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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 9, 2009
Alexander disease: early presence of cerebral MRI criteria
Claudia B Poloni, Solène Ferey, Charles-Antoine Haenggeli, et al.
Epilepsy Research
|
December 18, 2019
Localizing non-epileptiform abnormal brain function in children using high density EEG: Electric Source Imaging of focal slowing
Sara Baldini, Ana Coito, Christian M Korff, et al.
Epilepsy Research
|
December 10, 2013
Localization of the epileptogenic tuber with electric source imaging in patients with tuberous sclerosis
Odysseas Kargiotis, Agustina M Lascano, Valentina Garibotto, et al.
Archives of Neurology
|
August 10, 2011
Encephalitis associated with glutamic acid decarboxylase autoantibodies in a child: a treatable condition?
Christian M Korff, Paloma Parvex, Laurent Cimasoni, et al.
Scientific Data
|
August 16, 2025
High-Density EEG Source Localisation of averaged interictal epileptic Discharges validated by surgical Outcome
Bernd J Vorderwülbecke, Margherita Carboni, Sebastien Tourbier, et al.
Cells
|
October 27, 2023
Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing <i>GNAO1</i> Mutation P170R
Yonika A Larasati, Gonzalo P Solis, Alexey Koval, et al.
Epilepsy Research
|
April 1, 2014
When is a child with status epilepticus likely to have Dravet syndrome?
François Le Gal, Sébastien Lebon, Gian Paolo Ramelli, et al.
Medcomm
|
May 8, 2025
Novel Mutation at Cys225 in <i>GNAO1</i>-Associated Developmental and Epileptic Encephalopathies: Clinical, Molecular, and Pharmacological Profiling of Case Studies
Yonika A Larasati, Gonzalo P Solis, Alexey Koval, et al.
American Journal of Medical Genetics. Part A
|
June 21, 2017
SERPINI1 pathogenic variants: An emerging cause of childhood-onset progressive myoclonic epilepsy
Emmanuelle Ranza, Stephanie Garcia-Tarodo, Konstantinos Varvagiannis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 24, 2014
When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?
Sébastien Lebon, Philippe Suarez, Semsa Alija, et al.
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Search research articles
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Showing results (61-70 of 83) with videos related to
Sort By:
Page
of 9
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
January 9, 2009
Alexander disease: early presence of cerebral MRI criteria
Claudia B Poloni, Solène Ferey, Charles-Antoine Haenggeli, et al.
Epilepsy Research
|
December 18, 2019
Localizing non-epileptiform abnormal brain function in children using high density EEG: Electric Source Imaging of focal slowing
Sara Baldini, Ana Coito, Christian M Korff, et al.
Epilepsy Research
|
December 10, 2013
Localization of the epileptogenic tuber with electric source imaging in patients with tuberous sclerosis
Odysseas Kargiotis, Agustina M Lascano, Valentina Garibotto, et al.
Archives of Neurology
|
August 10, 2011
Encephalitis associated with glutamic acid decarboxylase autoantibodies in a child: a treatable condition?
Christian M Korff, Paloma Parvex, Laurent Cimasoni, et al.
Scientific Data
|
August 16, 2025
High-Density EEG Source Localisation of averaged interictal epileptic Discharges validated by surgical Outcome
Bernd J Vorderwülbecke, Margherita Carboni, Sebastien Tourbier, et al.
Cells
|
October 27, 2023
Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing <i>GNAO1</i> Mutation P170R
Yonika A Larasati, Gonzalo P Solis, Alexey Koval, et al.
Epilepsy Research
|
April 1, 2014
When is a child with status epilepticus likely to have Dravet syndrome?
François Le Gal, Sébastien Lebon, Gian Paolo Ramelli, et al.
Medcomm
|
May 8, 2025
Novel Mutation at Cys225 in <i>GNAO1</i>-Associated Developmental and Epileptic Encephalopathies: Clinical, Molecular, and Pharmacological Profiling of Case Studies
Yonika A Larasati, Gonzalo P Solis, Alexey Koval, et al.
American Journal of Medical Genetics. Part A
|
June 21, 2017
SERPINI1 pathogenic variants: An emerging cause of childhood-onset progressive myoclonic epilepsy
Emmanuelle Ranza, Stephanie Garcia-Tarodo, Konstantinos Varvagiannis, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 24, 2014
When should clinicians search for GLUT1 deficiency syndrome in childhood generalized epilepsies?
Sébastien Lebon, Philippe Suarez, Semsa Alija, et al.
Page
of 9