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Parasites & Vectors|December 12, 2022
Drugs for neglected tropical diseases: availability of age-appropriate oral formulations for young childrenIssraa Al-Obaidi, Anna K Krome, Karl G Wagner, et al.
European Journal of Human Genetics : EJHG|October 18, 2012
CLCA4 variants determine the manifestation of the cystic fibrosis basic defect in the intestineErnst-Wolfgang Kolbe, Stephanie Tamm, Silke Hedtfeld, et al.
European Journal of Human Genetics : EJHG|April 5, 2007
Transmission ratio distortion and maternal effects confound the analysis of modulators of cystic fibrosis disease severity on 19q13Tim Becker, Silke Jansen, Stephanie Tamm, et al.
Surgery in Practice and Science|January 23, 2025
A comparison of open or laparoscopic colectomy outcomes for the management of ischemic colitis using the ACS-NSQIP databaseBen S Duggan, Tim Becker, Genaro A DeLeon, et al.
European Journal of Dental Education : Official Journal of the Association for Dental Education in Europe|November 28, 2025
Choosing Wisely: Key Feature Examinations as a Powerful Approach to Foster Clinical Reasoning in Dental EducationMarc André Ackermann, Tim Becker, Nima Gholamzadeh Biji, et al.
European Journal of Human Genetics : EJHG|October 10, 2013
The CF-modifying gene EHF promotes p.Phe508del-CFTR residual function by altering protein glycosylation and trafficking in epithelial cellsFrauke Stanke, Andrea van Barneveld, Silke Hedtfeld, et al.
International Journal of Pharmaceutics: X|April 14, 2021
In vitro and in vivo assessment of hydroxypropyl cellulose as functional additive for enabling formulations containing itraconazoleRafael D Bachmaier, Marius Monschke, Thilo Faber, et al.
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