Showing results (1671-1680 of 1,718) with videos related to

Sort By:
Pageof 172
Journal of Clinical Apheresis|March 27, 2025
A Descriptive 5-Year Analysis of the Demographics and Therapies for Patients With Immune Thrombotic Thrombocytopenic Purpura in the USA: A Multicenter Study of 390 Disease Episodes From 2017 to 2021Jeremy W Jacobs, Brian D Adkins, Garrett S Booth, et al.
Journal of the American Academy of Dermatology|April 29, 2022
Cross-sectional characteristics of pediatric-onset discoid lupus erythematosus: Results of a multicenter, retrospective cohort studyN Ezeh, K Ardalan, K A Buhr, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|July 19, 2021
International Consensus for the Dosing of Corticosteroids in Childhood-Onset Systemic Lupus Erythematosus With Proliferative Lupus NephritisNathalie E Chalhoub, Scott E Wenderfer, Deborah M Levy, et al.
Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences|August 15, 2018
The repeatability of cognitive performance: a meta-analysisM Cauchoix, P K Y Chow, J O van Horik, et al.
American Journal of Human Genetics|March 5, 2016
Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum DisordersHolly A F Stessman, Marjolein H Willemsen, Michaela Fenckova, et al.
American Journal of Human Genetics|July 27, 2021
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in DrosophilaLindsey D Goodman, Heidi Cope, Zelha Nil, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 19, 2017
Insights into the red algae and eukaryotic evolution from the genome of Porphyra umbilicalis (Bangiophyceae, Rhodophyta)Susan H Brawley, Nicolas A Blouin, Elizabeth Ficko-Blean, et al.
Advances in Experimental Medicine and Biology|September 16, 2024
Global Challenges After a Global Challenge: Lessons Learned from the COVID-19 PandemicNiloufar Yazdanpanah, Constantine Sedikides, Hans D Ochs, et al.
European Journal of Human Genetics : EJHG|January 26, 2019
De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphismsSandra Jansen, Ilse M van der Werf, A Micheil Innes, et al.
American Journal of Human Genetics|April 30, 2019
Mutations in ACTL6B Cause Neurodevelopmental Deficits and Epilepsy and Lead to Loss of Dendrites in Human NeuronsScott Bell, Justine Rousseau, Huashan Peng, et al.
Pageof 172