Sphingolipids as targets for inhalation treatment of cystic fibrosis-Reference-Cited by-同舟云学术

Sphingolipids as targets for inhalation treatment of cystic fibrosis

Published:2018-08 Issue: Volume:133 Page:66-75
ISSN:0169-409X
Container-title:Advanced Drug Delivery Reviews
language:en
Short-container-title:Advanced Drug Delivery Reviews

Author:

Becker Katrin Anne,Riethmüller Joachim,Seitz Aaron P.,Gardner Aaron,Boudreau Ryan,Kamler Markus,Kleuser Burkhard,Schuchman Edward,Caldwell Charles C.,Edwards Michael J.,Grassmé Heike,Brodlie Malcolm,Gulbins Erich

Funder

DFG

BMBF

NIH

Publisher

Elsevier BV

Subject

Pharmaceutical Science

Reference97 articles.

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2. Cystic fibrosis;Elborn;Lancet,2016

3. Gastro-intestinal manifestations in cystic fibrosis patients;Van Biervliet;Acta Gastroenterol. Belg.,2016

4. Rate of improvement of CF life expectancy exceeds that of general population-observational death registration study;Hurley;J. Cyst. Fibros.,2014

5. Patient Registry Annual Report;CF foundation,2010

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