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1  

Cystic Fibrosis -- See Also Cystic Fibrosis Transmembrane Conductance Regulator


A chloride channel that regulates secretion in many exocrine tissues. Abnormalities in the CFTR gene have been shown to cause cystic fibrosis. (Hum Genet 1994;93(4):364-8)
  1
2 Cystic fibrosis.   37
3 Cystic Fibrosis Association of Victoria. / http://id.loc.gov/authorities/names/n00138148 : Cystic fibrosis handbook / Teresa Bennington ... [and others]  1998 1
4 Cystic fibrosis -- Australia -- Victoria. : Cystic fibrosis care : quality of care guidelines / recommendations of the Victorian Clinical Standards Advisory Group on Cystic Fibrosis  1999 1
5 Cystic Fibrosis -- complications.   3
6 Cystic fibrosis -- Congresses. : Current problems and new trends in cystic fibrosis : 10th meeting of the European Working Group for Cystic Fibrosis, Bern, September 22-23, 1981 / volume editors: M. Schoni and R. Kraemer  1981 1
7 Cystic fibrosis -- Diet therapy -- Recipes. : Target 100% plus : nutrition = energy + growth : cystic fibrosis / [written by Lynne Daniels ... and others]  1992? 1
8 Cystic Fibrosis -- drug therapy. : Infection in the cystic fibrosis lung / J. Stuart Elborn  2014 1
9 Cystic fibrosis -- Family relationships. : The family life of sick children : a study of families coping with chronic childhood disease / Lindy Burton  1975 1
10 Cystic fibrosis gene : Genetic Diseases or Conditions : Cystic Fibrosis, The Salty Kiss  2016 1
11 Cystic fibrosis -- Genetic aspects.   4
12 Cystic Fibrosis -- genetics. : Cystic fibrosis in the 21st century / volume editors, Andrew Bush [and others]  2006 1
13 Cystic fibrosis in children.   8
14 Cystic fibrosis in children-Diagnosis-France : The Birth of a Genetics Policy : Social Issues of Newborn Screening  2016 1
15 Cystic fibrosis in children -- Fiction : The NHS experience : the "snakes and ladders" guide for patients and professionals / Hilary Cass  2006 1
16 Cystic fibrosis in children -- Nutritional aspects. : Cystic fibrosis : nutritional and intestinal disorders / authors, Ross W. Shepherd and Geoffrey J. Cleghorn  1989 1
17 Cystic fibrosis in children -- Oman. : Cystic fibrosis in children of the eastern Arabian peninsula : a clinical, spatial and genetic study / by Kenneth P. Dawson  2003 1
18 Cystic fibrosis in children -- Patients -- United States -- Biography. : Alex, the life of a child / Frank Deford  1983 1
19 Cystic fibrosis in children -- Popular works.   4
20 Cystic fibrosis in children -- Psychological aspects. : The family life of sick children : a study of families coping with chronic childhood disease / Lindy Burton  1975 1
21 Cystic fibrosis in children -- Research -- Case studies. : Questionnaires and Online Interviews : Exploring the Educational Experiences of Children With Cystic Fibrosis / Gathercole  2017 1
22 Cystic fibrosis in children -- Social aspects. : The family life of sick children : a study of families coping with chronic childhood disease / Lindy Burton  1975 1
23 Cystic fibrosis in children -- United Arab Emirates. : Cystic fibrosis in children of the eastern Arabian peninsula : a clinical, spatial and genetic study / by Kenneth P. Dawson  2003 1
24 Cystic fibrosis -- Juvenile literature. : Cystic fibrosis / edited by Marcus A. Mall and J. Stuart Elborn  2014 1
25 Cystic Fibrosis -- metabolism. : Role of ER stress in cystic fibrosis airway inflammation / Carla M. P. Ribeiro  2012 1
26 Cystic Fibrosis -- microbiology. : Infection in the cystic fibrosis lung / J. Stuart Elborn  2014 1
27 Cystic fibrosis -- Molecular aspects. : Defects of secretion in cystic fibrosis / edited by Carsten Schultz  2005 1
28 Cystic fibrosis -- Nutritional aspects.   2
29  

Cystic Fibrosis of Pancreas -- See Cystic Fibrosis


An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION
  1
30  

Cystic Fibrosis, Pancreatic -- See Cystic Fibrosis


An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION
  1
31 Cystic fibrosis -- Pathophysiology. : Defects of secretion in cystic fibrosis / edited by Carsten Schultz  2005 1
32 Cystic fibrosis -- Patient : Cystic fibrosis : adolescence : speaking from experience    1
33 Cystic fibrosis -- Patients.   9
34 Cystic fibrosis -- Patients -- Biography.   2
35 Cystic fibrosis -- Patients -- Family relationships. : The family life of sick children : a study of families coping with chronic childhood disease / Lindy Burton  1975 1
36 Cystic fibrosis -- Patients -- Family relationships -- United States. : The power of two : a twin triumph over cystic fibrosis / Isabel Stenzel Byrnes & Anabel Stenzel  2014 1
37 Cystic fibrosis -- Patients -- Fiction : The NHS experience : the "snakes and ladders" guide for patients and professionals / Hilary Cass  2006 1
38 Cystic fibrosis -- Patients -- New Zealand -- Biography. : Silent fighters : cystic fibrosis in New Zealand / photography by Myra Hauschild  1996 1
39 Cystic fibrosis -- Patients -- United States -- Biography. : The power of two : a twin triumph over cystic fibrosis / Isabel Stenzel Byrnes & Anabel Stenzel  2014 1
40 Cystic fibrosis -- Periodicals   2
41 Cystic Fibrosis -- physiopathology.   3
42 Cystic fibrosis -- Popular works.   3
43 Cystic fibrosis -- Psychological aspects.   5
44 Cystic Fibrosis -- psychology. : Psychosocial aspects of cystic fibrosis / edited by Myra Bluebond-Langner, Bryn Lask, Denise B. Angst  2001 1
45 Cystic fibrosis -- Public opinion -- Research -- Case studies. : User-driven data capture : locating and analysing Twitter conversation about cystic fibrosis without keywords / Phillip Brooker & Julie Barnett & Timothy Cribbin & Alexandra R. Lang & Jennifer Martin  2014 1
46  

Cystic Fibrosis, Pulmonary -- See Cystic Fibrosis


An autosomal recessive genetic disease of the EXOCRINE GLANDS. It is caused by mutations in the gene encoding the CYSTIC FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR expressed in several organs including the LUNG, the PANCREAS, the BILIARY SYSTEM, and the SWEAT GLANDS. Cystic fibrosis is characterized by epithelial secretory dysfunction associated with ductal obstruction resulting in AIRWAY OBSTRUCTION; chronic RESPIRATORY INFECTIONS; PANCREATIC INSUFFICIENCY; maldigestion; salt depletion; and HEAT PROSTRATION
  1
47 Cystic fibrosis -- Research -- Case studies. : Questionnaires and Online Interviews : Exploring the Educational Experiences of Children With Cystic Fibrosis / Gathercole  2017 1
48 Cystic fibrosis -- Social aspects.   2
49 Cystic Fibrosis -- therapy.   2
50 Cystic Fibrosis Transmembrane Conductance Regulator.   2
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