Henry Levison

Cystic fibrosis patients bearing both the common missense mutation, Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus

Hamosh, Ada, King, Terri M., Rosenstein, Beryl J., Corey, Mary, Levison, Henry, Durie, Peter, ...

The glycine-to-aspartic acid missense mutation at codon 551 (G551D), which is within the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator (CFTR), is the third...

Cystic fibrosis patients bearing both the common missense mutation, Gly→Asp at codon 551 and the ΔF508 mutation are clinically indistinguishable from ΔF508 homozygotes, except for decreased risk of meconium ileus

Hamosh, Ada, King, Terri M., Rosenstein, Beryl J., Corey, Mary, Levison, Henry, Durie, Peter, ...

The glycine-to-aspartic acid missense mutation at codon 551 (G551D), which is within the first nucleotide-binding fold of the cystic fibrosis transmembrane conductance regulator (CFTR), is the third...

The Effect of Isoproterenol on Airway Obstruction in Cystic Fibrosis

Featherby, Elizabeth A., Weng, Tzong-Ruey, Levison, Henry

The effect of isoproterenol inhalations was studied on 95 occasions in 47 patients with cystic fibrosis.