Results 141 to 150 of about 41,572 (277)

Somato‐Cognitive Action Network in Focal Dystonia

open access: yesMovement Disorders, EarlyView.
Abstract Background The central pathology causing idiopathic focal dystonia remains unclear. The recently identified somato‐cognitive action network (SCAN) has been implicated. Objective We tested whether the effector‐agnostic SCAN may constitute a central pathology shared across dystonia subtypes, whereas the effector‐specific regions in the primary ...
Yuchao Wang   +8 more
wiley   +1 more source

Hand, Foot, and Mouth Disease

open access: yes, 1964
J. M. Brown, John A. Wright, W. S. Ogden
semanticscholar   +1 more source

RRP12 Variants Are Associated With Autosomal Recessive Brain Calcifications

open access: yesMovement Disorders, EarlyView.
Abstract Background Primary brain calcifications are observed in several inherited diseases due to different pathogenic mechanisms, including the disruption of the neurovascular unit, mitochondrial dysfunction, and impaired nucleic acid metabolism.
Edoardo Monfrini   +19 more
wiley   +1 more source

An atypical winter outbreak of hand, foot, and mouth disease associated with human enterovirus 71, 2010 [PDF]

open access: gold, 2014
Nan Liu   +13 more
openalex   +1 more source

Epidemiological characteristics, routine laboratory diagnosis, clinical signs and risk factors for hand, -foot -and -mouth disease: A systematic review and meta-analysis

open access: gold, 2022
Zhijie Yi   +11 more
openalex   +2 more sources

Rare but Relevant? Assessing Variants in Dystonia‐Linked Genes in Parkinson's Disease

open access: yesMovement Disorders, EarlyView.
Abstract Background Dystonia and Parkinson's disease (PD) exhibit clinical and genetic overlap, but the relevance of dystonia gene variants in PD remains unclear. Objective The aim was to assess the frequency of dystonia‐linked pathogenic variants in PD.
Lara M. Lange   +37 more
wiley   +1 more source

Hand, foot and mouth disease caused by Coxsackie viruses A6 and A16 in Assam, Northeast India: A need for surveillance

open access: diamond, 2019
Biswajyoti Borkakoty   +6 more
openalex   +1 more source

Expanding the Genetic and Phenotypic Spectrum of DYT‐VPS16: The Importance of Splice‐Site Variants

open access: yesMovement Disorders, EarlyView.
Abstract Background DYT‐VPS16, an early‐onset isolated dystonia caused by variants in the VPS16 gene, has been reported in fewer than 70 patients. Methods We explored the clinical and genotypic spectrum of DYT‐VPS16 by investigating early‐onset dystonia patients with VPS16 variants discovered in our large Biodatabank and through gene‐matching ...
Ana Westenberger   +39 more
wiley   +1 more source

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