This content links with Goal 3: Good health and well-being and Goal 10: Reduced Inequalities by providing insights into progressive supranuclear palsy (PSP), a neurodegenerative disorder pathologically characterized by accumulation of abnormal tau protein in subcortical nuclei neurons forming the neurofibrillary tangles, and in glial cells as tufted astrocytes and oligodendroglial inclusions.
The Lancet Neurology, Volume 21, Issue 11, November 2022, Pages 1004-1060,
This update to the 2017 Lancet Neurology Commission on traumatic brain injury advances SDG 3 by presenting new insights and challenges across a range of topics around traumatic brain injury, a leading cause of injury-related death and disability worldwide, with devastating effects on patients and their families.
Elsevier,
Research Ethics in Behavior Analysis: From Laboratory to Clinic and Classroom, 2023, Pages 63-86
This chapter advances the UN SDG Goal 3: Good Health and Goal 10: Reduced Inequalities by discussing the importance of equity, diversity, inclusion, and accessibility (EDIA) as related to research in applied behavior analysis.
This article explores health disparities based on the intersection of sex, geography, race, and ethnicity that have been identified for poorer pre- and postnatal outcomes in the general population, as well as those with critical congenital heart disease.
To help create awareness and observe the International Day of Persons with Disabilities (IDPD) on 3 December 2022, Elsevier is proud to showcase a special issue of freely available journal articles and book chapters to share.
This Editorial highlights 17 contributions from outstanding women researchers in chemical engineering supporting SDG 5 (Gender equality) as well as SDG 9 (Industry, innovation and infrastructure).
This Study supports SDGs 3, 5 and 10, investigating the impact of chemotherapy on the immune system of older women with breast cancer.
Based on current studies, the incidence of Ewing sarcoma (ES) varies significantly by race and ethnicity, with the disease being most common in patients of European ancestry. However, race/ethnicity has generally been self-reported rather than formally evaluated at a population level using DNA evidence. Additionally, mitochondrial dysfunction is a hallmark of ES, yet there have been no reported studies of mitochondrial genetics in ES. Thus, we evaluated both the mitochondrial and nuclear ancestries of 420 pediatric ES patients in the United States using whole-genome sequencing.
The Lancet Global Health, available online 11 October 2022, in press.
An Article in support of SDGs 3, 5, and 10, showing that effective cataract surgical coverage varies widely between countries, increases with greater income level, and is higher in men.
