Results 51 to 60 of about 173,609 (136)
Novel E815K knock-in mouse model of alternating hemiplegia of childhood
De novo mutations causing dysfunction of the ATP1A3 gene, which encodes the α3 subunit of Na+/K+-ATPase pump expressed in neurons, result in alternating hemiplegia of childhood (AHC).
Ashley R. Helseth +11 more
doaj +1 more source
Gait Alterations Due to DCC Gene Variants in Individuals with Congenital Mirror Movements
Abstract Background Congenital Mirror Movement Syndrome (CMMS) involves involuntary movements on one side of the body while voluntary movements are performed on the other side. They disrupt left–right coordination and can be caused by a pathogenic variant in the DCC gene.
Nok‐Yeung Law +7 more
wiley +1 more source
ABSTRACT Introduction Although whole‐body vibration (WBV) therapy has already demonstrated efficacy in improving lower‐limb muscle strength, it is still unclear whether it has similar potential for improving handgrip strength. Objective To verify the efficacy of WBV on handgrip strength. Methods The search was conducted on September 5, 2025, in PubMed,
Julien Dines Labarrere +5 more
wiley +1 more source
ATP1A3 mutations and genotype-phenotype correlation of alternating hemiplegia of childhood in Chinese patients. [PDF]
Alternating hemiplegia of childhood (AHC) is a rare and severe neurological disorder. ATP1A3 was recently identified as the causative gene. Here we report the first genetic study in Chinese AHC cohort.
Xiaoling Yang +7 more
doaj +1 more source
ABSTRACT Real‐time monitoring of subtle muscle deformation remains of considerable importance for cooperative human‐exoskeleton control. Highly integrated flexible triboelectric nanogenerators (TENGs), owing to their self‐powered operation and high sensing resolution, are well suited for continuous physiological monitoring and human‐robot interaction ...
Heran Li +9 more
wiley +1 more source
Abstract Background Previous studies on calcium channel blockers (CCBs) and Parkinson's disease (PD) risk reached conflicting conclusions. Objectives We examined the relationship between CCBs and PD in the E3N cohort of French women followed for 15 years (2004–2018), while taking into account the potential for reverse causation.
Emilie Moutard +9 more
wiley +1 more source
This cross‐sectional study reports on the content and construct validity of the Both Hands Assessment (BoHA) for measuring bimanual performance in children and adolescents with bilateral cerebral palsy (MACS levels I–III), aged 18 months to 18 years. Abstract Aim To investigate the content and construct validity of the Both Hands Assessment (BoHA) for ...
Gøril Okkenhaug Johansen +5 more
wiley +1 more source
Abstract Background Staphylococcus lugdunensis is a coagulase‐negative Staphylococcus that has been increasingly recognised as a significant pathogen capable of causing invasive infections similar to Staphylococcus aureus. Data comparing the clinical manifestations and outcomes of S. lugdunensis bacteraemia to S. aureus bacteraemia remain limited. This
Gemma Webb +5 more
wiley +1 more source
Alternating hemiplegia of childhood: New diagnostic options [PDF]
A syndrome of alternating hemiplegia of childhood (AHC) is a rare disorder first presented in 1971. AHC is characterized by transient episodes of hemiplegia affecting either one or both sides of the body.
Gergont, Aleksandra; Department of Neurology of Children and Youth, Jagiellonian University, Collegium Medicum, Krakow, Poland +1 more
core +1 more source
Brain–Computer Interfaces: The Dawn of a New Era in Disease Treatment
This study investigates the potential of brain–computer interface (BCI) technology in treating neuropsychiatric disorders, such as movement and communication barriers. Our review examines the history, signal paradigms, and diverse applications of BCI while also discussing ongoing research into novel materials and emerging technologies that offer ...
Yuqi Feng +11 more
wiley +1 more source

