NIH Consensus Development Conference on Genetic Testing for Cystic Fibrosis: April 14-16, 1997, Natcher Conference Center, National Institutes of Health, Bethesda, Md, Número 691National Institutes of Health, Continuing Medical Education, 1997 - 107 páginas |
Términos y frases comunes
airway alleles assay carrier population screening carrier status Caucasian CBAVD CF alleles CF carrier screening CF carrier testing CF mutations CF patients CF screening CF siblings CF testing CFTR gene child with CF chloride channel clinical cost couple screening cystic fibrosis carrier cystic fibrosis CF cystic fibrosis transmembrane decision Department of Pediatrics detection rate disorders dot blot education and testing effect epithelial Fanos fibrosis carrier screening Fibrosis Carrier Testing frequency genetic counseling genetic testing Genome Research Institute Grody WW haplotype Health Bethesda heterozygote Hispanic Holtzman Hum Genet Human Genome Research identified Institutes of Health large numbers lung disease Maryland MASDA molecular mutation detection National Human Genome negative neonatal screening newborn screening number of mutations oligonucleotide pancreatic partners Pediatrics Ph.D pregnancy pregnant women prenatal diagnosis prenatal screening probe Pueblo reported reproductive risk samples screening for CF screening for cystic sequencing sweat testing Tatsugawa test results therapy Zuni
Pasajes populares
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Página 27 - It will diminish the usual complaints of frequent, loose, foul movements, protuberant abdomen and excessive appetite, it will markedly reduce the incidence of rectal prolapse and possibly secondary fecal impaction which may result in intestinal obstruction."* "Schwachman, H.. Redmond. A. and Khaw. KT: "Studies in Cystic Fibrosis— Report of 130 Patients Diagnosed Under 3 Months of Age Over a 20-Year Period : Pediatrics.
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Página 9 - Program Analyst Office of Medical Applications of Research National Institutes of Health Bethesda, Maryland Suzanne W.
Página 9 - Branch National Institute of Diabetes and Digestive and Kidney Diseases National Institutes of Health Bethesda, Maryland KENNETH V.
Página 20 - A novel mutation in the cystic fibrosis gene in patients with pulmonary disease but normal sweat chloride concentrations. N Engl J Med 1994; 331:974-980.