Results 131 to 140 of about 863,191 (328)
Visual Recovery Reflects Cortical MeCP2 Sensitivity in Rett Syndrome
Annals of Clinical and Translational Neurology, EarlyView.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
Koncept dětské abnormality v 19. století
Theatrum Historiae, 2013 The article deals with the perception of the abnormality of children in 19.th century. The first part concerns the theoretical view of enlightenment and the view of philanthropists and the searching of the causes of abnormality.
Martina Halířová
doaj
Characteristics of neurological Wilson’s disease with corpus callosum abnormalities [PDF]
, 2019 Zhihua Zhou +8 more
openalex +1 more source
Skull Abnormalities in Cadavers in the Gross Anatomy Lab [PDF]
, 2020 Jessica De Rose +2 more
openalex +1 more source
Abnormal neurobiochemical metabolites in the first- episode schizophrenia and clinical high-risk population. [PDF]
, 2021 Lijun Ouyang +5 more
openalex +1 more source
Annals of Clinical and Translational Neurology, EarlyView.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
Annals of Clinical and Translational Neurology, EarlyView.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
Regional Homogeneity Abnormalities in Early-Onset and Adolescent-Onset Conduct Disorder in Boys: A Resting-State fMRI Study [PDF]
, 2019 Wanyi Cao +7 more
openalex +1 more source
SNUPN‐Related Muscular Dystrophy: Novel Phenotypic, Pathological and Functional Protein Insights
Annals of Clinical and Translational Neurology, EarlyView.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
Computer Vision and Abnormal Patient Gait: A Comparison of Methods [PDF]
, 2020 Jasmin Hundal, Benson A. Babu
openalex +1 more source