Pranke, Iwona M.

Correction of CFTR function in nasal epithelial cells from cystic fibrosis patients predicts improvement of respiratory function by CFTR modulators

Pranke, I. M., Hatton, A., Simonin, J., Jais, J. P., Le Pimpec-Barthes, F., Carsin, A., Bonnette, P., Fayon, M., Stremler-Le Bel, N., Grenet, D., et al. (2017) · Scientific Reports

Cystic Fibrosis Research AdvancesInhalation and Respiratory Drug Delivery

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Might Brushed Nasal Cells Be a Surrogate for CFTR Modulator Clinical Response?

Pranke, I., Hatton, A., Masson, A., Flament, T., Le Bourgeois, M., Chedevergne, F., Bailly, C., Urbach, V., Hinzpeter, A., Edelman, A., et al. (2019) · American Journal of Respiratory and Critical Care Medicine

Cystic Fibrosis Research AdvancesInhalation and Respiratory Drug Delivery

Cited by 50