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2.
J Clin Neurophysiol ; 33(4): 312-6, 2016 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-27482795

RESUMO

This revision to the EEG Guidelines is an update incorporating current electroencephalography technology and practice and was previously published as Guideline 6. A discussion of methodology for the appropriate selection of reference electrodes is added. In addition, montages are added to assist with localization of abnormal activity in mesial frontal and anterior temporal regions.


Assuntos
Eletroencefalografia/normas , Neurofisiologia/normas , Guias de Prática Clínica como Assunto/normas , Sociedades Médicas/normas , Eletrodos/normas , Eletroencefalografia/instrumentação , Humanos , Estados Unidos
3.
Semin Pediatr Neurol ; 23(2): 180-6, 2016 05.
Artigo em Inglês | MEDLINE | ID: mdl-27544475

RESUMO

In this article, we review the treatment options for the pediatric epileptic encephalopathies and provide an update on the new and emerging therapies targeted at the underlying pathophysiology of many of these syndromes. We illustrate how the identification of the specific genetic and autoimmune causes has made possible the evaluation and development of novel, better targeted therapies, as and at times, avoidance of potentially offending agents.


Assuntos
Anticonvulsivantes/farmacologia , Epilepsias Mioclônicas/tratamento farmacológico , Síndrome de Landau-Kleffner/tratamento farmacológico , Síndrome de Lennox-Gastaut/tratamento farmacológico , Espasmos Infantis/tratamento farmacológico , Anticonvulsivantes/administração & dosagem , Epilepsias Mioclônicas/genética , Epilepsias Mioclônicas/imunologia , Humanos , Lactente , Síndrome de Landau-Kleffner/genética , Síndrome de Landau-Kleffner/imunologia , Síndrome de Lennox-Gastaut/genética , Síndrome de Lennox-Gastaut/imunologia , Espasmos Infantis/genética , Espasmos Infantis/imunologia
4.
Neurodiagn J ; 56(4): 253-260, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-28436788

RESUMO

This revision to the EEG Guidelines is an update incorporating current electroencephalography technology and practice and was previously published as Guideline 6. A discussion of methodology for the appropriate selection of reference electrodes is added. In addition, montages are added to assist with localization of abnormal activity in mesial frontal and anterior temporal regions.


Assuntos
Eletroencefalografia/normas , Eletroencefalografia/métodos , Humanos , Neurofisiologia , Sociedades Médicas , Estados Unidos
5.
Neurodiagn J ; 56(4): 245-252, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-28436791

RESUMO

This revision to the EEG Guidelines is an update incorporating current electroencephalography technology and practice and was previously published as Guideline 5. While the 10-10 system of electrode position nomenclature has been accepted internationally for almost two decades, it has not been used universally. The reasons for this and clinical scenarios when the 10-10 system provides additional localizing information are discussed in this revision. In addition, situations in which AF1/2, AF5/6, PO1/2 and PO5/6 electrode positions may be utilized for EEG recording are discussed.


Assuntos
Eletrodos , Eletroencefalografia/métodos , Padrões de Referência , Terminologia como Assunto , Humanos , Neurofisiologia , Sociedades Médicas , Estados Unidos
7.
Pediatr Clin North Am ; 62(3): 703-22, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-26022171

RESUMO

As the genetic etiologies of an expanding number of epilepsy syndromes are revealed, the complexity of the phenotype genotype correlation increases. As our review will show, multiple gene mutations cause different epilepsy syndromes, making identification of the specific mutation increasingly more important for prognostication and often more directed treatment. Examples of that include the need to avoid specific drugs in Dravet syndrome and the ongoing investigations of the potential use of new directed therapies such as retigabine in KCNQ2-related epilepsies, quinidine in KCNT1-related epilepsies, and memantine in GRIN2A-related epilepsies.


Assuntos
Epilepsia/genética , Mutação/genética , Adolescente , Idade de Início , Criança , Pré-Escolar , Epilepsia/diagnóstico , Epilepsia/terapia , Genótipo , Humanos , Lactente , Recém-Nascido , Fenótipo
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