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         Cystic Fibrosis:     more books (100)
  1. Cystic Fibrosis (European Respiratory Monograph) by A. K. Webb & F. A. Ratjen, 2006-04-01
  2. Cystic Fibrosis, Basic and Clinical Research: Proceedings of the 17th Annual Meeting of the European Working Group for Cystic Fibrosis, Copenhagen, (International Congress Series) by Niels Hoiby, 1993-04
  3. Family Nursing: The Case of Cystic Fibrosis by Dorothy A. Whyte, 1994-05
  4. The Official Parent's Sourcebook on Cystic Fibrosis: A Revised and Updated Directory for the Internet Age by ICON Health Publications, 2005-01-26
  5. Cystic Fibrosis: Manual of Diagnosis and Management by Mary C. Goodchild, John A. Dodge, 1985-10
  6. Cystic Fibrosis: Directory of Authors of New Medical and Scientific Reviews With Subject Index by Science & Life Consultants Association S, 1996-05
  7. A Parent's Guide to Cystic Fibrosis (University of Minnesota Guides to Birth and Childhood Disorders) by Burton L. Shapiro, Ralph C. Heussner, 1991-02
  8. Cystic fibrosis: A comprehensive bibliography of the medical literature, 1813-1972 by Douglas S. Holsclaw, 1977-01-01
  9. Cystic Fibrosis (Health Alert) by Ruth Bjorklund, 2008-09
  10. Mucus Secretions and Cystic Fibrosis: Conference on Mucus Secretions and Cystic Fibrosis, Southern Ontario, October 24-27, 1976 (Modern Problems in Paediatrics)
  11. Cystic Fibrosis: New Research
  12. Cystic Fibrosis (Explaining) by Jillian Powell, 2009-02-12
  13. Little Brave Ones: For Children Who Battle Cystic Fibrosis by Carrie Lux, 2006-03-08
  14. Cystic Fibrosis (Lung Biology in Health and Disease)

81. 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.

82. Boogerwoods
Contains a history of the event that benefits cystic fibrosis.
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. PHANIELS CHURCH RD , ROCKWELL / CHINA GROVE NC

83. Cystic Fibrosis Ibuprofen Laboratory
The cystic fibrosis Ibuprofen Laboratory (located at Case Western Reserve University in Cleveland, Ohio) provides ibuprofen analyses and therapeutic
Cystic Fibrosis Ibuprofen Laboratory
Welcome to the Cystic Fibrosis Ibuprofen Laboratory !!!
The old URL for the Cystic Fibrosis Ibuprofen Laboratory ( will soon be changing. The new URL will be 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.

84. Wel Eens Aan Een Longtransplantatie Gedacht?
Een persoonlijke site van een cystic fibrosis pati«nt over longtransplantatie.
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 Yun Hu Berdy van Schijndel Baske van den Hoven

85. 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
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

86. 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.
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.

87. About Recipes For Kids With Cystic Fibrosis
Learn to make these highcalorie recipes, like cheesecake squares, cheesy mashed potatoes, and baked creamy chicken.
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.

88. Cystic Fibrosis
With cystic fibrosis. Pancreas, 3pict.jpg (68738 bytes) Normal pancreas, Pancreas from a cystic fibrosis patient, showing infiltration of fat and
Cystic Fibrosis
Normal With Cystic Fibrosis Pancreas
view 342 KB version

view 67 KB version

view 284 KB version

view 46 KB
version Normal pancreas Pancreas from a cystic fibrosis patient, showing infiltration of fat and fibrotic lesions. Lung
view 229 KB version

view 25 KB version

view 125 KB version

view 22 KB version
Normal lung tissue Lung tissue from a cystic fibrosis patient, showing extensive destruction as a result of obstruction and infection. Examinations Photographs Movies Links ... noJava Home

89. Cystic Fibrosis Carrier Testing: The Decision Is Yours
This booklet was prepared to give you information about cystic fibrosis (CF) cystic fibrosis carrier testing is a laboratory test done on a sample of
T his booklet was prepared to give you information about cystic fibrosis (CF) and CF carrier testing. Carrier testing is being made available to you on a voluntary basis. Testing can be right for some people and not right for others based on many factors. These include your level of risk, your family situation, plans and needs, and your religious and spiritual beliefs. Whether or not you are tested is a personal decision that belongs to you and your baby's father. Before deciding, you should read this booklet so you understand what CF is and what carrier testing is about. On page 9 of this booklet, there is space for you to write down any questions you may have. Whether or not you are tested is a personal decision that belongs to you and your baby's father. If, after reading the booklet, you want to be tested, or simply want to know more about the test, you should tell your health care provider that you are interested in learning more about CF carrier testing. You may also want to check to make certain that the cost of CF testing is covered by your insurance company. What is cystic fibrosis?

90. 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.
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 Download our

91. 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.
Immunotherapy to fight cancer Home page Site Map Contact Us Search Corporate Overview


... 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 : 09.09.2005 (delayed) Eurolist Paris Share Warrants Last: Volume: Change: Nasdaq Share Last: $ 3.40(c) Volume: Change: CAPITAL INCREASE Clinical Trials Job Opportunities French version Webm@ster

92. 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
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

93. Pennsylvania Cystic Fibrosis Inc.
Dedicated to education and information for those interested in CF.
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

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

94. Cochrane Cystic Fibrosis & Genetic Disorders Homepage
Cochrane cystic fibrosis Genetic Disorders Group.
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.

95. 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
Wikimedia needs your help in its 21-day fund drive. See our fundraising page
Over US$220,000 has been donated since the drive began on 19 August. Thank you for your generosity!
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.
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 pneumonia or heart failure.

96. Cystic Fibrosis
Learn about what it is, the causes, what happens to the body, and how to live with it.

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

97. Cystic Fibrosis News
News on cystic fibrosis collected from diverse sources on the web.
Advanced Search Enter ZIP, City or News Search
Cystic Fibrosis News

98. Cystic Fibrosis New Zealand
The cystic fibrosis Association of New Zealand is an incorporated society providing membership for regional groups, businesses and individuals who wish to
General Information Inheritance of Cystic Fibrosis 65 Roses Story Welfare Grants ... Contact Information Cystic Fibrosis Association of New Zealand The Cystic Fibrosis Association is an incorporated society providing membership for regional groups, businesses and individuals who wish to work together in support of people with cystic fibrosis and their families. There are branches in most regions to provide local support. STREET APPEAL SUCCESS Thanks to our great friends at Harveys real Estate, Friday 12th's collection day was FANTASTIC! Final totals will be available within the next few weeks, but in the meantime, thank you to all those who volunteered their time and their energy for this great cause of ours. Our Goal:
The goal of the Association is to ensure increased life expectancy for people with cystic fibrosis and improved quality of life for them and their families; and through research to achieve better control and ultimate cure for the illness. Currently there are funds available for CF Research; applications should be made through Child Health Research (Cure Kids). An application form is available online at

99. 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.

Wellness Center

HHCS Corporate


Cystic Fibrosis

Wellness Center

HHCS Corporate


Cystic Fibrosis
Agency for Healthcare Administration

100. 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.
:: 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

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