorie recipes, like cheesecake squares, cheesy mashed potatoes, and baked creamy chicken.
http://www.kidshealth.org/kid/recipes/cf_recipes/about_cf_recipes.html
KidsHealth Kids Recipes Recipes for Kids With Cystic Fibrosis
These high-calorie recipes are especially for kids with cystic fibrosis (CF). Kids with CF may need additional calories to meet their nutritional needs . Check out these delicious recipes: Alfredo Pesto Pasta
Bacon and Cheddar Cheese Quiche

Bacon Cheeseburger

Bacon Mushroom Chicken
... Editorial Policy
Note: All information on KidsHealth is for educational purposes only. For specific medical advice, diagnoses, and treatment, consult your doctor.

89. Cystic Fibrosis "I.Q." Test
The following statements test what you know about cystic fibrosis. Fill out the test by choosing true or cystic fibrosis (CF) is a hereditary disease.
http://www.yourlunghealth.org/staying_healthy/iq_tests/cystic_fibrosis_iq1.cfm
The following statements test what you know about Cystic Fibrosis. Fill out the test by choosing true or false, then press the submit button.
True False Cystic fibrosis (CF) is a hereditary disease. CF is more common in white children than in children of other races. As many as 30% of Americans of European descent carry the gene which is responsible for CF. The lungs are the only organs affected by CF. A person with CF may have difficulty keeping off excess weight. Treatment of CF has not changed much in the past twenty-five years. The gene responsible for CF has been identified. There is no way to tell if a newborn will get CF. Gene therapy is a standardized treatment for CF. People with CF require treatment only when they have an attack.

90. Genome.gov | Learning About Cystic Fibrosis
Answers to frequently asked questions about cystic fibrosis, published by the National Human Genome Research Institute.
http://www.genome.gov/10001213
triggerParms["cpp_5"] = "Referer:"+ cppUrlPatch (""); // Optional Home About NHGRI Newsroom Staff ... Specific Genetic Disorders Learning About Cystic Fibrosis
Learning About Cystic Fibrosis
What do we know about heredity and cystic fibrosis? Is there a test for the cystic fibrosis gene? NHGRI Clinical Research on Cystic Fibrosis Additional Resources for Cystic Fibrosis Information
What do we know about heredity and cystic fibrosis?
Cystic fibrosis (CF) is the most common, fatal genetic disease in the United States. About 30,000 people in the United States have the disease. CF causes the body to produce thick, sticky mucus that clogs the lungs, leads to infection, and blocks the pancreas, which stops digestive enzymes from reaching the intestine where they are required in order to digest food. Cystic Fibrosis: A Single Gene Disease Mutations in a single gene - the Cystic Fibrosis Transmembrane Regulator (CFTR) gene - causes CF. The gene was discovered in 1989. Since then, more than 900 mutations of this single gene have been identified. In normal cells, the CFTR protein acts as a channel that allows cells to release chloride and other ions. But in people with CF, this protein is defective and the cells do not release the chloride. The result is an improper salt balance in the cells and thick, sticky mucus. Researchers are focusing on ways to cure CF by correcting the defective gene, or correcting the defective protein.

91. Welcome To Cystic Fibrosis Western Australia
Includes a calendar of events, information for people with CF who travel to Australia from other countries (what their healthcare entitlements are), pointers for teachers of children with CF, and a list of services and support.
http://www.cysticfibrosiswa.org
Cystic Fibrosis WA website is sponsored in memory of David Goldberg
Welcome to Cystic Fibrosis Western Australia
Survey Results Member Needs Analysis Research Findings June 2005 - large file, please be patient!
View Results
This presentation requires Adobe Reader 5.0 or better. Upgrade your version here Australian and New Zealand Cystic Fibrosis Conference August 20-23 2005
More info
The Niche
11 Aberdare Rd (Cnr Hospital Ave),
Nedlands WA 6009
PO Box 959, Nedlands WA 6909 Ph: (08) 9346 7333
Fax: 9346 7344
Freecall: 1800 678 766
Order Capel Vales wines and support CFWA
Limited copies of 2005/06 Entertainment Book still available Last Update: Tuesday, August 16th 2005
L.J. Hooker Supporting Cystic Fibrosis Australia All queries to info@cysticfibrosiswa.org Download our

