Research in Cystic Fibrosis
- 9 September 1976
- journal article
- review article
- Published by Massachusetts Medical Society in New England Journal of Medicine
- Vol. 295 (11) , 597-602
- https://doi.org/10.1056/nejm197609092951105
Abstract
(Third of Three Parts)Autonomic Nervous SystemMost of the clinical features of cystic fibrosis are due to malfunction of exocrine glands, which are intimately associated with autonomic nerve fibers. Therefore, dysfunction of this system has always been an attractive explanation for this generalized exocrinopathy. However, the studies performed in the past have resulted in either negative or controversial findings.1 More recently, in 1973, a careful ultrastructure and histochemical study of autonomic nerve fibers in labial salivary glands from patients with cystic fibrosis failed to identify any differences from normal.143 Conversely, experimental studies using animal models have been more fruitful. . . .Keywords
This publication has 37 references indexed in Scilit:
- Serum -Fetoprotein in Cystic FibrosisBMJ, 1975
- Endocrine function of the pancreas in cystic fibrosis: Evidence for an impaired glucagon and insulin response following arginine infusionThe Journal of Pediatrics, 1974
- Studies on ciliary dyskinesia factor in cystic fibrosis. IV. Its possible identification as anaphylatoxin (C3a)-IgG complexLife Sciences, 1974
- Tear sodium, potassium, chloride, and calcium at various flow rates: Children with cystic fibrosis and unaffected siblings with and without corneal stainingThe Journal of Pediatrics, 1973
- Flow rate and inorganic components of submandibular saliva in cystic fibrosisArchives of Disease in Childhood, 1973
- Deficiency of Kallikrein Activity in Plasma of Patients with Cystic FibrosisScience, 1972
- Deficiency of trypsin-like activity in saliva of patients with cystic fibrosisThe Journal of Pediatrics, 1972
- Complications of iodide therapy in patients with cystic fibrosisThe Journal of Pediatrics, 1971
- Sodium concentration in unstimulated parotid saliva and on oral mucosa in normal subjects and in patients with cystic fibrosisThe Journal of Pediatrics, 1970
- Immunological studies of submaxillary saliva from patients with cystic fibrosis and from normal childrenThe Journal of Pediatrics, 1968