Results 131 to 140 of about 7,508 (277)
Urban public health emergencies and the COVID-19 pandemic. Part 1: Social and spatial inequalities in the COVID-city. [PDF]
Orford S, Fan Y, Hubbard P.
europepmc +1 more source
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
Picnic methodology: rethinking multispecies relationships through alfresco meals [PDF]
Kaisu Koski
openalex +1 more source
ABSTRACT Objective Cognitive impairment, fatigue, and depression are common in multiple sclerosis (MS), potentially due to disruption of regional functional connectivity caused by white matter (WM) lesions. We explored whether WM lesions functionally connected to specific brain regions contribute to these MS‐related manifestations.
Alessandro Franceschini+7 more
wiley +1 more source
Kontextstyrd heuristik : användbarhetsutvärdering av Alfresco
Syftet med detta examensarbete att undersöka om systemsuiten Alfresco uppfyller krav på användbarhet för dokumenthantering och samarbete i interaktiva miljöer. Vidare är syftet att analysera om heuristisk utvärdering en lämplig utvärderingsmetod för konsultbolag att använda sig av vid utvärdering av olika systemalternativ för dokumenthantering då kund ...
openaire +1 more source
Impact of a complex gender-transformative intervention on maternal and child health outcomes in the eastern Democratic Republic of Congo: protocol of a longitudinal parallel mixed-methods study. [PDF]
Bapolisi WA+6 more
europepmc +1 more source
Vitamin D Deficiency and Its Associated Factors among Female Migrants in the United Arab Emirates. [PDF]
Anouti FA+7 more
europepmc +1 more source
ABSTRACT Objective Natalizumab (NTZ) is a highly effective therapy for multiple sclerosis (MS); however, its use is limited by the risk of a rare potentially severe opportunistic brain infection, progressive multifocal leukoencephalopathy (PML). Alternative dosing strategies are evaluated to reduce PML risk while still maintaining efficacy, which ...
Regina Berkovich+10 more
wiley +1 more source
ABSTRACT Objective Alexander disease (AxD) is a severe neurodegenerative disorder caused by gain‐of‐function mutations in the gene for GFAP, which lead to protein aggregation and a primary astrocytopathy. Symptoms vary, but failure to thrive (FTT) and frequent emesis are common and cause significant morbidity. Here we investigate GDF15, a member of the
Tracy L. Hagemann+6 more
wiley +1 more source
ABSTRACT Introduction Neuronal pentraxin 2 (NPTX2) is a synaptic protein involved in synaptic plasticity and regulation of neuronal excitability. Lower baseline cerebrospinal fluid (CSF) NPTX2 levels have been shown to be associated with an earlier onset of mild cognitive impairment (MCI), a pre‐dementia syndrome, even after CSF Alzheimer's Disease (AD)
Juan P. Vazquez+12 more
wiley +1 more source