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Kai Eriksson

Showing results (21-30 of 39) with videos related to

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Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 19, 2014
EEG, evoked potentials and pulsed Doppler in asphyxiated term infantsMia K Julkunen, Sari-Leena Himanen, Kai Eriksson, et al.
Epilepsy & Behavior : E&B|October 20, 2006
The effects of valproate exposure in utero on behavior and the need for educational support in school-aged childrenKatriina Viinikainen, Kai Eriksson, Anne Mönkkönen, et al.
Epilepsy Research|July 21, 2005
Children exposed to valproate in utero--population based evaluation of risks and confounding factors for long-term neurocognitive developmentKai Eriksson, Katriina Viinikainen, Anne Mönkkönen, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 1, 2017
Atypical physiological orienting to direct gaze in low-functioning children with autism spectrum disorderTerhi M Helminen, Jukka M Leppänen, Kai Eriksson, et al.
Epilepsia|April 14, 2007
Social functioning and psychological well-being of 347 young adults with epilepsy only--population-based, controlled study from FinlandAnne Koponen, Ullamaija Seppälä, Kai Eriksson, et al.
Epilepsy Research|October 21, 2017
The incidence and risk factors of epilepsy in children born preterm: A nationwide register studyMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Pediatrics|July 19, 2018
Visual and Hearing Impairments After Preterm BirthMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Pediatrics|November 26, 2014
Cerebral palsy among children born moderately and late pretermMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Journal of Autism and Developmental Disorders|May 25, 2019
Atypical Pattern of Frontal EEG Asymmetry for Direct Gaze in Young Children with Autism Spectrum DisorderJenni Lauttia, Terhi M Helminen, Jukka M Leppänen, et al.
Neuro-Degenerative Diseases|July 16, 2011
Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB genePäivi Koskenkorva, Jelena Hyppönen, Marja Aikiä, et al.
Pageof 4

Showing results (21-30 of 39) with videos related to

Sort By:
Pageof 4
Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|February 19, 2014
EEG, evoked potentials and pulsed Doppler in asphyxiated term infantsMia K Julkunen, Sari-Leena Himanen, Kai Eriksson, et al.
Epilepsy & Behavior : E&B|October 20, 2006
The effects of valproate exposure in utero on behavior and the need for educational support in school-aged childrenKatriina Viinikainen, Kai Eriksson, Anne Mönkkönen, et al.
Epilepsy Research|July 21, 2005
Children exposed to valproate in utero--population based evaluation of risks and confounding factors for long-term neurocognitive developmentKai Eriksson, Katriina Viinikainen, Anne Mönkkönen, et al.
Autism Research : Official Journal of the International Society for Autism Research|March 1, 2017
Atypical physiological orienting to direct gaze in low-functioning children with autism spectrum disorderTerhi M Helminen, Jukka M Leppänen, Kai Eriksson, et al.
Epilepsia|April 14, 2007
Social functioning and psychological well-being of 347 young adults with epilepsy only--population-based, controlled study from FinlandAnne Koponen, Ullamaija Seppälä, Kai Eriksson, et al.
Epilepsy Research|October 21, 2017
The incidence and risk factors of epilepsy in children born preterm: A nationwide register studyMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Pediatrics|July 19, 2018
Visual and Hearing Impairments After Preterm BirthMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Pediatrics|November 26, 2014
Cerebral palsy among children born moderately and late pretermMikko Hirvonen, Riitta Ojala, Päivi Korhonen, et al.
Journal of Autism and Developmental Disorders|May 25, 2019
Atypical Pattern of Frontal EEG Asymmetry for Direct Gaze in Young Children with Autism Spectrum DisorderJenni Lauttia, Terhi M Helminen, Jukka M Leppänen, et al.
Neuro-Degenerative Diseases|July 16, 2011
Severer phenotype in Unverricht-Lundborg disease (EPM1) patients compound heterozygous for the dodecamer repeat expansion and the c.202C>T mutation in the CSTB genePäivi Koskenkorva, Jelena Hyppönen, Marja Aikiä, et al.
Pageof 4