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Unfortunately, around 30% of patients do not respond to the current available pharmacological treatments
Stored correctly, it remains stable until the manufacturers printed expiry date
Decreased GSH content in the apical fluid in cystic fibrosis could be the result of abnormal GSH transport associated with a defective cystic fibrosis transmembrane conductance regulator as mentioned previously (126)
What happens when treatment stops
Several lung disorders are believed to be characterized by an increase in alveolar oxidant burden, potentially depleting alveolar and lung GSH
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