Results 101 to 110 of about 1,851,054 (308)
The contribution of an events programme to sustainable heritage conservation: a study of the National Trust in England. [PDF]
Whilst for many nations progressing a sustainable development agenda is a priority, for others, conserving their existing socio-natural heritage in a sustainable way may be significant. In the United Kingdom, the National Trust, a charitable organisation,
Fox, Dorothy, Johnston, Nicky
core
New observables for multiple-parton interactions measurements using Z + jets process at the LHC
Multiple-parton interactions play a vital role in hadron-hadron collisions. This paper presents a study of the multiple-parton interactions with simulated Z + jets events in proton-proton collisions at a centre-of-mass energy of 13 TeV.
Bansal, M. +3 more
core +1 more source
Practice Recommendations for Genetic Testing of Ataxias
ABSTRACT Objective Over the past decade, significant advances in genetic testing for ataxia have improved diagnostic accuracy, informed clinical trial eligibility, guided treatment decisions, and enabled cascade testing of at‐risk relatives. While guidance exists for other neurogenetic conditions, there are no standardized guidelines on genetic ...
Sharan R. Srinivasan +7 more
wiley +1 more source
Introduction As part of the Alberta Health Services (AHS) Calgary Zone Healthcare planning, a Palliative and End of Life Care Program (PEOLC) dashboard was developed and face validity of the indicators was examined by key stakeholders such as clinicians ...
Pin Cai +2 more
doaj +1 more source
Debating critical costume: negotiating ideologies of appearance, performance and disciplinarity [PDF]
In this article, I present an argument for a proposed focus of ‘critical costume’. Critical Costume, as a research platform, was founded in 2013 to promote new debate and scholarship on the status of costume in contemporary art and culture.
Hann, Rachel
core +2 more sources
ABSTRACT Objective Paroxysmal kinesigenic dyskinesia (PKD) is the most common hereditary paroxysmal movement disorder. The PRRT2 gene is the first identified causative gene and accounts for the majority of PKD. In this study, we investigated the pathogenicity of PRRT2 variants in the splice regions. Methods Patients with clinically suspected PKD and no
Jiao‐Jiao Xu +5 more
wiley +1 more source
Gender differences in survival across the ages of life: an introduction
This thematic series explores the complex nature of the survival gap between genders across the lifespan. It highlights how, although women generally have a longer life expectancy than men globally, the complexity of this advantage challenges simplistic ...
Virginia Zarulli, Giambattista Salinari
doaj +1 more source
Which best predicts suicides in Northern Ireland - self-rated mental health or medication record?
Background Over 800,000 suicides occur annually worldwide, and approximately 300 suicides in Northern Ireland (NI) each year. Studies from elsewhere have highlighted the role of mental health in the risk of death by suicide, but such studies are scarce ...
Ifeoma Onyeka +2 more
doaj +1 more source
INF2‐Related Charcot–Marie–Tooth Disease in a Japanese Cohort: Genetic and Clinical Insights
ABSTRACT Background INF2 mutations cause focal segmental glomerulosclerosis (FSGS) and Charcot–Marie–Tooth disease (CMT). Accurate genetic diagnosis is critical, as INF2‐related FSGS is typically resistant to immunotherapy yet rarely recurs after transplantation, and its associated neuropathy can mimic treatable immune‐mediated disorders such as ...
Chikashi Yano +27 more
wiley +1 more source
The politics of administrative data: A case study of school census data for children with SEND
Background From 2016 to 2018 we collaborated on a programme of work with a local authority in the South West of England around understanding diagnosis trends for children with special educational needs and disabilities (SEND).
Emily Rempel +2 more
doaj +1 more source

