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Journal of Neurology, Neurosurgery, and Psychiatry|November 8, 2013
Novel C12orf65 mutations in patients with axonal neuropathy and optic atrophyArianna Tucci, Yo-Tsen Liu, Elisabeth Preza, et al.JMIR Research Protocols|September 25, 2024
Integrating Social Determinants of Health in Machine Learning-Driven Decision Support for Diabetes Case Management: Protocol for a Sequential Mixed Methods StudySeung-Yup Lee, Leslie W Hayes, Bunyamin Ozaydin, et al.The Journal of Infectious Diseases|March 24, 2009
A common CD4 gene variant is associated with an increased risk of HIV-1 infection in Kenyan female commercial sex workersJulius O Oyugi, Françoise C M Vouriot, Judie Alimonti, et al.Journal of Bacteriology|May 19, 2006
The genome of the obligately intracellular bacterium Ehrlichia canis reveals themes of complex membrane structure and immune evasion strategiesK Mavromatis, C Kuyler Doyle, A Lykidis, et al.Plos One|August 23, 2011
Uncovering genomic causes of co-morbidity in epilepsy: gene-driven phenotypic characterization of rare microdeletionsDalia Kasperavičiūtė, Claudia B Catarino, Krishna Chinthapalli, et al.Acta Psychiatrica Scandinavica|June 26, 2014
Staging systems in bipolar disorder: an International Society for Bipolar Disorders Task Force ReportF Kapczinski, P V S Magalhães, V Balanzá-Martinez, et al.Nature|February 8, 2013
APOBEC3B is an enzymatic source of mutation in breast cancerMichael B Burns, Lela Lackey, Michael A Carpenter, et al.Science (New York, N.Y.)|July 7, 2001
Human chromosome 19 and related regions in mouse: conservative and lineage-specific evolutionP Dehal, P Predki, A S Olsen, et al.Acta Psychiatrica Scandinavica|June 27, 2015
Obesity, but not metabolic syndrome, negatively affects outcome in bipolar disorderS L McElroy, D E Kemp, E S Friedman, et al.Orphanet Journal of Rare Diseases|July 9, 2013
SURF1 deficiency: a multi-centre natural history studyYehani Wedatilake, Ruth M Brown, Robert McFarland, et al.Pageof 42