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Angewandte Chemie (International Ed. in English)|May 12, 2020
Photocatalytic α-Tertiary Amine Synthesis via C-H Alkylation of Unmasked Primary AminesAlison S H Ryder, William B Cunningham, George Ballantyne, et al.
Wellcome Open Research|July 21, 2018
Can improved diagnostics reduce mortality from Tuberculous meningitis? Findings from a 6.5-year cohort in UgandaFiona V Cresswell, Ananta S Bangdiwala, Nathan C Bahr, et al.
Nature Communications|December 18, 2023
Recently activated CD4 T cells in tuberculosis express OX40 as a target for host-directed immunotherapyAbigail R Gress, Christine E Ronayne, Joshua M Thiede, et al.
Nature Genetics|September 4, 2020
Subclonal reconstruction of tumors by using machine learning and population geneticsGiulio Caravagna, Timon Heide, Marc J Williams, et al.
Prenatal Diagnosis|September 3, 2010
Barth syndrome: an X-linked cause of fetal cardiomyopathy and stillbirthC G Steward, R A Newbury-Ecob, R Hastings, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|May 25, 2023
The Pain in Dystonia Scale (PIDS)-Development and Validation in Cervical DystoniaVeronica Bruno, Beatrice Achen, Francesca Morgante, et al.
European Journal of Psychotraumatology|July 28, 2026
Understanding mental health needs in Ukraine: protocol for a longitudinal survey of mental health in children and caregivers during the war in UkraineRichard A Bryant, Iryna Shtefen, Oleh Romanchuk, et al.
International Journal of STD & AIDS|April 20, 2019
Cognitive function, depressive symptoms and syphilis in HIV-positive and HIV-negative individualsDavide De Francesco, Alan Winston, Jonathan Underwood, et al.
Health Expectations : an International Journal of Public Participation in Health Care and Health Policy|March 26, 2026
Getting It Out There: Reflections on the Process and Impact of Public Engagement Activities in a Study on End-of-Life Care Planning With People With Intellectual DisabilitiesAndrea Bruun, Amanda Cresswell, David Jeffrey, et al.
European Journal of Human Genetics : EJHG|October 18, 2007
8p23.1 duplication syndrome; a novel genomic condition with unexpected complexity revealed by array CGHJohn C K Barber, Viv K Maloney, Shuwen Huang, et al.
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