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ΔF508
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11	[removed]Cystic Fibrosis MH.indd Add to Reading List Source URL: www.tcag.ca Language: English - Date: 2009-07-09 10:39:50 Medical genetics Pancreas disorders Pediatrics Cystic fibrosis ΔF508 Cystic Fibrosis Trust Gene therapy Heterozygote advantage Ivacaftor Biology Genetics Health
12	October — December 2009 Issue 46 INSIDE THIS ISSUE: H1n1 (Swine Flu) 2 Add to Reading List Source URL: www.cfedmonton.ca Language: English - Date: 2010-02-26 14:47:53 Channelopathy Cystic fibrosis Pediatrics Cystic Fibrosis Foundation Ivacaftor Denufosol ΔF508 Epithelial sodium channel Great Strides Biology Health Medicine
13	2012 Annual Report The Canadian Cystic Fibrosis Registry Add to Reading List Source URL: www.cysticfibrosis.ca Language: English - Date: 2014-03-05 17:33:39 Kin Canada Biology Cystic fibrosis ΔF508 Cystic Fibrosis Foundation Cystic Fibrosis Trust Health Medicine Cystic Fibrosis Canada
14	Traditional and Human Genome Variation Society (HGVS) Standard Nomenclature for Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Mutations and Variants Included on the Michigan Newbo Add to Reading List Source URL: www.michigan.gov Language: English - Date: 2013-01-08 07:53:12 Mutation Channelopathy Pediatrics ΔF508 Cystic fibrosis 1G Ivacaftor Biology Health Genetics
15	Cystic Fibrosis What is cystic fibrosis? Cystic fibrosis (CF) is a lifelong, hereditary disease that causes thick, sticky mucus to form in the lungs, pancreas and other organs. In the lungs, this mucus blocks the airway Add to Reading List Source URL: www.lung.org Language: English - Date: 2010-05-13 15:51:12 Channelopathy Cystic fibrosis Pediatrics Cystic Fibrosis Foundation ΔF508 Lung transplantation Sweat test Respiratory disease Cystic Fibrosis Trust Medicine Health Biology
16	Parent Fact Sheet Cystic Fibrosis (CF) (Sis-tick Fi-BRO-sis) What is CF? Cystic Fibrosis (CF) is a metabolic disorder. This means the body has a chemical imbalance. CF is a Add to Reading List Source URL: www.vdh.virginia.gov Language: English - Date: 2014-04-08 11:12:59 Channelopathy Cystic fibrosis Pediatrics Mucus Cystic Fibrosis Trust ΔF508 Health Anatomy Medicine
17	Reporting Reference Ranges for Cystic Fibrosis (CF) “<” “≤” “>” “≥” Add to Reading List Source URL: health.mo.gov Language: English - Date: 2012-12-13 12:12:15 Rare diseases Channelopathy Cystic fibrosis Pediatrics Mutation Point mutation ΔF508 Health Biology Genetics
18	PRIOR AUTHORIZATION POLICY Kalydeco® (ivacaftor tablets Vertex) To Initiate a Coverage Review, Call[removed] Add to Reading List Source URL: statehealthplan.state.nc.us Language: English - Date: 2014-04-24 08:24:08 Anilides Ivacaftor Phenols Quinolones Pancreas disorders Cystic fibrosis ΔF508 VX-809 Vertex Pharmaceuticals Biology Health Genetics
19	Missouri Department of Health and Senior Services P.O. Box 570, Jefferson City, MO[removed]Phone: [removed]FAX: [removed]RELAY MISSOURI for Hearing and Speech Impaired[removed]VOICE[removed]Gail Add to Reading List Source URL: health.mo.gov Language: English - Date: 2012-12-14 15:09:30 Mutation Channelopathy Pediatrics ΔF508 Cystic fibrosis transmembrane conductance regulator Cystic fibrosis 1G Health Genetics Biology
20	Cystic Fibrosis (CF) Cystic Fibrosis (CF) is a lifelong, hereditary disease that causes thick, sticky mucus to form in the lungs, pancreas, and other organs. In the lungs, this mucus blocks the airways, causing lung dama Add to Reading List Source URL: www.lung.org Language: English - Date: 2010-03-26 16:47:24 Rare diseases Biology Channelopathy Cystic fibrosis Cystic Fibrosis Foundation Sweat test Genetic disorder ΔF508 Public health genomics Health Medicine Pediatrics