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European Journal of Pain (London, England)|December 2, 2021
Exploring patient preference heterogeneity for pharmacological treatments for chronic pain: A latent class analysisDavid A Walsh, Marco Boeri, Lucy Abraham, et al.
American Journal of Medical Genetics. Part A|August 5, 2015
A novel 2q37 microdeletion containing human neural progenitors genes including STK25 results in severe developmental delay, epilepsy, and microcephalyJaime Imitola, Divya S Khurana, Nadiya M Teplyuk, et al.
Journal of Immunology (Baltimore, Md. : 1950)|July 14, 2009
Atypical memory B cells are greatly expanded in individuals living in a malaria-endemic areaGreta E Weiss, Peter D Crompton, Shanping Li, et al.
Medicine|November 1, 1991
Comparison of patients with idiopathic calcium phosphate and calcium oxalate stonesM H Gault, L L Chafe, J M Morgan, et al.
Obesity (Silver Spring, Md.)|November 14, 2018
Intensive Behavioral Therapy for Obesity Combined with Liraglutide 3.0 mg: A Randomized Controlled TrialThomas A Wadden, Olivia A Walsh, Robert I Berkowitz, et al.
Research Square|February 24, 2023
Comorbidity burden and health-related quality of life in men with advanced prostate cancerRoberto Benzo, Patricia I Moreno, Rina S Fox, et al.
Clinical Genetics|April 2, 2023
A recurrent de novo variant in NUSAP1 escapes nonsense-mediated decay and leads to microcephaly, epilepsy, and developmental delayAlisa Mo, Emuna Paz-Ebstein, Shira Yanovsky-Dagan, et al.
Biorxiv : the Preprint Server for Biology|October 17, 2024
Perinatal Reduction of Genetically Aberrant Neurons from Human Cerebral CortexDiane D Shao, Yifan Zhao, Urmi Ghosh, et al.
Nature Biotechnology|January 8, 2020
Accurate detection of mosaic variants in sequencing data without matched controlsYanmei Dou, Minseok Kwon, Rachel E Rodin, et al.
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