Results 121 to 130 of about 279,319 (265)

Testing certain and uncertain incentives on study retention in a longitudinal social media survey among young adults: An embedded recruitment trial

Digital Health
Introduction Incentives can be effective in survey research but evidence is limited on how incentive type impacts survey retention in longitudinal social media-based surveys. This study examined how certain and uncertain incentives affect study retention
Jennifer Cantrell, Megumi Ichimiya, Paul Mowery, Alexander P D’Esterre, Jeffrey Bingenheimer, Shreya Tulsiani, Elizabeth C Hair, Jennifer M Kreslake, Madeline Martin, Raquel Gerard, William Douglas Evans   +10 more
doaj   +1 more source

George E.S. Boley, Part 1

, 2009
Location: MontserradoRuntime: 0:07:39Categorized as pertaining to Diaspora, Hearings.The Truth and Reconciliation Commission of ...
George E.S. Boley
core  

GAD65 Antibody ELISA With Extended Reportable Range: Validation and Guidance for Neurological Practice

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To (1) validate GAD65‐ELISA detection and quantification for type 1 diabetes mellitus and autoimmune neurological diagnoses, (2) correlate ELISA results (reference range < 5 IU/mL) with established radioimmunoprecipitation assay (RIA; ≤ 0.02 nmol/L), and (3) define ELISA clinical utility and pitfalls.
Andrew McKeon, Dana Olofson, Diana Anissian, Divyanshu Dubey, Eoin P. Flanagan, Max C. Herman, Sarosh R. Irani, Daniel H. Lachance, Maria A. Willrich, Sean Pittock, John R. Mills, Anastasia Zekeridou   +11 more
wiley   +1 more source

Francis Dolo, Part 2

, 2009
Location: MontserradoRuntime: 1:22:52Categorized as pertaining to Diaspora, Hearings.The Truth and Reconciliation Commission of ...
Francis Dolo
core  

RNA Sequencing Resolves Cryptic Pathogenic Variants in Mitochondrial Disease

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Mitochondrial diseases are the most common inherited metabolic disorders, characterized by pronounced clinical and genetic heterogeneity that complicates molecular diagnosis. Although DNA‐based sequencing approaches have become standard in genetic testing, up to half of patients remain without a definitive diagnosis.
Zhimei Liu, Xin Duan, Fatemeh Peymani, Jia Wang, Chengjia Bao, Chaolong Xu, Ying Zou, Zixuan Zhang, Yunxi Zhang, Tongyue Li, Martin Pavlov, Junling Wang, Minhan Song, Tianyu Song, Xiaodi Han, Mingxi Sun, Danmin Shen, Ruoyu Duan, Huafang Jiang, Manting Xu, Holger Prokisch, Fang Fang   +21 more
wiley   +1 more source

Confronting Confederate Monuments: Place-Based Pedagogy for Anti-Racist Preaching

Religions
“Space wins” is a long-held homiletical maxim. Usually, this means that architecture and pulpit style influence how sermons are delivered and heard. What is less frequently considered is how monuments and memorials affect proclamation in space.
David M. Stark
doaj   +1 more source

Pajibo Kyne, Witness Testimony, Part 3

, 2008
Categorized as pertaining to Diaspora, Hearings.Location: Hamline University; St.
Kyne, Pajibo
core  

White Matter Hyperintensity Burden and Short‐Interval Change Associated With Sleep Apnoea in the UK Biobank

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Purpose White matter hyperintensities (WMH) are a core neuroimaging marker of cerebral small vessel disease (CSVD). Sleep apnoea (SA) is a recognized vascular risk factor, but its associations with regional WMH burden, short‐interval WMH change and cognitive performance in population‐based cohorts remain incompletely defined. We
Peng Cheng, Diego Z. Carvalho, Shahid Karim, Anwar Chahal, Virend K. Somers   +4 more
wiley   +1 more source

Lewis G. Brown, Part 3

, 2008
Location: MontserradoRuntime: 4:46:36Hearing Type: Institutional and ThematicCategorized as pertaining to Diaspora, Hearings.The Truth and Reconciliation Commission of ...
Lewis G. Brown
core  

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source