Researchers have developed a simple urine test to measure the severity of the serious disease cystic fibrosis and assess the effect of new treatments. Researchers have developed a simple urine test to ...
An easy-to-administer electrolyte test could offer new insight into response to treatment and disease progression for patients with cystic fibrosis. In a new study, researchers found that urine ...
Peak nasal inspiratory flow (PNIF) measurement was a feasible, noninvasive method for assessing nasal airflow obstruction in children with cystic fibrosis and correlated significantly with nasal ...
North Carolina has joined 46 states in adding Cystic Fibrosis testing for all newborns. Typically, the inherited, chronic disease isn't diagnosed until a child starts to show symptoms. However, with ...
Cystic fibrosis is missed more often in newborn screenings for non-white than white babies, creating higher risk for irreversible lung damage and other serious outcomes in Black, Hispanic, Asian, ...
The United States Cystic Fibrosis Foundation released the first guideline on newborn screening for cystic fibrosis (CF), in order to improve timely detection of CF in infants from all racial and ...
Owlstone Medical ("Owlstone"), the global leader in Breath Biopsy ® for applications in early disease detection and precision medicine, today announced that the Cystic Fibrosis Foundation has made an ...
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