Oral valproic acid for epilepsy-long-term experience in therapy and side effects

T Gerstner, N Bell, S König - Expert opinion on pharmacotherapy, 2008 - Taylor & Francis
Valproic acid (VPA) is considered to be a drug of first choice and one of the most frequently-
prescribed antiepileptic drugs worldwide for the therapy of generalized and focal epilepsies …

The role of inflammatory mediators in epilepsy: focus on developmental and epileptic encephalopathies and therapeutic implications

A Orsini, T Foiadelli, G Costagliola, A Michev… - Epilepsy Research, 2021 - Elsevier
In recent years, there has been an increasing interest in the potential involvement of
neuroinflammation in the pathogenesis of epilepsy. Specifically, the role of innate immunity …

Randomized, single-blind, parallel clinical trial on efficacy of oral prednisolone versus intramuscular corticotropin on immediate and continued spasm control in west …

J Wanigasinghe, C Arambepola, SS Ranganathan… - Pediatric …, 2015 - Elsevier
Objective A single-center, single-blind, parallel-group, randomized clinical trial was
performed to test the null hypothesis that adrenocorticotropic hormone is not superior to high …

[HTML][HTML] Treatment and long term outcome in West syndrome: the clinical reality. A multicentre follow up study

L Lagae, H Verhelst, B Ceulemans, L De Meirleir… - Seizure, 2010 - Elsevier
We systematically reviewed the files of 51 infants presenting with infantile spasms and
hypsarrhythmia in order to study the initial treatment strategies and the long term outcome …

[HTML][HTML] Clinical spectrum and treatment outcome of West Syndrome in children from Northern India

JS Kaushik, B Patra, S Sharma, D Yadav, S Aneja - Seizure, 2013 - Elsevier
Purpose This study was intended to document the clinical profile and treatment outcome of
West syndrome in children attending a tertiary care center in Northern India. Method Data …

Metabolic etiologies in West syndrome

S Salar, SL Moshé, AS Galanopoulou - Epilepsia Open, 2018 - Wiley Online Library
West syndrome (WS) is an early life epileptic encephalopathy associated with infantile
spasms, interictal electroencephalography (EEG) abnormalities including high amplitude …

Treatment of infantile spasms: emerging insights from clinical and basic science perspectives

CE Stafstrom, BGW Arnason, TZ Baram… - Journal of child …, 2011 - journals.sagepub.com
Infantile spasms is an epileptic encephalopathy of early infancy with specific clinical and
electroencephalographic (EEG) features, limited treatment options, and a poor prognosis …

The EEG response to pyridoxine‐IV neither identifies nor excludes pyridoxine‐dependent epilepsy

LA Bok, NM Maurits, MA Willemsen, C Jakobs… - …, 2010 - Wiley Online Library
Purpose: Pyridoxine‐dependent epilepsy (PDE) is characterized by therapy‐resistant
seizures (TRS) responding to intravenous (IV) pyridoxine. PDE can be identified by …

Outcomes in treatment of infantile spasms with pulse methylprednisolone

JR Mytinger, M Quigg, WC Taft… - Journal of child …, 2010 - journals.sagepub.com
The authors report their experience with intravenous methylprednisolone for the treatment of
infantile spasms. A pulse dose of 20 mg/kg intravenous methylprednisolone on each of 3 …

Ketogenic diet therapy can improve ACTH-resistant West syndrome in Japan

Y Hirano, H Oguni, M Shiota, A Nishikawa… - Brain and …, 2015 - Elsevier
Purpose: Ketogenic diet therapy (KD) has been used to treat children with refractory
generalized epilepsy. We herein reported the efficacy of KD for West syndrome (WS) …