OBJECTIVE: Tuberous sclerosis complex (TSC) is a genetic disorder primarily characterized by the development of multisystem benign tumors. Epilepsy is the most common neurologic manifestation, affecting 80%-90% of TSC patients. The diffuse structural brain abnormalities and the multifocal nature of epilepsy in TSC pose diagnostic challenges when evaluating patients for epilepsy surgery. METHODS: We retrospectively reviewed the safety experience and efficacy outcomes of five adult TSC patients who were treated with direct brain-responsive neurostimulation (RNS System, NeuroPace, Inc). RESULTS: The average follow-up duration was 20 months. All five patients were responders (≥50% disabling seizure reduction) at last follow-up. The median reduc...
Epilepsy surgery is recommended in selected patients with Tuberous Sclerosis Complex (TSC). However,...
Tuberous sclerosis complex (TSC) is a rare genetic disorder caused by mutations in the TSC1 or TSC2 ...
Tuberous sclerosis is one of the genetically determined neurodermal syndromes, characterized by foca...
Background: Epilepsy is the most common neurological manifestation in individuals with tuberous scle...
Background: Although epilepsy affects most patients with tuberous sclerosis complex (TSC), little is...
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder affecting approxim...
TOSCA; Epilepsia; RegistroTOSCA; Epilèpsia; RegistreTOSCA; Epilepsy; RegistryBackground: Epilepsy is...
Objective. Tuberous sclerosis complex (TSC) is a m ultisystem genetic disorder associated with refra...
Tuberous sclerosis is a genetic disorder with incidence of 1 into 6000 birth. It is a multi-systemic...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
AbstractTuberous sclerosis complex (TSC) is a genetic disease in which overactivation of mechanistic...
Purpose: Tuberous sclerosis complex (TSC) is an autosomal-dominant genetic disorder and is a frequen...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
BACKGROUND: Surgery has become integral in treating children with tuberous sclerosis complex (TSC)-r...
Epilepsy surgery is recommended in selected patients with Tuberous Sclerosis Complex (TSC). However,...
Tuberous sclerosis complex (TSC) is a rare genetic disorder caused by mutations in the TSC1 or TSC2 ...
Tuberous sclerosis is one of the genetically determined neurodermal syndromes, characterized by foca...
Background: Epilepsy is the most common neurological manifestation in individuals with tuberous scle...
Background: Although epilepsy affects most patients with tuberous sclerosis complex (TSC), little is...
Tuberous sclerosis complex (TSC) is an autosomal dominant neurocutaneous disorder affecting approxim...
TOSCA; Epilepsia; RegistroTOSCA; Epilèpsia; RegistreTOSCA; Epilepsy; RegistryBackground: Epilepsy is...
Objective. Tuberous sclerosis complex (TSC) is a m ultisystem genetic disorder associated with refra...
Tuberous sclerosis is a genetic disorder with incidence of 1 into 6000 birth. It is a multi-systemic...
We report a case of tuberous sclerosis in a 19 years old teenage patient with generalized tonic-clon...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
AbstractTuberous sclerosis complex (TSC) is a genetic disease in which overactivation of mechanistic...
Purpose: Tuberous sclerosis complex (TSC) is an autosomal-dominant genetic disorder and is a frequen...
Objective: To present the baseline data of the international TuberOus SClerosis registry to increase...
BACKGROUND: Surgery has become integral in treating children with tuberous sclerosis complex (TSC)-r...
Epilepsy surgery is recommended in selected patients with Tuberous Sclerosis Complex (TSC). However,...
Tuberous sclerosis complex (TSC) is a rare genetic disorder caused by mutations in the TSC1 or TSC2 ...
Tuberous sclerosis is one of the genetically determined neurodermal syndromes, characterized by foca...