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PED5 Edema, hypoproteinemia, and acrodermatitis enteropathica: An uncommon initial presentation of cystic fibrosis. (Pediatrics and Adolescent Medicine).(Brief ... An article from: Southern Medical Journal
from: Southern Medical Association
: :This digital document is an article from Southern Medical Journal, published by Southern Medical Association on December 1, 2001. The length of the article is 799 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: PED5 Edema, hypoproteinemia, and acrodermatitis enteropathica: An uncommon initial presentation of cystic fibrosis. (Pediatrics and Adolescent Medicine).(Brief Article)Publication: Southern Medical Journal (Refereed)Date: December 1, ...
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Pediatric cystic fibrosis pain is understudied, undertreated.: An article from: Family Practice News
: :This digital document is an article from Family Practice News, published by Thomson Gale on November 1, 2006. The length of the article is 448 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: Pediatric cystic fibrosis pain is understudied, undertreated.Author: Betsy BatesPublication: Family Practice News (Magazine/Journal)Date: November 1, 2006Publisher: Thomson GaleVolume: 36 Issue: 21 Page: 52(1)Distributed by Thomson ...
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Preconception and Prenatal Carrier Screening for Cystic Fibrosis: Clinical and Laboratory Guidelines
from: Amer College of Obstetricians &
: :Addresses questions such as: Who are candidates for cystic fibrosis carrier screening? And what are the screening strategies and process?
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Prenatal screening halves cystic fibrosis births: carrier rate of 1 in 28.(Women's Health): An article from: Family Practice News
: :This digital document is an article from Family Practice News, published by International Medical News Group on January 1, 2004. The length of the article is 954 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: Prenatal screening halves cystic fibrosis births: carrier rate of 1 in 28.(Women's Health)Author: Betsy BatesPublication: Family Practice News (Magazine/Journal)Date: January 1, 2004Publisher: International ...
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Progress In Cystic Fibrosis Research
from: Nova Biomedical Books
: :Cystic fibrosis (CF), also known as munoviscidosis, is a chronic genetic disease involving the dysfunction of the exocrine glands. This dysfunction is manifested as a deficiency in pancreatic enzymes, accumulation of mucous in airways, and excess salt in sweat. Cystic fibrosis was previously restricted to infancy and childhood but developments in medical treatment and therapy have extended survival considerably. This book includes within its scope research aimed at understanding the genetic linkage in cystic fibrosis, as well as improving the diagnosis and treatment of this disease in both children and ...
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Psychosocial Aspects of Cystic Fibrosis; A Model for Chronic Lung Disease.
: :Cystic fibrosis (CF), also known as munoviscidosis, is a chronic genetic disease involving the dysfunction of the exocrine glands. This dysfunction is manifested as a deficiency in pancreatic enzymes, accumulation of mucous in airways, and excess salt in sweat. Cystic fibrosis was previously restricted to infancy and childhood but developments in medical treatment and therapy have extended survival considerably. This book includes within its scope research aimed at understanding the genetic linkage in cystic fibrosis, as well as improving the diagnosis and treatment of this disease in both children and ...
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Recent Advances in Cystic Fibrosis Research (Monographs in Paediatrics)
from: S Karger AG
: :Cystic fibrosis (CF), also known as munoviscidosis, is a chronic genetic disease involving the dysfunction of the exocrine glands. This dysfunction is manifested as a deficiency in pancreatic enzymes, accumulation of mucous in airways, and excess salt in sweat. Cystic fibrosis was previously restricted to infancy and childhood but developments in medical treatment and therapy have extended survival considerably. This book includes within its scope research aimed at understanding the genetic linkage in cystic fibrosis, as well as improving the diagnosis and treatment of this disease in both children and ...
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Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study.: An article from: Human Biology
: :This digital document is an article from Human Biology, published by Wayne State University Press on February 1, 1997. The length of the article is 5784 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, DNA, BRAZILCitation DetailsTitle: Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study.Author: Salmo RaskinPublication: Human ...
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Research on Pathogenesis of Cystic Fibrosis of the Pancreas (Mucoviscidosis)
: :This digital document is an article from Human Biology, published by Wayne State University Press on February 1, 1997. The length of the article is 5784 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, DNA, BRAZILCitation DetailsTitle: Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study.Author: Salmo RaskinPublication: Human ...
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Saline inhalation eases cystic fibrosis symptoms: the rehydration appears to produce a sustained acceleration of mucus clearance in the airways.(Pulmonary ... : 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 1008 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: Saline inhalation eases cystic fibrosis symptoms: the rehydration appears to produce a sustained acceleration of mucus clearance in the airways.(Pulmonary Medicine)Author: Mary Ann MoonPublication: Internal ...
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