Showing results (491-500 of 509) with videos related to

Sort By:
Pageof 51
Endocrine Connections|June 20, 2013
Glucocorticoid sensitivity in Behçet's diseaseR A M Quax, J A M van Laar, R van Heerebeek, et al.
Frontiers in Allergy|May 30, 2024
Pre-asthma: a useful concept? A EUFOREA paper. Part 2-late onset eosinophilic asthmaG K Scadding, C Gray, D M Conti, et al.
Frontiers in Allergy|February 14, 2024
Pre-asthma: a useful concept for prevention and disease-modification? A EUFOREA paper. Part 1-allergic asthmaG K Scadding, M McDonald, V Backer, et al.
Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology|May 3, 2012
A common variant in ERBB4 regulates GABA concentrations in human cerebrospinal fluidJurjen J Luykx, Christiaan H Vinkers, Steven C Bakker, et al.
BMJ Paediatrics Open|February 24, 2026
Enhancing implementation and compliance of the Screening Instrument for Child Abuse and Neglect (SCAN) in emergency departments in the NetherlandsEline A L van den Heuvel, Erica de Vries, Brita M de Jong-van Kempen, et al.
Frontiers in Immunology|June 30, 2020
Behçet's Disease Under Microbiotic Surveillance? A Combined Analysis of Two Cohorts of Behçet's Disease PatientsTim B van der Houwen, Jan A M van Laar, Jasper H Kappen, et al.
Nature Communications|September 28, 2024
Tomography of entangling two-qubit logic operations in exchange-coupled donor electron spin qubitsHolly G Stemp, Serwan Asaad, Mark R van Blankenstein, et al.
Acta Neuropathologica|February 8, 2020
Niacin-mediated rejuvenation of macrophage/microglia enhances remyelination of the aging central nervous systemKhalil S Rawji, Adam M H Young, Tanay Ghosh, et al.
Acta Neuropathologica|March 27, 2020
Correction to: Niacin-mediated rejuvenation of macrophage/microglia enhances remyelination of the aging central nervous systemKhalil S Rawji, Adam M H Young, Tanay Ghosh, et al.
European Journal of Human Genetics : EJHG|August 18, 2016
Compound heterozygous NEK1 variants in two siblings with oral-facial-digital syndrome type II (Mohr syndrome)Glen R Monroe, Isabelle Fpm Kappen, Marijn F Stokman, et al.
Pageof 51