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Environmental Health Perspectives|March 1, 2018
Maternal Plasma per- and Polyfluoroalkyl Substance Concentrations in Early Pregnancy and Maternal and Neonatal Thyroid Function in a Prospective Birth Cohort: Project Viva (USA)Emma V Preston, Thomas F Webster, Emily Oken, et al.Medical Hypotheses|November 17, 2009
Do dopaminergic gene polymorphisms affect mesolimbic reward activation of music listening response? Therapeutic impact on Reward Deficiency Syndrome (RDS)Kenneth Blum, Thomas J H Chen, Amanda L H Chen, et al.Journal of Neurosurgery. Spine|November 9, 2019
Nerve transfer for restoration of lower motor neuron-lesioned bladder and urethra function: establishment of a canine model and interim pilot study resultsEkta Tiwari, Danielle M Salvadeo, Alan S Braverman, et al.The EMBO Journal|January 4, 2024
Disease-associated polyalanine expansion mutations impair UBA6-dependent ubiquitinationFatima Amer-Sarsour, Daniel Falik, Yevgeny Berdichevsky, et al.Journal of the American Heart Association|February 26, 2026
Sex-Related Differences in Clinical Profile, Management, and Outcomes of Patients With Type A and B Acute Aortic Dissection: Observations From IRADElizabeth Jackson, Andreina Carbone, Sherene Shalhub, et al.American Journal of Medical Genetics. Part A|April 29, 2006
Familial thoracic aortic aneurysms and dissections: three families with early-onset ascending and descending aortic dissections in womenVan Tran-Fadulu, Julia H Chen, Danielle Lemuth, et al.Postgraduate Medicine|November 27, 2009
Neurogenetics of dopaminergic receptor supersensitivity in activation of brain reward circuitry and relapse: proposing "deprivation-amplification relapse therapy" (DART)Kenneth Blum, Thomas J H Chen, B William Downs, et al.Journal of Behavioral Addictions|July 14, 2015
Hypothesizing repetitive paraphilia behavior of a medication refractive Tourette's syndrome patient having rapid clinical attenuation with KB220Z-nutrigenomic amino-acid therapy (NAAT)Thomas Mclaughlin, Marlene Oscar-Berman, Thomas Simpatico, et al.Journal of Inherited Metabolic Disease|January 8, 2009
A PEX10 defect in a patient with no detectable defect in peroxisome assembly or metabolism in cultured fibroblastsS J Steinberg, A Snowden, N E Braverman, et al.Leukemia Research|August 5, 2022
Patient experience before and after treatment with idecabtagene vicleucel (ide-cel, bb2121): qualitative analysis of patient interviews in the KarMMa trialNina Shah, Michel Delforge, Jesus San-Miguel, et al.Pageof 166