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Journal of Child Neurology
|
April 9, 2013
Language regression associated with autistic regression and electroencephalographic (EEG) abnormalities: a prospective study
Anna Maria Chilosi, Paola Brovedani, Anna Rita Ferrari, et al.
Epilepsy Research
|
August 12, 2011
Intrinsic epileptogenicity of gangliogliomas may be independent from co-occurring focal cortical dysplasia
Carmen Barba, Roland Coras, Flavio Giordano, et al.
Seizure
|
June 18, 2005
Topiramate monotherapy as broad-spectrum antiepileptic drug in a naturalistic clinical setting
Renzo Guerrini, Johannes Carpay, Joze Groselj, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 24, 2008
The potential action of galactose as a "chemical chaperone": increase of beta galactosidase activity in fibroblasts from an adult GM1-gangliosidosis patient
Anna Caciotti, Maria Alice Donati, Alessandra d'Azzo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
September 29, 2021
Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome
Roberta Solazzi, Elena Fiorini, Elena Parrini, et al.
Epilepsy & Behavior : E&B
|
November 20, 2012
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature
Giulia Valvo, Francesca Novara, Paola Brovedani, et al.
Epilepsia
|
February 23, 2012
Impaired object identification in idiopathic childhood occipital epilepsy
Claudia Brancati, Carmen Barba, Tiziana Metitieri, et al.
Journal of Medical Genetics
|
July 31, 2024
Double gonosomal mosaicism as an unusual hereditary mechanism in familial <i>GRIN2A</i>-related disorder
Valentina Cetica, Mara Cavallin, Maria Luisa Ricci, et al.
Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Parkinsonism & Related Disorders
|
October 18, 2019
A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3
Mario Mastrangelo, Davide Mei, Serena Cesario, et al.
Page
of 61
Search research articles
Search
Showing results (151-160 of 610) with videos related to
Sort By:
Page
of 61
Journal of Child Neurology
|
April 9, 2013
Language regression associated with autistic regression and electroencephalographic (EEG) abnormalities: a prospective study
Anna Maria Chilosi, Paola Brovedani, Anna Rita Ferrari, et al.
Epilepsy Research
|
August 12, 2011
Intrinsic epileptogenicity of gangliogliomas may be independent from co-occurring focal cortical dysplasia
Carmen Barba, Roland Coras, Flavio Giordano, et al.
Seizure
|
June 18, 2005
Topiramate monotherapy as broad-spectrum antiepileptic drug in a naturalistic clinical setting
Renzo Guerrini, Johannes Carpay, Joze Groselj, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
June 24, 2008
The potential action of galactose as a "chemical chaperone": increase of beta galactosidase activity in fibroblasts from an adult GM1-gangliosidosis patient
Anna Caciotti, Maria Alice Donati, Alessandra d'Azzo, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
September 29, 2021
Early-onset bradykinetic rigid syndrome and reflex seizures in a child with PURA syndrome
Roberta Solazzi, Elena Fiorini, Elena Parrini, et al.
Epilepsy & Behavior : E&B
|
November 20, 2012
22q11.2 Microduplication syndrome and epilepsy with continuous spikes and waves during sleep (CSWS). A case report and review of the literature
Giulia Valvo, Francesca Novara, Paola Brovedani, et al.
Epilepsia
|
February 23, 2012
Impaired object identification in idiopathic childhood occipital epilepsy
Claudia Brancati, Carmen Barba, Tiziana Metitieri, et al.
Journal of Medical Genetics
|
July 31, 2024
Double gonosomal mosaicism as an unusual hereditary mechanism in familial <i>GRIN2A</i>-related disorder
Valentina Cetica, Mara Cavallin, Maria Luisa Ricci, et al.
Epilepsia
|
April 6, 2011
The genetics of Dravet syndrome
Carla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
Parkinsonism & Related Disorders
|
October 18, 2019
A novel developmental encephalopathy with epilepsy and hyperkinetic movement disorders associated with a deletion of the sodium channel gene cluster on chromosome 2q24.3
Mario Mastrangelo, Davide Mei, Serena Cesario, et al.
Page
of 61