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         Cystic Fibrosis:     more books (100)
  1. Genetic Disorders Sourcebook: Basic Consumer Health Information About Hereditary Diseases and Disorders, Including Cystic Fibrosis, Down Syndrome, Hemophilia, ... Disease (Health Reference Series)
  2. Derm diagnosis.(Clinical Rounds)(rash caused by malnutrition in an infant with cystic fibrosis): An article from: Family Practice News by Timothy F. Kirn, 2003-09-01
  3. Cystic Fibrosis: Nutri-tional and Intestinal Disorders by Ross W. Shepherd, Geoffrey J. Cleghorn, 1989-09-30
  4. Cystic Fibrosis
  5. Fluid and Electrolyte Abnormalities in Exocrine Glands in Cystic Fibrosis
  6. Everything You Need to Know About Cystic Fibrosis (Need to Know Library) by Justin Lee, 2001-10
  7. Cystic Fibrosis: Horizons (A Wiley Medical publication) by David Lawson, 1984-05-23
  8. Cystic Fibrosis by Alvin; Silverstein, Robert; Silverstein, Virginia Silverstein, 1993
  9. Cystic Fibrosis (Genetic Diseases) by Maxine Rosaler, 2006-08-31
  10. Cystic Fibrosis (Molecular Medicine)
  11. Cystic Fibrosis (Perspectives on Disease and Illness) by Retold by:, 2001-09-01
  12. Treatment of the Hospitalized Cystic Fibrosis Patient (Lung Biology in Health and Disease, vol. 109)
  13. Progress In Cystic Fibrosis Research
  14. Psychosocial Aspects of Cystic Fibrosis; A Model for Chronic Lung Disease. by Paul R. Patterson, 1973-06

41. ScienceDirect - Journal Of Cystic Fibrosis - List Of Issues
cystic fibrosis WorldwideInternational Association of cystic fibrosis Adults web site and International cystic fibrosis Mucoviscidosis Association.
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:
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.
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.
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:

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

47. Cystic Fibrosis Molecular Biology
cystic fibrosis gene to product first nucleotide binding function (NBF1) domain of the cystic fibrosis transmembrane conductance regulation protein.
Cystic fibrosis: gene to product
Graphic taken (in part) from Human Genetics: Concepts and Applications by Ricki Lewis (1994), Wm. C. Brown
The most frequently occurring mutation, delta-F508, is a single amino acid deletion in exon 10 which codes for a portion of the first nucleotide binding function (NBF-1) domain of the cystic fibrosis transmembrane conductance regulation protein. Although the mutant protein is produced since it is only missing one amino acid, it seems to be identified as non-functional and does not undergo the usual final modifications within the endoplasmic reticulum. Instead, the mutant protein is degraded. A list of other CF mutations is available
Links to information on CF

This document maintained by Robert J. Huskey Last updated on August 24, 1995.

48. Research Interests
Studies of cystic fibrosis gene therapy. From the University of Edinburgh in Scotland.
Research Interests
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.

50. Cystic Fibrosis
cystic fibrosis affects the lungs and makes it hard to breathe. Find out more in this article for kids.
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.

51. 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.
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

Human Brain Is Still Evolving

September 09, 2005
HHMI researchers who have analyzed sequence variations in two genes that regulate brain size in human populations have found evidence that the human brain is still evolving. More One Shot: Researchers Capture Pictures of Fusion Events That Enable Sperm to Penetrate Egg's Coating
September 05, 2005
Researchers have capitalized on the unique properties of a sperm cell to follow cell membrane fusion as it occurs during fertilization, tracking the full cascade of events for the first time. More Human Y Chromosome Preserves Itself Better Than the Chimp Y
September 01, 2005
By using human and chimpanzee Y chromosomes as a genetic fossil record to examine our past, scientists have seen a surprising difference in the way the male-making chromosomes from the two species cope with the inexorable pressures of evolution. More A New View of Human-Chimpanzee Genome Differences September 01, 2005

52. Cystic Fibrosis
cystic fibrosis (CF) is a genetic disorder that currently affects more than 30000 American children and young adults.

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.

53. Washington University Physicians Department Of Pediatrics
Information on this group of specialists for cystic fibrosis, NICU, growth disorders and other conditions.
HTTP/1.1 200 OK Server: Microsoft-IIS/5.0 Date: Fri, 09 Sep 2005 01:13:02 GMT Connection: close Content-Type: text/html
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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.
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
H. G. M. Heijerman

See editorial board for all editors information
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
Commenced publication 2002
Subscription for the year 2006, Volume 5, 4 issues

55. 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).

56. Cystic Fibrosis: What Is It?
Your Genes, Your Health, DNA Learning Center s multimedia guide to genetic, inherited disorders cystic fibrosis, autosomal recessive, mutation,

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.

57. 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.
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 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

58. 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)
Contact Us Sitemap document.write(navOptions[1]); for the treatment of hepatitis C, hepatitis B and certain cancers.
SciClone Reports Second Quarter 2005 Results

SciClone Presents Preclinical Data Demonstrating SCV-07's Activity in Human Papillomavirus and Lassa Fever Models
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

59. What Is Cystic Fibrosis? -
Article about diagnosis, symptoms, treatment and research on cystic fibrosis.
HOME VIDEOS RESOURCES NEWSLETTER ... SEARCH Search Site: Search Archives: HealingWell Conditions Cystic Fibrosis Library Article
What is Cystic Fibrosis
Every year, 1,000 children with cystic fibrosis (CF) are born in the United States. One in 3,000 Caucasian babies have the disorder, making CF one of the most common lethal genetic diseases in Caucasians. Overall, there are 30,000 Americans with CF, and an estimated 8 million people carry one copy of the defective gene that causes the disease. These carriers do not have symptoms of CF, because a person must inherit two defective gene copies-one from each parent-to develop the disease. However, each child of two CF carriers has a one in four chance of being born with CF. Genetic testing is now available to identify couples at risk for having children with CF.
Symptoms of Cystic Fibrosis
CF affects tissues that produce mucus secretions, such as the airway, the gastrointestinal tract, the ducts of the pancreas, the bile ducts of the liver and the male urogenital tract. Normal mucus forms a gel-like barrier that plays an important role in protecting the cells lining the inside surfaces of these tissues. In the lung, mucus also transports dust and other particles out of the airway and helps to prevent infection. CF alters the chemical properties of mucus; instead of protecting tissues from harm, the abnormal mucus obstructs the ducts and airways, causing tissue damage.

Develops antibacterial and antifungal drugs, including protegrins and related antimicrobial peptides, for application in cystic fibrosis. Includes pipeline, publications, and investor information from Palo Alto, California. (Nasdaq IBPI)

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