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Acta Medica Portuguesa|June 16, 2011
[The new face of Portuguese medicine: the generation of 1911 and the research school of Marck Athias]Isabel Maria AmaralDie Naturwissenschaften|November 22, 2007
Mechanical analysis of infant carrying in hominoidsLia Q AmaralPediatric Pulmonology|March 15, 2005
Processing of CFTR: traversing the cellular maze--how much CFTR needs to go through to avoid cystic fibrosis?Margarida D AmaralJournal of Inherited Metabolic Disease|June 10, 2006
Therapy through chaperones: sense or antisense? Cystic fibrosis as a model diseaseMargarida D AmaralJournal of Internal Medicine|October 1, 2014
Novel personalized therapies for cystic fibrosis: treating the basic defect in all patientsM D AmaralEuropean Journal of Medicinal Chemistry|November 16, 2020
How to determine the mechanism of action of CFTR modulator compounds: A gateway to theranosticsMargarida D AmaralPlastic and Reconstructive Surgery|April 30, 2019
Fat Grafting in Managing Craniofacial DeformitiesRafael Denadai, Cesar Augusto Raposo-Amaral, Cassio Eduardo Raposo-AmaralAdvances and Technical Standards in Neurosurgery|June 15, 2023
Apert Syndrome: Selection Rationale for Midface Advancement TechniqueCassio Eduardo Raposo-Amaral, Enrico Ghizoni, Cesar Augusto Raposo-AmaralBiological Psychiatry|January 22, 2002
The primate amygdala and the neurobiology of social behavior: implications for understanding social anxietyDavid G AmaralFoods (Basel, Switzerland)|January 20, 2021
Target and Non-Target Approaches for Food Authenticity and TraceabilityJoana S AmaralPageof 17,509