Results 161 to 170 of about 50,093 (313)
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective Variants in SLC6A1, encoding the GABA transporter 1 (GAT‐1), cause epilepsy, autism spectrum disorder, and developmental delay via loss of GABA uptake, impaired trafficking, and ER retention. We previously found that 4‐Phenylbutyrate (PBA), an FDA‐approved drug, restores GABA uptake and reduces seizures in SLC6A1‐related disorders ...
Melissa B. DeLeeuw +5 more
wiley +1 more source
, 2019 Essay from book "Ukraine in Histories and Stories: Essays by Ukrainian intellectuals"
Yermolenko, Volodymyr
core
, 2020 You know how research takes a lo-ong time, and publication processes too? Let me tell you a story about it, and one that ends well at that. A decade ago, when the projet "Berlin intellectuals 1800-1830" started, there were three main focus points ...
Anne Baillot
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Adolescent sports participation and social-class health inequalities: evidence from CHNS. [PDF]
Front Public HealthYu J, Lu Y, Zhao L.
europepmc +1 more source
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Objective To clarify the clinical relevance of dopamine transporter single‐photon emission computed tomography (DAT‐SPECT) abnormalities in amyotrophic lateral sclerosis (ALS), with a prespecified focus on sex‐stratified associations with disease progression and short‐term prognosis.
Tomoya Kawazoe +7 more
wiley +1 more source
CfP INTELLECTUALS AND PUBLIC SPHERES
, 2010 Title: Call for Papers - International worskhop 'Intellectuals and public spheres', 24- 25 March 2011, Antwerp. Description: Please find below the call for papers for the upcoming international workshop on intellectuals and public spheres that UCSIA ...
Rogério Santos
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Cyber anti-intellectualism and science communication during the COVID-19 pandemic: a cross-sectional study. [PDF]
Front Public HealthKuang Y.
europepmc +1 more source
A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance
Annals of Clinical and Translational Neurology, EarlyView.ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley +1 more source
Delineating Intellectuals and Social Conscience
, 2009 知识分子总是存在如何对待社会和怎样自我对待的问题。以体现“社会良知“、承载人类价值作为知识分子的特性的观点,是对这两个问题的一种有代表性的回答。但是,知识分子并不必定承载社会良知,也并非只有知识分子才具备“价值自觉“,而一旦知识分子以行动而非纯粹的话语方式来展现自己的价值自觉,将可能导致知识分子的错位甚至自我否定。Intellectuals must always confront the problems of how to treat the society and how to treat ...
李琦
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Ein Fenster zur Welt. Osteuropa in der "New York Review of Books", 1963-2003
Zeitschrift für Ostmitteleuropa-Forschung, 2020 Victoria Harms
doaj +1 more source