92. Transgene
Gene therapy company based in France is developing products for cancer and cystic fibrosis. Vector platforms include adenovirus, retrovirus, vaccinia virus, cellular and synthetic vectors.
http://www.transgene.fr/us/
Immunotherapy to fight cancer Home page Site Map Contact Us Search Corporate Overview
History

Products

Locations
... News Company Profile Transgene is a biopharmaceutical company dedicated to the discovery and development of therapeutic vaccines and immunotherapy products for the treatment of cancer and infectious diseases.
Corporate presentation (PDF June 2005)
Product Pipeline MVA-MUC1-IL2 : Phase II MVA-HPV-IL2 : Phase II Phase I/II MVA-HCV : Preclinical Ad-IL2 (suspended): Phase I/II MVA-FCU1 (suspended): Preclinical
Production Since 1995, Transgene operates its own multi-use, multi-product manufacturing
News Press Releases
August 3, 2005
Transgene announces first half 2005 financial results ...
July 21, 2005 July 11, 2005 Stock Quotes Date : 09.20.2005 (delayed) Eurolist Paris Share Warrants Last: Volume: Change: Nasdaq Share Last: $ 2.81(c) Volume: Change: CAPITAL INCREASE Clinical Trials Job Opportunities French version Webm@ster

93. Genome.gov | Learning About Cystic Fibrosis
cystic fibrosis Carrier Testing The Decision is YoursThis booklet was prepared to give you information about cystic fibrosis (CF) cystic fibrosis carrier testing is a laboratory test done on a sample of
http://www.genome.gov/page.cfm?pageID=10001213

94. Pennsylvania Cystic Fibrosis Inc.
Dedicated to education and information for those interested in CF.
http://www.pacfi.org/
Home of the million dollar bear campaign
Flying And Dreaming With........Burke P Bear

"Million Dollar Bear" Campaign and "Burke's Tour" FAQ

What Is Cystic Fibrosis

Wonderful Legacy
...
update.

Burke P. Bear was proclaimed "The Pennsylvania Ambassador for Love, Peace, Having Fun, and Curing Cystic Fibrosis" in a unanimous 199-0 vote by the PA House of Representatives in June, 1999. "Burke's Tour" is taking the traveling ambassador through each state and several world countries. So far he has visited 35 states and more than a dozen world countries where he spreads his ambassador's messge: To love each other, to live peacefully, to have fun, and to help cure CF.
For more information; please contact PACFI at 1-800-900-2790 by fax at (570) 374-2612 email

95. ACOG Education Pamphlet -- Cystic Fibrosis Testing: What Happens If Both My Part
What is the chance that my baby will have cystic fibrosis? What are the health needs of children with cystic fibrosis? The digestive problems usually
http://www.acog.org/from_home/wellness/cf002.htm
N ot long ago, you and your partner took a carrier test for cystic fibrosis (CF). You have been given this booklet because the results of that test revealed that both you and your partner are carriers of the changed CF gene (CF carriers). The purpose of this booklet is to explain to you the meaning of your test results and what steps you can take next. In each pregnancy the two of you have together, the baby will have a 1-in-4 chance of having CF. It is completely normal at a time like this to feel distressed and confused. We hope that after reading this booklet, you will feel somewhat reassured and have a much better understanding of your situation. After you read this booklet, it will be helpful for you to speak with your health care provider about the next steps you want to take. You might want to plan to bring your partner to this visit or bring any other people with whom you usually share important decisions. They might want to read this booklet as well. What do my test results mean? The test results mean that you and your partner are both carriers of the changed CF gene. This does not have any impact on your health. However, it means that your developing baby

96. Cochrane Cystic Fibrosis & Genetic Disorders Homepage
Cochrane cystic fibrosis Genetic Disorders Group.
http://www.liv.ac.uk/cfgd/
Cystic Fibrosis . Phenylketonuria . Sickle Cell . Haemophilia . Other Genetic Disorders Activities of the Group are co-ordinated by its Editorial Base, located within the Department of Child Health, University of Liverpool, United Kingdom. We very much welcome interest from new consumers, referees and potential reviewers. A list of our priority review titles can be accessed by clicking here . Further information can be found here or by contacting the group The Group has 52 reviews, 11 protocols and 6 titles published on Issue 3, 2005 of The Cochrane Library . The production of these reviews involves a network of 250 authors, consumers and referees throughout the world. Last reviewed 17 June 2002.

