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PedAM

Pediatric Disease Annotations & Medicines




Disease epilepsy
Phenotype C0041341|tuberous sclerosis
Sentences 32
PubMedID- 20041940 The natural history of epilepsy in tuberous sclerosis complex.
PubMedID- 25591831 Conclusion: various preclinical models provide substantial evidence for the role of mtor inhibition in the treatment of epilepsy in individuals with tuberous sclerosis complex.
PubMedID- 19369101 epilepsy associated with tuberous sclerosis complex (tsc) is characterized by early onset and intractable seizures in the majority of children.
PubMedID- 23219029 Clobazam therapy of refractory epilepsy in tuberous sclerosis complex.
PubMedID- 23861807 They also found associations between autistic traits and epilepsy in patients with tuberous sclerosis.
PubMedID- 22019663 Multimodal approach in the surgical treatment of refractory epilepsy associated with tuberous sclerosis complex: a series of three cases.
PubMedID- 21481739 Cortical tubers, cognition, and epilepsy in tuberous sclerosis.
PubMedID- 26067126 Treatment of epilepsy associated with tuberous sclerosis remains a major challenge, with more than 60% of patients having ongoing seizures.
PubMedID- 21959128 Purpose: to elucidate the functional characteristics of cortical tubers that might be responsible for epilepsy in tuberous sclerosis complex (tsc), proton magnetic resonance spectroscopy ((1)h-mrs) and [123i] iomazenil (123i-imz) single photon emission computed tomography (spect) were performed.
PubMedID- 24379984 Clinical trials are ongoing to further examine the effects of everolimus on epilepsy associated with tuberous sclerosis complex.
PubMedID- 24044547 epilepsy associated with tuberous sclerosis generally begins during the first year of life and, in most patients, in the first few months.
PubMedID- 26060906 epilepsy in tuberous sclerosis: phenotypes, mechanisms, and treatments.
PubMedID- 22247914 Clinical progress of epilepsy in children with tuberous sclerosis: prognostic factors for seizure outcome.
PubMedID- 23883617 Abnormal inhibitory circuits in cortical tubers of tuberous sclerosis, associated with refractory epilepsy, are accompanied by aberrant expression of parvalbumin and calbindin d28k in the dysplastic cortex [226].
PubMedID- 24698169 Background/purpose: to clarify the relationship between neuroimaging findings, neuropsychiatric comorbidities, and epilepsy in patients with tuberous sclerosis complex (tsc) in taiwan.
PubMedID- 25030328 epilepsy in newborns with tuberous sclerosis complex.
PubMedID- 23798472 Everolimus treatment of refractory epilepsy in tuberous sclerosis complex.
PubMedID- 20636971 Can we change the course of epilepsy in tuberous sclerosis complex.
PubMedID- 26539097 Other studies reported results from homogeneous patient groups with various locations of the epileptogenic zone, e.g., epilepsy in tuberous sclerosis (okanishi et al., 2014) and neocortical epilepsy (cho et al., 2014).
PubMedID- 23743820 Rapamycin has a beneficial effect on controlling epilepsy in children with tuberous sclerosis complex: results of 7 children from a cohort of 86.
PubMedID- 22695035 Management of epilepsy associated with tuberous sclerosis complex (tsc): clinical recommendations.
PubMedID- 25360852 Object: tuberous sclerosis complex (tsc) with medically refractory epilepsy is characterized by multifocal brain abnormalities, traditionally indicating poor surgical candidacy.
PubMedID- 22142783 Long-term neurological outcome in children with early-onset epilepsy associated with tuberous sclerosis.
PubMedID- 20682200 Vagus nerve stimulation for refractory epilepsy in tuberous sclerosis.
PubMedID- 22983234 Treatment of epilepsy in tuberous sclerosis is similar to epilepsy resulting from other cases and includes anticonvulsant medications, the epilepsy surgery, the vagus nerve stimulation and the ketogenic diet.
PubMedID- 26046563 epilepsy in children with tuberous sclerosis complex: chance of remission and response to antiepileptic drugs.
PubMedID- 24304436 Purpose: prevalence and long-term outcome of epilepsy in tuberous sclerosis complex (tsc) is reported to be variable, and the reasons for this variability are still controversial.
PubMedID- 23703058 Conclusions: epilepsy in tuberous sclerosis is relatively benign and an acceptable degree of control is achieved in most cases with a number of the antiepileptic drugs recommended in the treatment guidelines.
PubMedID- 25847341 Its role in the treatment of epilepsy in individuals with tuberous sclerosis complex (tsc) has yet to be determined.
PubMedID- 24556736 Target-oriented treatments such as rapamycin and everolimus are currently under clinical investigation to prevent epilepsy in patients with tuberous sclerosis.
PubMedID- 22000822 Effective everolimus treatment of inoperable, life-threatening subependymal giant cell astrocytoma and intractable epilepsy in a patient with tuberous sclerosis complex.
PubMedID- 23250840 epilepsy in tuberous sclerosis complex.

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