Results 91 to 100 of about 1,141,201 (199)
Epilepsia Open, EarlyView.Abstract Objectives Adults with developmental and epileptic encephalopathies (DEEs) often enter adult neurology care without etiologic clarification because of incomplete transition from pediatric services, outdated investigations, and attenuation of childhood electro‐clinical features over time.
Giuseppe d’Orsi +10 more
wiley +1 more source
Vaccinations and Dravet Syndrome
, 2015 Investigators from various university hospitals, reference medical institutions and epilepsy centers, and the national institute for public health and environment in the Netherlands, studied the effect of vaccinations on seizure risk and disease course ...
Christian M. Korff, Korff, Christian
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Epilepsia Open, EarlyView.Abstract Objective Variants in the HCN1 gene cause a syndrome of childhood epilepsy and developmental disability with a broad phenotypic range. Many affected children manifest with early infantile epileptic encephalopathy (EIEE) and highly drug‐resistant epilepsy.
Marium N. Khan, Nicholas P. Poolos
wiley +1 more source
Antiseizure medication and Dravet syndrome
Dravet syndrome is a genetic disorder that causes a rare form of childhood epilepsy. It results from a mutation carried on the sodium ion channel gene.
MacVicar, Sonya
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Epilepsia Open, EarlyView.This graphical abstract provides an overview of the content from this post hoc analysis describing the trajectories of fenfluramine effectiveness and safety, along with dose changes over time, in patients with Lennox‐Gastaut syndrome. Abstract In the phase 3 randomized controlled trial (RCT; NCT03355209) of fenfluramine in Lennox–Gastaut syndrome (LGS),
Rima Nabbout +14 more
wiley +1 more source
Low-dose fenfluramine in the treatment of neurologic disorders: experience in Dravet syndrome
Therapeutic Advances in Neurological Disorders, 2015 In this paper, we review the experience with fenfluramine in epileptic and other paroxysmal disorders. Since the best available data are from the treatment of Dravet syndrome, we will focus primarily on this condition.
An-Sofie Schoonjans +2 more
doaj +1 more source
Lamotrigine can be beneficial in patients with Dravet syndrome.
, 2015 Dravet syndrome, a severe infantile epilepsy syndrome, is typically resistant to anti-epileptic drugs (AED). Lamotrigine (LTG), an AED that is effective for both focal and generalized seizures, has been reported to aggravate seizures in Dravet syndrome ...
Scheffer, I. +3 more
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Epilepsia Open, EarlyView.Abstract Objective Cannabidiol (CBD) has demonstrated promising effectiveness and tolerability as adjunctive treatment in patients with severe childhood epilepsies. This study investigated the effectiveness and tolerability of CBD in adults with a history of Dravet syndrome (DS), Lennox–Gastaut syndrome (LGS), or tuberous sclerosis complex (TSC ...
Sara Sánchez‐Gamino +7 more
wiley +1 more source
Fenfluramine: An Uncommon Cause of False Positive Urine Drug Testing: A Case Report
Annals of the Child Neurology SocietyBackground Fenfluramine is an antiseizure medication approved by the Food and Drug Administration for the treatment of Dravet syndrome in patients older than 2 years. Fenfluramine is an amphetamine derivative.
Maria Ghawji +2 more
doaj +1 more source
The family's experience of having a child with Dravet syndrome
, 2022 Cilj ovog istraživanja bio je dobiti uvid u iskustva obitelji djece s Dravet sindromom u Republici Hrvatskoj odnosno podatke o djetetu i njegovoj dijagnozi, informacije o kvaliteti i kvantiteti komunikacije roditelja sa stručnjacima, njihovo ...
Ćuruvija, Marta
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