Results 241 to 250 of about 9,120,288 (390)
The Aesthetic and Political Practices of East-Central European Music Videos after 2000 (dataset)
Tomáš Jirsa
openalex +1 more source
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
ABSTRACT Objective Rett syndrome (RTT) is a devastating neurodevelopmental disorder with developmental regression affecting motor, sensory, and cognitive functions. Sensory disruptions contribute to the complex behavioral and cognitive difficulties and represent an important target for therapeutic interventions.
Alex Joseph Simon +12 more
wiley +1 more source
Genome sequence of a human monkeypox virus isolate from Central Europe during the 2022 outbreak. [PDF]
Nagy ÁG +8 more
europepmc +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
Scuttle flies (Diptera, Phoridae) collected by mosquito trap from Košice Zoo, Central Europe. [PDF]
Grundmann B +5 more
europepmc +1 more source
Cereal Agriculture in Prehistoric North-Central Europe and South-East Iberia: Changes and Continuities as Potential Adaptations to Climate [PDF]
Julien Schirrmacher +5 more
openalex +1 more source
ABSTRACT Objective Facioscapulohumeral muscular dystrophy type 1 (FSHD1) is a progressive neuromuscular disorder with no approved treatments. Identifying reliable biomarkers is critical to monitor disease severity, activity, and progression. Interleukin‐6 (IL‐6) has been proposed as a candidate biomarker, but longitudinal validation is limited ...
Jonathan Pini +13 more
wiley +1 more source
One Century of Change: Stronger Diversity Decline in Lowland Than in Mountain Grasslands in Central Europe. [PDF]
Widmer S +6 more
europepmc +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
ABSTRACT Objective SNUPN‐related muscular dystrophy or LGMDR29 is a new entity that covers from a congenital or childhood onset pure muscular dystrophy to more complex phenotypes combining neurodevelopmental features, cataracts, or spinocerebellar ataxia. So far, 12 different variants have been described.
Nuria Muelas +18 more
wiley +1 more source

