Results 231 to 240 of about 69,585 (295)

NO pathway in CF and non‐CF children

Pediatric Pulmonology, 2004
AbstractControversy exists concerning abnormalities of the nitric oxide (NO) pathway in cystic fibrosis (CF) lung disease. Although some studies suggested that NO activity is impaired in CF, changes in NO production in young children have not been studied.
Jamie L, Wooldridge   +8 more
openaire   +2 more sources

ChemInform Abstract: Tetrafluoroferrole, (CO)3Fe‐cyclic(Fe‐CF=CF‐CF=CF)(CO)3.

ChemInform, 1988
AbstractThe title compound (IV) is obtained as a by‐product in the synthesis of the triiron complex (III) from pentacarbonyliron (I) and tribromofluoromethane (II).
D. LENTZ, H. MICHAEL
openaire   +1 more source

Atypical CF and CF related diseases

Paediatric Respiratory Reviews, 2006
The clinical characteristics of atypical CF are: symptoms that may start in infancy but the disease become clinically significant only after 10 years of age, survival into adulthood, chronic sinopulmonary disease, pancreatic sufficiency, and sweat chloride
openaire   +2 more sources

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