Epilepsy Absence
Mostrando 1-12 de 54 artigos, teses e dissertações.
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1. Use of cannabidiol in the treatment of epilepsy: Lennox-Gastaut syndrome, Dravet syndrome, and tuberous sclerosis complex
SUMMARY OBJECTIVE: The objective of this systematic review with meta-analysis was to evaluate the efficacy, safety, and short- and long-term tolerability of cannabidiol (CBD), as an adjunct treatment, in children and adults with Dravet syndrome (SD), Lennox-Gataut syndrome (LGS), or tuberous sclerosis complex (TSC), with inadequate control of seizures. MET
Revista da Associação Médica Brasileira. Publicado em: 2022
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2. Micronutrients: Speculation on Inborn Errors, Nutrigenomics, Evolution, the Microbiome, and Nutritional Immunity
Abstract Many micronutrients or cofactors derived from micronutrients are highly reactive, hence their role in catalysis of reactions by enzymes. The concentration of cofactors has to be kept low to avoid unwanted reactions while allowing them to bind to the (apo)enzymes that need them. A new disorder causing B6-responsive epilepsy (proline synthetase cotran
J. inborn errors metab. screen.. Publicado em: 28/02/2019
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3. Transcranial direct current stimulation and repetitive transcranial magnetic stimulation in consultation-liaison psychiatry
Patients with clinical diseases often present psychiatric conditions whose pharmacological treatment is hampered due to hazardous interactions with the clinical treatment and/or disease. This is particularly relevant for major depressive disorder, the most common psychiatric disorder in the general hospital. In this context, nonpharmacological interventions
Braz J Med Biol Res. Publicado em: 02/10/2013
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4. Análise dos genes GHRH e GL12 em pacientes com deficiência de hormônio do crescimento congênita / GHRH and GLI2 genes analysis in patients with congenital growth hormone deficiency
Introduction: Alterations in genes related to GH secretion and pituitary organogenesis have been identified in patients with congenital GH deficiency (GHD). However, in only few cases of GHD the etiology has been established. GH-releasing hormone (GHRH) is an obvious candidate to explain isolated GH deficiency (IGHD). Previous reports in the literature did n
IBICT - Instituto Brasileiro de Informação em Ciência e Tecnologia. Publicado em: 14/02/2012
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5. A caracterização do perfil de expressão gênica em larga escala em modelos genéticos de epilepsia fornece elementos para entender os mecanismos envolvidos na epileptogênese em roedores
OBJETIVO: O objetivo desse trabalho foi caracterizar e comparar o perfil genético de dois modelos de epilepsia em roedores (Wistar Audiogenic Rat - WAR e generalized epilepsy with absence seizures - GEAS) através da análise da expressão gênica em larga escala. MÉTODOS: Para a análise do perfil de expressão gênica foi utilizada a técnica de microarr
J. epilepsy clin. neurophysiol.. Publicado em: 2012
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6. Estudo crítico dos modelos experimentais em epilepsia espontânea do tipo ausência / Critical study of experimental models of absence-like epilepsy
A epilepsia é uma das afecções neurológica mais comum na população mundial. Trata-se de uma condição crônica altamente incapacitante que acomete indivíduos de ambos os sexos e de todas as faixas etárias, com um discreto predomínio em homens e, maior freqüência em crianças abaixo de dois anos e idosos acima de 65 anos. As conseqüências de mor
Publicado em: 2011
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7. Electrophysiological study in vitro of the hippocampus and of the susceptibility against two experimental models of epilepsy in the rodent Trinomys yonenagae. / Estudo eletrofisiológico in vitro do hipocampo e da suscetibilidade frente a dois modelos experimentais de epilepsia no roedor Trinomys yonenagae.
Trinomys yonenagae (TY) is a fossorial rodent dweller of sand dunes of the Caatinga, pertaining to Echimydae family and known locally as rabo de facho. The observation of some animals of this species show spontaneous seizures stimulated us the study of some characteristics of its nervous system that could to be subjacents to this condition. Through technique
Publicado em: 2009
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8. Estudo clÃnico e eletrocefalogrÃfico de crises de ausÃncias tÃpicas: sÃrie de 63 casos / Clinical and electroencephalographic study of typical absences seizures: series of 63 cases
Foram estudadas atravÃs de vÃdeo-EEG 957 crises de ausÃncias tÃpicas em 63 pacientes com idades de dois anos a 64 anos. AusÃncias tÃpicas foram definidas conforme a ClassificaÃÃo da Liga Internacional contra a Epilepsia (ILAE, 1981): "crise de inÃcio abrupto, com interrupÃÃo das atividades, perda do contato e possÃvel rotaÃÃo dos olhos para cim
Publicado em: 2008
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9. The trajectory of Laila in the AMA : intertwined stories / A trajetoria de Laila no AMA : historias entrelaçadas
This research sought to understand which elements are important for working with people with disabilities. The problem that gave rise to this research was the absence of longitudinal studies with children with disabilities engaged in extra-curricular adapted motor activity programs. Therefore, it was decided to carry out a case study, with a qualitative, lon
Publicado em: 2008
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10. Expressão e purificação de proteinas relacionadas a epilepsia / Expression and purification of epilepsy related proteins
Non-ion channel genes, as LGI1 and EFHC1, have been shown to indirectly affect ion channel currents in genetically determined epilepsy syndromes. LGI1 (Leucine-rich, glioma inactivated gene 1) is linked to a rare form of partial epilepsy (autosomal dominant partial epilepsy with auditory features, ADPEAF). Recently, LGI1 protein was associated with ADAM22 in
Publicado em: 2007
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11. Avaliação eletrofisiológica in vitro de drogas antiepilépticas em fatias hipocampais humanas provenientes de pacientes portadores de epilepsia do lobo temporal refratária ao tratamento medicamentoso
The absence of a satisfactory response to antiepileptic drug (AED) therapy, is an unresolved problem in a significant number of epileptic patients. Mechanisms of intractability are not well understood but may include a combination of poor penetration of AED across a functionally altered blood-brain barrier owing to increased expression of multiple drug resis
Journal of Epilepsy and Clinical Neurophysiology. Publicado em: 2006-06
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12. Absence-like seizures in adult rats following pilocarpine-induced status epilepticus early in life
Administration of pilocarpine causes epilepsy in rats if status epilepticus (SE) is induced at an early age. To determine in detail the electrophysiological patterns of the epileptogenic activity in these animals, 46 Wistar rats, 7-17 days old, were subjected to SE induced by pilocarpine and electro-oscillograms from the cortex, hippocampus, amygdala, thalam
Brazilian Journal of Medical and Biological Research. Publicado em: 2003-12