Mitochondrial disorder related to the AFG3L2 gene in a boy with neurodevelopmental delay, ataxia and refractory epilepsy
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
Mitochondrial disorder related to the AFG3L2 gene in a boy with neurodevelopmental delay, ataxia and refractory epilepsy ; volume:81 ; number:S 01 ; year:2023 ; 01
Konferenz: SBN Conference 2022; 2022-11-09; Expo United Curitiba
Arquivos de neuro-psiquiatria ; 81, Heft S 01 (2023), 01
- Contributor
-
Vallim, Mariah Pereira de Andrade
Silva, Giulia Vilela
Rezende, Lorena Vilela
Junior, Rui Carlos Silva
- DOI
-
10.1055/s-0043-1774586
- URN
-
urn:nbn:de:101:1-2023110211302588217583
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 11:01 AM CEST
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Vallim, Mariah Pereira de Andrade
- Silva, Giulia Vilela
- Rezende, Lorena Vilela
- Junior, Rui Carlos Silva
Other Objects (12)
Management of Refractory Epilepsy
7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy
Personality traits in patients with refractory versus non-refractory epilepsy
Epilepsy in spinocerebellar ataxia type 8: a case report
Neuromodulation in refractory epilepsy: Brazilian specialists consensus
The use of cannabidiol in refractory epilepsy
Epilepsy surgery in pediatric refractory status epilepticus
A child with global neuroregression with refractory epilepsy
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
Double cortex syndrome – A rare cause of refractory epilepsy
Evaluation of nutritional status in children with refractory epilepsy
Management of Refractory Epilepsy
7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy
Personality traits in patients with refractory versus non-refractory epilepsy
Epilepsy in spinocerebellar ataxia type 8: a case report
Neuromodulation in refractory epilepsy: Brazilian specialists consensus
The use of cannabidiol in refractory epilepsy
Epilepsy surgery in pediatric refractory status epilepticus
A child with global neuroregression with refractory epilepsy
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
Double cortex syndrome – A rare cause of refractory epilepsy
Evaluation of nutritional status in children with refractory epilepsy
Management of Refractory Epilepsy
7p22.3 microdeletion: a case study of a patient with congenital heart defect, neurodevelopmental delay and epilepsy
Personality traits in patients with refractory versus non-refractory epilepsy
Epilepsy in spinocerebellar ataxia type 8: a case report
Neuromodulation in refractory epilepsy: Brazilian specialists consensus
The use of cannabidiol in refractory epilepsy
Epilepsy surgery in pediatric refractory status epilepticus
A child with global neuroregression with refractory epilepsy
Dissecting the genetic basis of comorbid epilepsy phenotypes in neurodevelopmental disorders
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy
Double cortex syndrome – A rare cause of refractory epilepsy