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2 result(s) for 'author#Inga Sophia Knoth' within BMC

1. Steady-state visual evoked potentials in children with neurofibromatosis type 1: associations with behavioral rating scales and impact of psychostimulant medication

   Neurofibromatosis type 1 (NF1) is a genetic disorder often associated with cognitive dysfunctions, including a high occurrence of deficits in visuoperceptual skills. The neural underpinnings of these visuoperc...

   Authors: Eve Lalancette, Audrey-Rose Charlebois-Poirier, Kristian Agbogba, Inga Sophia Knoth, Emily J. H. Jones, Luke Mason, Sébastien Perreault and Sarah Lippé

   Citation: Journal of Neurodevelopmental Disorders 2022 14:42

   Content type: Research Published on: 22 July 2022

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2. Auditory repetition suppression alterations in relation to cognitive functioning in fragile X syndrome: a combined EEG and machine learning approach

   Fragile X syndrome (FXS) is a neurodevelopmental genetic disorder causing cognitive and behavioural deficits. Repetition suppression (RS), a learning phenomenon in which stimulus repetitions result in diminish...

   Authors: Inga Sophia Knoth, Tarek Lajnef, Simon Rigoulot, Karine Lacourse, Phetsamone Vannasing, Jacques L. Michaud, Sébastien Jacquemont, Philippe Major, Karim Jerbi and Sarah Lippé

   Citation: Journal of Neurodevelopmental Disorders 2018 10:4

   Content type: Research Published on: 29 January 2018

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