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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 14, 2011
Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype
Yunus Kasim Terzi, Burcu Sirin, Guzen Hosgor, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
October 7, 2025
Correction to: Lower risk of seizure recurrence with levetiracetam and oxcarbazepine after withdrawal in pediatric epilepsy: a pilot study
Dilek Cebeci, Ebru Arhan, Ercan Demir, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 20, 2025
Lower risk of seizure recurrence with levetiracetam and oxcarbazepine after withdrawal in pediatric epilepsy: a pilot study
Dilek Cebeci, Ebru Arhan, Ercan Demir, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 2011
Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype
Yunus Kasim Terzi, Burcu Sirin, Esra Serdaroglu, et al.
Neurology
|
July 25, 2023
Access to Pediatric Neurology Training and Services Worldwide: A Survey by the International Child Neurology Association
Jo M Wilmshurst, Coriene Catsman-Berrevoets, Donald L Gilbert, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay
Ayşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 22, 2024
Report from the child neurology education and training workshop at the International Child Neurology Congress 2024: Expert'saddressing the training gap
Jo M Wilmshurst, Dara Vf Albert, Asif Doja, et al.
Frontiers in Neurology
|
June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategies
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 12, 2026
Transition from paediatric to adult care in paediatric-onset neurological disorders in Europe: A survey and scoping review
Dana Craiu, Maria T Papadopoulou, Jasna Orazem Mrak, et al.
Epilepsy & Behavior : E&B
|
March 24, 2026
The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort study
Pinar Ozkan Kart, Esra Serdaroglu, Nihal Yildiz, et al.
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Search research articles
Search
Showing results (11-20 of 21) with videos related to
Sort By:
Page
of 3
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 14, 2011
Two pathogenic NF1 gene mutations identified in DNA from a child with mild phenotype
Yunus Kasim Terzi, Burcu Sirin, Guzen Hosgor, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
October 7, 2025
Correction to: Lower risk of seizure recurrence with levetiracetam and oxcarbazepine after withdrawal in pediatric epilepsy: a pilot study
Dilek Cebeci, Ebru Arhan, Ercan Demir, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
|
September 20, 2025
Lower risk of seizure recurrence with levetiracetam and oxcarbazepine after withdrawal in pediatric epilepsy: a pilot study
Dilek Cebeci, Ebru Arhan, Ercan Demir, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
July 7, 2011
Absence of exon 17 c.2970-2872delAAT mutation in Turkish NF1 patients with mild phenotype
Yunus Kasim Terzi, Burcu Sirin, Esra Serdaroglu, et al.
Neurology
|
July 25, 2023
Access to Pediatric Neurology Training and Services Worldwide: A Survey by the International Child Neurology Association
Jo M Wilmshurst, Coriene Catsman-Berrevoets, Donald L Gilbert, et al.
Cold Spring Harbor Molecular Case Studies
|
May 6, 2016
A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay
Ayşegül Ozantürk, Erica E Davis, Aniko Sabo, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 22, 2024
Report from the child neurology education and training workshop at the International Child Neurology Congress 2024: Expert'saddressing the training gap
Jo M Wilmshurst, Dara Vf Albert, Asif Doja, et al.
Frontiers in Neurology
|
June 21, 2024
Dyskinetic crisis in <i>GNAO1</i>-related disorders: clinical perspectives and management strategies
Jana Domínguez Carral, Carola Reinhard, Darius Ebrahimi-Fakhari, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 12, 2026
Transition from paediatric to adult care in paediatric-onset neurological disorders in Europe: A survey and scoping review
Dana Craiu, Maria T Papadopoulou, Jasna Orazem Mrak, et al.
Epilepsy & Behavior : E&B
|
March 24, 2026
The efficacy and tolerability of lacosamide adjunctive therapy in children with drug-refractory epilepsy: A nationwide Turkish cohort study
Pinar Ozkan Kart, Esra Serdaroglu, Nihal Yildiz, et al.
Page
of 3