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Cystectomies -- See Cystectomy


Used for excision of the urinary bladder 		  1
 

Cystectomy -- See Also Urinary Diversion


Temporary or permanent diversion of the flow of urine through the ureter away from the URINARY BLADDER in the presence of a bladder disease or after cystectomy. There is a variety of techniques: direct anastomosis of ureter and bowel, cutaneous ureterostomy, ileal, jejunal or colon conduit, ureterosigmoidostomy, etc. (From Campbell's Urology, 6th ed, p2654) 		  1
Cystectomy : Keys to successful orthotopic bladder substitution / Urs E. Studer, editor  2015 1
Cystectomy -- methods : Endourological management of urogenital carcinoma / S. Naito, Y. Hirao, T. Terachi (eds.)  2006 1
Cysteine Endopeptidases   7
Cysteine Proteases   2
Cysteine Proteases -- chemistry : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine Proteases -- immunology : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine Proteinase Inhibitors   3
 

Cysteine proteinases -- See Also the narrower term Calpain


  1
Cysteine proteinases.   7
 

Cysteine proteinases Inhibitors -- See Also the narrower term Cystatins


  1
Cysteine proteinases -- Inhibitors.   4
Cysteine proteinases -- Pathophysiology : Cysteine proteases of pathogenic organisms / edited by Mark W. Robinson, John P. Dalton  2011 1
Cysteine -- Therapeutic use : The therapeutic use of N-Acetylcysteine (NAC) in medicine / Richard Eugene Frye, Michael Berk, editors  2019 1
 

Cystic disease of the kidney -- See Kidney, Cystic


  1
 

Cystic Echinocccoses -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation 		  1
 

Cystic Echinocccosis -- See Echinococcosis


An infection caused by the infestation of the larval form of tapeworms of the genus Echinococcus. The liver, lungs, and kidney are the most common areas of infestation 		  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
Cystic fibrosis.   41
Cystic Fibrosis Association of Victoria. / http://id.loc.gov/authorities/names/n00138148 : Cystic fibrosis handbook / Teresa Bennington ... [and others]  1998 1
Cystic fibrosis -- Australia -- Victoria. : Cystic fibrosis care : quality of care guidelines / recommendations of the Victorian Clinical Standards Advisory Group on Cystic Fibrosis  1999 1
Cystic Fibrosis -- complications   2
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
Cystic Fibrosis -- diagnosis   3
Cystic fibrosis -- Diet therapy : Diet and exercise in cystic fibrosis / edited by Ronald Ross Watson  2015 1
Cystic fibrosis -- Diet therapy -- Recipes. : Target 100% plus : nutrition = energy + growth : cystic fibrosis / [written by Lynne Daniels ... and others]  1992? 1
Cystic fibrosis -- Exercise therapy : Diet and exercise in cystic fibrosis / edited by Ronald Ross Watson  2015 1
Cystic fibrosis -- Family relationships. : The family life of sick children : a study of families coping with chronic childhood disease / Lindy Burton  1975 1
Cystic fibrosis -- Genetic aspects.   3
Cystic Fibrosis -- genetics   2
Cystic fibrosis -- History : Dorothy Hansine Andersen : the life and times of the pioneering physician-scientist who identified cystic fibrosis / John Scott Baird  2022 1
Cystic fibrosis in children.   8
Cystic fibrosis in children-Diagnosis-France : The Birth of a Genetics Policy : Social Issues of Newborn Screening  2016 1
Cystic fibrosis in children -- Fiction : The NHS Experience : the 'Snakes and Ladders' guide for patients and professionals  2005 1
Cystic fibrosis in children -- Nutritional aspects. : Cystic fibrosis : nutritional and intestinal disorders / authors, Ross W. Shepherd and Geoffrey J. Cleghorn  1989 1
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
Cystic fibrosis in children -- Patients -- United States -- Biography. : Alex, the life of a child / Frank Deford  1983 1
Cystic fibrosis in children -- Popular works.   5
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
Cystic fibrosis in children -- Religious aspects. : The Family Life of Sick Children A Study of Families Coping with Chronic Childhood Disease  2022 1
Cystic fibrosis in children -- Research -- Case studies. : Questionnaires and Online Interviews : Exploring the Educational Experiences of Children With Cystic Fibrosis / Gathercole  2017 1
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
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
Cystic fibrosis -- Juvenile literature. : Cystic fibrosis / edited by Marcus A. Mall and J. Stuart Elborn  2014 1
Cystic fibrosis -- Laboratory manuals : Cystic fibrosis methods and protocols / edited by William R. Skach  2002 1
Cystic fibrosis -- Molecular aspects : Defects of secretion in cystic fibrosis / edited by Carsten Schultz  2005 1
Cystic fibrosis -- Molecular aspects -- Congresses : Defects of secretion in cystic fibrosis / edited by Carsten Schultz  2005 1
Cystic fibrosis -- Nutritional aspects : Nutrition in cystic fibrosis : a guide for Clinicians / Elizabeth H. Yen, Amanda Radmer Leonard, editors  2015 1
 

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
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