97. Cystic Fibrosis
Learn about what it is, the causes, what happens to the body, and how to live with it.
http://www.kidshealth.org/teen/diseases_conditions/digestive/cystic_fibrosis.htm

KidsHealth
Teens Digestive System
When the students in Mrs. Hill's eighth-grade algebra class heard that the new guy joining their class had cystic fibrosis, they weren't sure what to expect. They wondered if he would look pale and sick or if he would need help carrying his books or getting around. But when Alex finally arrived, everyone was surprised. Although Alex coughed sometimes and he had to take medicine and eat several times a day, he looked healthy and participated in sports, played guitar, and enjoyed camping. What Is Cystic Fibrosis?
Cystic fibrosis (CF) is an inherited disease that causes the body to produce mucus that's extremely thick and sticky. The mucus in people with CF is thicker than normal because CF affects cells in the epithelium (pronounced: eh-puh- thee -lee-um), the layer of cells that lines the passages in the body's organs. In a person who does not have CF, the epithelial cells produce a thin, watery mucus that acts like a lubricant and helps protect the body's tissues. In a person with CF, however, the thicker mucus doesn't move as easily. This thick, sticky mucus clogs passages in many of the body's organs. The two organs that are most affected are the lungs and pancreas , where the thick mucus causes breathing and digestive problems. The thicker mucus has trouble moving out of the lungs, so bacteria can remain and cause infections. The thick mucus can also be found in the pancreas

98. Cystic Fibrosis - Wikipedia, The Free Encyclopedia
cystic fibrosis (CF) was first described as a disease in the late 1930s. Since cystic fibrosis is recessive, both copies of the gene have to be CF genes
http://en.wikipedia.org/wiki/Cystic_fibrosis
Cystic fibrosis
From Wikipedia, the free encyclopedia.
Cystic fibrosis
Cystic fibrosis CF
), also called mucoviscidosis , is an autosomal recessive hereditary disease of the exocrine glands . It affects the lungs sweat glands and the digestive system . It causes chronic respiratory and digestive problems.
Contents
edit
Symptoms
The symptoms of CF usually develop during early childhood. Both lungs and pancreas produce abnormally viscous mucus . This mucus begins to build up and starts to clog the opening to the pancreas and the lungs. The mucus in the lungs can become a growth medium for bacteria, resulting in chronic respiratory infections and eventual permanent damage to the lung tissue. A chronic and loose sounding cough is common in people with CF. These thick secretions also obstruct the pancreas, preventing digestive enzymes from reaching the intestines to help break down and absorb food. Frequent and foul smelling stools are often an early sign of CF along with fatty oil that is visible in the stool. This can compromise growth and overall nutrition if proper treatment to aid digestion is not utilized early in life. As lung function deteriorates, CF patients can develop pulmonary hypertension and eventually cor pulmonale . Death usually occurs from severe infection

99. The Cystic Fibrosis Association Of Ireland
Welcome to the cystic fibrosis Association of Ireland.Working with CF patients and their families to promote health, education and a better way of life.
http://www.cfireland.ie/
:: CLICK HERE to enter the CF Ireland web site :: Web site best viewed at 800 x 600 pixels, True Color (32 Bit), version 4+ java enabled browsers. Optimised for Microsoft Internet Explorer 5+
Site developed with Lucasart and the CF Association of Ireland

100. Welcome To The HHCS Health Group Of Companies
A fullservice pharmacy, disease management and medical management company encompassing the cystic fibrosis pharmacy, medi-paws pet pharmacy, and a vitamin and supplements pharmacy program for homeopathic medicine.
http://hhcs.com/

Wellness Center

HHCS Corporate

Center

Cystic Fibrosis

Wellness Center

HHCS Corporate

Center

Cystic Fibrosis
...
Agency for Healthcare Administration

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