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Cystic Fibrosis - A Medical Dictionary, Bibliography, and Annotated Research Guide to Internet References
from: ICON Health Publications
: :In March 2001, the National Institutes of Health issued the following warning: 'The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading.' Furthermore, because of the rapid increase in Internet-based information, many hours can be wasted searching, selecting, and printing.This book was created for medical professionals, students, and members of the general public who want to conduct medical research using the most advanced tools available and spending the least amount of time doing so.
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Cystic Fibrosis and DNA Tests: Implications of Carrier Screening
from: Office of Technology Assessment
: :In March 2001, the National Institutes of Health issued the following warning: 'The number of Web sites offering health-related resources grows every day. Many sites provide valuable information, while others may have information that is unreliable or misleading.' Furthermore, because of the rapid increase in Internet-based information, many hours can be wasted searching, selecting, and printing.This book was created for medical professionals, students, and members of the general public who want to conduct medical research using the most advanced tools available and spending the least amount of time doing so.
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Cystic Fibrosis and Lung Transplantation: Ethical Concerns.(Statistical Data Included): An article from: Pediatric Nursing
: :This digital document is an article from Pediatric Nursing, published by Jannetti Publications, Inc. on January 1, 2001. The length of the article is 2698 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.Citation DetailsTitle: Cystic Fibrosis and Lung Transplantation: Ethical Concerns.(Statistical Data Included)Author: Diane Dickinson-HerbstPublication: Pediatric Nursing (Refereed)Date: January 1, 2001Publisher: Jannetti Publications, Inc.Volume: 27 Issue: 1 Page: 87Article ...
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Cystic Fibrosis And You
: :This digital document is an article from Pediatric Nursing, published by Jannetti Publications, Inc. on January 1, 2001. The length of the article is 2698 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.Citation DetailsTitle: Cystic Fibrosis and Lung Transplantation: Ethical Concerns.(Statistical Data Included)Author: Diane Dickinson-HerbstPublication: Pediatric Nursing (Refereed)Date: January 1, 2001Publisher: Jannetti Publications, Inc.Volume: 27 Issue: 1 Page: 87Article ...
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Cystic fibrosis can surface in adults.(late diagnosis consequences) : An article from: Internal Medicine News
: :This digital document is an article from Internal Medicine News, published by Thomson Gale on March 1, 2006. The length of the article is 885 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.Citation DetailsTitle: Cystic fibrosis can surface in adults.(late diagnosis consequences)Author: Timothy F. KirnPublication: Internal Medicine News (Magazine/Journal)Date: March 1, 2006Publisher: Thomson GaleVolume: 39 Issue: 5 Page: 1(2)Distributed ...
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Cystic fibrosis diagnosis after age 40 on the rise.(Pulmonary Medicine): An article from: Family Practice News
: :This digital document is an article from Family Practice News, published by Thomson Gale on February 15, 2006. The length of the article is 778 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.Citation DetailsTitle: Cystic fibrosis diagnosis after age 40 on the rise.(Pulmonary Medicine)Author: Timothy F. KirnPublication: Family Practice News (Magazine/Journal)Date: February 15, 2006Publisher: Thomson GaleVolume: 36 Issue: 4 ...
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CYSTIC FIBROSIS FOUNDATION AWARDS $21 MILLION TO VERTEX.: An article from: Biotech Financial Reports
from: Worldwide Videotex
: :This digital document is an article from Biotech Financial Reports, published by Worldwide Videotex on July 1, 2004. The length of the article is 839 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.Citation DetailsTitle: CYSTIC FIBROSIS FOUNDATION AWARDS $21 MILLION TO VERTEX.Publication: Biotech Financial Reports (Newsletter)Date: July 1, 2004Publisher: Worldwide VideotexVolume: 11 Issue: 7 Page: NADistributed by Thomson Gale
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Cystic Fibrosis in Adults
from: Lippincott Williams & Wilkins
: :Univ. of North Carolina, Chapel Hill. Comprehensive text for the diagnosis and care of adults with cystic fibrosis. Text is organized by the organ systems most affected by CF: molecular and cellular bases of disease pathogenesis, pulmonary disease, gastrointestinal system, and other organ systems. Extensively referenced. DNLM: Cystic Fibrosis--in adulthood.
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Cystic Fibrosis in the 20th Century: People, Events, and Progress
from: AM Publishing, Ltd.
: :More than just a history, this book provides a unique blend of science, clinical concerns, and warm personal accounts for the benefit of all who have been touched by Cystic Fibrosis. It tells the compelling story of the efforts of investigators, clinicians, and members of the CF community, documenting the rapid progress of research and treatment and dramatic improvement in survival rates since the first description of the disease in 1938. The editor has created a highly readable and well-organized tale in 32 stand-alone chapters, drawing on the heartfelt words ...
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Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution.: An article from: Human Biology
: :This digital document is an article from Human Biology, published by Wayne State University Press on August 1, 1997. The length of the article is 3741 words. The page length shown above is based on a typical 300-word page. The article is delivered in HTML format and is available in your Digital Locker immediately after purchase. You can view it with any web browser.From the author: KEY WORDS: CYSTIC FIBROSIS, RFLP, HAPLOTYPES, DF508, DNA, BRAZILCitation DetailsTitle: Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution.Author: Salmo ...
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