Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Lore, Wyers"'
Publikováno v:
Journal of the Peripheral Nervous System. 28:79-85
Rare life-threatening conditions, such as multisystemic hereditary transthyretin amyloidosis (ATTRv) polyneuropathy, are often underdiagnosed or diagnosed late in the disease course, although early diagnosis is crucial for treatment success. Red flag
Autor:
Karen Verheyen, Lore Wyers, Eugénie Lambrecht, An‐Sofie Schoonjans, Berten Ceulemans, Patricia van de Walle, Ann Hallemans
Publikováno v:
Developmental medicine and child neurology
AimThis cohort study aimed to describe functional mobility in Dravet syndrome, a developmental and epileptic encephalopathy. MethodFunctional mobility was assessed in individuals (aged 3-25 years), diagnosed with Dravet syndrome, using the Functional
Autor:
George F. Wittenberg, Ilse Jonkers, Stephan P. Swinnen, Nick Kortzorg, Gina McKernan, Charles W. Lafe, Jing Tian, Oron Levin, Lore Wyers, Florian Van Halewyck, Matthieu P. Boisgontier, M. A. Urbin
Publikováno v:
Experimental Brain Research. 239:3585-3600
Contributions from premotor and supplementary motor areas to reaching behavior in aging humans are not well understood. The objective of these experiments was to examine effects of perturbations to specific cortical areas on the control of unconstrai
Autor:
Patricia Van de Walle, Ann Hallemans, An-Sofie Schoonjans, Berten Ceulemans, Lore Wyers, Karen Verheyen, Alessandra Del Felice
Publikováno v:
Developmental medicine and child neurology
To investigate the relation between cognitive and motor development in preschool aged children with Dravet syndrome, in particular between the age of independent walking and cognitive development.Results of cognitive and motor developmental assessmen
Autor:
George F. Wittenberg, Jing Tian, Nick Kortzorg, Lore Wyers, Florian Van Halewyck, Matthieu P. Boisgontier, Oron Levin, Stephan P. Swinnen, Ilse Jonkers
Publikováno v:
Exp Brain Res
Reaching for an object in space forms the basis for many activities of daily living and is important in rehabilitation after stroke and in other neurological and orthopedic conditions. It has been the object of motor control and neuroscience research
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f88359029b417766ab9c18f536d466b
https://europepmc.org/articles/PMC9985825/
https://europepmc.org/articles/PMC9985825/
Autor:
P. Van de Walle, Kaat Desloovere, Lore Wyers, Ann Hallemans, Berten Ceulemans, A-S. Schoonjans, Karen Verheyen
Publikováno v:
Gait and posture
BACKGROUND: Clinical laboratory testing of locomotor disorders is challenging in patients with intellectual disability (ID). Nevertheless, also in this population gait analysis has substantial value as motor problems are common. To promote its use, a
Autor:
Ann Hallemans, P. Van de Walle, Karen Verheyen, An-Sofie Schoonjans, Berten Ceulemans, Lore Wyers
Publikováno v:
Gait & Posture. 90:298-299
Autor:
M A, Urbin, Jing, Tian, Charles W, Lafe, Gina P, McKernan, Nick, Kortzorg, Lore, Wyers, Florian, Van Halewyck, Matthieu P, Boisgontier, Oron, Levin, Stephan P, Swinnen, Ilse, Jonkers, George F, Wittenberg
Publikováno v:
Experimental brain research. 239(12)
Contributions from premotor and supplementary motor areas to reaching behavior in aging humans are not well understood. The objective of these experiments was to examine effects of perturbations to specific cortical areas on the control of unconstrai
Autor:
Karen Verheyen, Kaat Desloovere, Ann Hallemans, Lore Wyers, An-Sofie Schoonjans, Patricia Van de Walle, Berten Ceulemans
Publikováno v:
European journal of paediatric neurology
Background: Dravet Syndrome (DS) is a developmental and epileptic encephalopathy, characterized by drug resistant infantile onset seizures and cognitive and motor impairment. Walking problems progressively occur and crouch gait is frequently observed
Autor:
Ann Hallemans, An-Sofie Schoonjans, Berten Ceulemans, Kaat Desloovere, Patricia Van de Walle, Karen Verheyen, Lore Wyers
Publikováno v:
Gait and posture
Background Dravet Syndrome (DS) is a developmental and epileptic encephalopathy starting in infancy and characterised by treatment resistant epilepsy with cognitive impairment and progressive motor dysfunction. Walking becomes markedly impaired with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57880bf93431d10c2d11c72a4c72afc1
https://lirias.kuleuven.be/handle/123456789/668115
https://lirias.kuleuven.be/handle/123456789/668115