Search Results - "Serratosa, J."
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Randomized phase III study 306: Adjunctive perampanel for refractory partial-onset seizures
Published in Neurology (01-05-2012)“…To evaluate the efficacy and safety of perampanel 2, 4, and 8 mg/day added to 1-3 concomitant antiepileptic drugs (AEDs) in patients with uncontrolled…”
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Safety, efficacy and outcome-related factors of perampanel over 12 months in a real-world setting: The FYDATA study
Published in Epilepsy research (01-10-2016)“…Highlights • We report real-world data from 464 patients treated with perampanel over 1 year. • Efficacy and tolerability of perampanel were comparable with…”
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GLUT1 mutations are a rare cause of familial idiopathic generalized epilepsy
Published in Neurology (21-02-2012)“…The idiopathic generalized epilepsies (IGE) are the most common genetically determined epilepsies. However, the underlying genes are largely unknown. We…”
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Long-term safety and efficacy of eslicarbazepine acetate in patients with focal seizures: Results of the 1-year ESLIBASE retrospective study
Published in Epilepsy research (01-09-2014)“…Highlights • We evaluated eslicarbazepine acetate (ESL) in a clinical practice setting. • Three hundred and twenty-seven patients with poor seizure control or…”
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High-yield isolation of murine microglia by mild trypsinization
Published in Glia (01-12-2003)“…Microglia can be isolated with high purity but low yield by shaking off loosely adherent cells from mixed glial cultures. Here we describe a new technique for…”
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Lacosamide monotherapy in clinical practice: A retrospective chart review
Published in Acta neurologica Scandinavica (01-09-2018)“…Objective To assess effectiveness and tolerability of first‐line and conversion to lacosamide monotherapy for focal seizures. Materials and Methods…”
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Safety and tolerability of perampanel: a review of clinical trial data
Published in Acta neurologica Scandinavica (01-04-2013)“…The Phase II and Phase III clinical development program of perampanel is providing a wealth of data on the safety and tolerability of this…”
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Lafora disease due to EPM2B mutations : A clinical and genetic study
Published in Neurology (22-03-2005)“…To study EPM2B gene mutations and genotype-phenotype correlations in patients with Lafora disease. The authors performed a clinical and mutational analysis of…”
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PCAF regulates the stability of the transcriptional regulator and cyclin-dependent kinase inhibitor p27Kip1
Published in Nucleic acids research (01-08-2012)“…P27(Kip1) (p27) is a member of the Cip/Kip family of cyclin-dependent kinase inhibitors. Recently, a new function of p27 as transcriptional regulator has been…”
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EFFICACY AND SAFETY OF ESLICARBAZEPINE-ACETATE IN ELDERLY PATIENTS WITH FOCAL EPILEPSY: CASE SERIES
Published in Seizure (London, England) (01-05-2017)“…Abstract Purpose Eslicarbazepine-acetate (ESL) is a third generation antiepileptic drug licensed as adjunctive therapy in adults with focal seizures. Efficacy…”
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Socio-occupational and employment profile of patients with epilepsy
Published in Epilepsy & behavior (01-07-2011)“…Abstract Objective Epilepsy has a significant impact on quality of life. Many studies have observed higher unemployment rates among patients with epilepsy…”
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Stress response of extensively reared young bulls being transported to growing-finishing farms under Spanish summer commercial conditions
Published in Livestock science (01-12-2008)“…To evaluate the effect of Spanish summer commercial journeys on the stress response of young bulls born and reared under extensive conditions, 2 replicates of…”
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Novel mutation in STXBP1 gene in a patient with non-lesional Ohtahara syndrome
Published in Neurologia (Barcelona, Spain) (01-10-2016)“…Ohtahara syndrome (OS, OMIM#308350, ORPHA1934) is an early-onset epileptic encephalopathy (EOEE) characterised by spasms, intractable seizures,…”
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Variant Intestinal-Cell Kinase in Juvenile Myoclonic Epilepsy
Published in The New England journal of medicine (15-03-2018)“…In this study, variants in the gene encoding intestinal-cell kinase ( ICK ) were associated with 7% of cases of juvenile myoclonic epilepsy among 310 patients…”
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A Novel Protein Tyrosine Phosphatase Gene Is Mutated in Progressive Myoclonus Epilepsy of the Lafora Type (EPM2)
Published in Human molecular genetics (01-02-1999)“…Progressive myoclonus epilepsy of the Lafora type or Lafora disease (EPM2; McKusick no. 254780) is an autosomal recessive disorder characterized by epilepsy,…”
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V28. KCNA2 mutations cause epileptic encephalopathy by gain- or loss-of channel function
Published in Clinical neurophysiology (01-08-2015)“…Epileptic encephalopathies (EE) are a heterogeneous group of epilepsy syndromes associated with severe cognitive and behavioral disturbances. Amongst others,…”
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Strategies to detect adverse effects of antiepileptic drugs in clinical practice
Published in Epilepsy & behavior (01-07-2008)“…Abstract Objective The aim was to study the frequency and types of adverse effects (AEs) in patients treated with antiepileptic drugs (AEDs) according to the…”
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Hepatic disease as the first manifestation of progressive myoclonus epilepsy of lafora
Published in Neurology (24-04-2007)“…Lafora disease (LD; progressive myoclonus epilepsy type 2; EPM2) is an autosomal recessive disorder caused by mutations in the EPM2A and EPM2B genes. LD is…”
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Effect of lamotrigine on sexual function in patients with epilepsy
Published in Seizure (London, England) (01-04-2006)“…To assess the course of sexual function in epilepsy patients treated with lamotrigine. This open study included 141 patients treated with lamotrigine for a…”
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