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Year | Number of Results |
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2004 | 1 |
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Page 1
New insights into the pathogenesis of cystic fibrosis: pivotal role of glutathione system dysfunction and implications for therapy.
Treat Respir Med. 2004;3(6):353-63. doi: 10.2165/00151829-200403060-00003.
Treat Respir Med. 2004.
PMID: 15658882
Review.
Oral reduced L-glutathione improves growth in pediatric cystic fibrosis patients.
Visca A, Bishop CT, Hilton S, Hudson VM.
Visca A, et al. Among authors: hudson vm.
J Pediatr Gastroenterol Nutr. 2015 Jun;60(6):802-10. doi: 10.1097/MPG.0000000000000738.
J Pediatr Gastroenterol Nutr. 2015.
PMID: 25633497
Clinical Trial.
Item in Clipboard
A pilot study of the effect of inhaled buffered reduced glutathione on the clinical status of patients with cystic fibrosis.
Bishop C, Hudson VM, Hilton SC, Wilde C.
Bishop C, et al. Among authors: hudson vm.
Chest. 2005 Jan;127(1):308-17. doi: 10.1378/chest.127.1.308.
Chest. 2005.
PMID: 15653998
Clinical Trial.
Item in Clipboard
Improvement in clinical markers in CF patients using a reduced glutathione regimen: an uncontrolled, observational study.
Visca A, Bishop CT, Hilton SC, Hudson VM.
Visca A, et al. Among authors: hudson vm.
J Cyst Fibros. 2008 Sep;7(5):433-6. doi: 10.1016/j.jcf.2008.03.006. Epub 2008 May 21.
J Cyst Fibros. 2008.
PMID: 18499536
Free article.
Item in Clipboard
Differing compartments of intracellular glutathione have differing levels of glutathione in cystic fibrosis.
Hudson VM.
Hudson VM.
Med Hypotheses. 2007;68(4):919-20. doi: 10.1016/j.mehy.2006.09.033. Epub 2006 Nov 13.
Med Hypotheses. 2007.
PMID: 17097824
No abstract available.
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