Results 121 to 130 of about 2,524,574 (309)

Fluid Biomarkers of Disease Burden and Cognitive Dysfunction in Progressive Supranuclear Palsy

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Identifying objective biomarkers for progressive supranuclear palsy (PSP) is crucial to improving diagnosis and establishing clinical trial and treatment endpoints. This study evaluated fluid biomarkers in PSP versus controls and their associations with regional 18F‐PI‐2620 tau‐PET, clinical, and cognitive outcomes.
Roxane Dilcher   +10 more
wiley   +1 more source

Navigating visa inequities: mobility as privilege in academia - 'You are not supposed to be here'

open access: yesGlobal Social Challenges Journal
This provocation critically examines the unequal terrain of academic mobility, its impact on knowledge production and on who has the right to be an agent of scientific knowledge. Drawing on personal experiences of more than 15 years (autoethnography) and
Devran Gülel
doaj   +1 more source

Cross-Disciplinary Rapid Scoping Review of Structural Racial and Caste Discrimination Associated with Population Health Disparities in the 21st Century

open access: yesSocieties
A cross-disciplinary rapid scoping review was carried out, generally following the PRISMA-SCR protocol to examine historical racial and caste-based discrimination as structural determinants of health disparities in the 21st century.
Drona P. Rasali   +7 more
doaj   +1 more source

Comparing Race and Sex Discrimination in Custody Cases [PDF]

open access: yes, 1999
In her article Prof. Bartlett focuses on race and sex, not where they cross, but what they look like side by side using child custody as a starting point for a more detailed assessment of the similarities and differences between sex and race ...
Bartlett, Katharine T.
core   +2 more sources

Structure–Function Decoupling of the Sensorimotor and Default Mode Networks in Black Americans With MS

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Multiple sclerosis (MS) exhibits racially disparate rates of disease progression. Black people with MS (B‐PwMS) experience a more severe disease course than non‐Hispanic White people with MS (NHW‐PwMS). Here we investigated structural and functional connectivity as well as structure–function decoupling in the ...
Emilio Cipriano   +11 more
wiley   +1 more source

Mitigating Bias Due to Race and Gender in Machine Learning Predictions of Traffic Stop Outcomes

open access: yesInformation
Traffic stops represent a crucial point of interaction between citizens and law enforcement, with potential implications for bias and discrimination.
Kevin Saville   +2 more
doaj   +1 more source

Forms of Discrimination [PDF]

open access: yes, 2001
Fact sheet on various forms of discrimination in the workplace, prepared by the ...
InFocus Programme on Promoting the Declaration on Fundamental Principles and Rights at Work   +1 more
core   +1 more source

Complementarity of Long‐Reads and Optical Mapping in Parkinson's Disease for Structural Variants

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Long‐read sequencing and optical genome mapping technologies have the ability to detect large and complex structural variants. This has led to the discovery of novel pathogenic variants in neurodegenerative movement disorders. Thus, we aimed to systematically compare the SV detection capabilities of OGM and ONT in Parkinson's disease.
André Fienemann   +17 more
wiley   +1 more source

University Students’ Views on the Challenges Faced by Students with Difficulties

open access: yesSocial Sciences
Introduction: The pursuit of an inclusive university is rooted in the commitment to ensuring equal opportunities within the educational landscape.
Sonia Ruiz de Azua   +4 more
doaj   +1 more source

Epilepsy‐Associated Variants of a Single SCN1A Codon Exhibit Divergent Functional Properties

open access: yesAnnals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Pathogenic variants in SCN1A, which encodes the voltage‐gated sodium channel NaV1.1, are associated with multiple epilepsy syndromes exhibiting a range of clinical severity. SCN1A variants are reported in different syndromes, including Dravet syndrome, which is associated with loss‐of‐function, whereas neonatal/infantile‐onset ...
Lanie N. Liebovitz   +3 more
wiley   +1 more source

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