Myoclonus in childhood-onset neurogenetic disorders: The importance of early identification and treatment.

van Egmond, Martje E; Elting, Jan Willem J; Kuiper, Anouk; Zutt, Rodi; Heineman, Kirsten R; Brouwer, Oebele F; Sival, Deborah A; Willemsen, Michel A; Tijssen, Marina A J; de Koning, Tom J

van Egmond, Martje E; Elting, Jan Willem J; Kuiper, Anouk; Zutt, Rodi; Heineman, Kirsten R; Brouwer, Oebele F; Sival, Deborah A; Willemsen, Michel A; Tijssen, Marina A J; de Koning, Tom J.

Afiliação

van Egmond ME; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands. Electronic address: m.e.van.egmond@umcg.nl.
Elting JW; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
Kuiper A; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
Zutt R; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
Heineman KR; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
Brouwer OF; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
Sival DA; University of Groningen, University Medical Center Groningen, Department of Pediatrics, Groningen, The Netherlands.
Willemsen MA; Radboud University Medical Center, Department of Pediatric Neurology, Nijmegen, The Netherlands.
Tijssen MA; University of Groningen, University Medical Center Groningen, Department of Neurology, Groningen, The Netherlands.
de Koning TJ; University of Groningen, University Medical Center Groningen, Department of Pediatrics, Groningen, The Netherlands; University of Groningen, University Medical Center Groningen, Department of Genetics, Groningen, The Netherlands.

Eur J Paediatr Neurol ; 19(6): 726-9, 2015 Nov.

Article em En | MEDLINE | ID: mdl-26232052

Assuntos

Mioclonia/etiologia; Doenças do Sistema Nervoso/complicações; Doenças do Sistema Nervoso/genética; Anticonvulsivantes/uso terapêutico; Ataxia Telangiectasia/etiologia; Ataxia Telangiectasia/genética; Encefalopatias/complicações; Encefalopatias/genética; Criança; Síndrome de Coffin-Lowry/etiologia; Síndrome de Coffin-Lowry/genética; Diagnóstico Precoce; Eletromiografia; Epilepsias Mioclônicas/genética; Epilepsia/etiologia; Epilepsia/genética; Feminino; Humanos; Masculino; Transtornos dos Movimentos/etiologia; Transtornos dos Movimentos/genética; Mioclonia/tratamento farmacológico; Canal de Sódio Disparado por Voltagem NAV1.1/genética; Doenças do Sistema Nervoso/tratamento farmacológico; Adulto Jovem

Palavras-chave

Movement disorders; Myoclonus; Neurogenetic disorders

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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Mioclonia / Doenças do Sistema Nervoso Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Screening_studies Limite: Adult / Child / Female / Humans / Male Idioma: En Revista: Eur J Paediatr Neurol Assunto da revista: NEUROLOGIA / PEDIATRIA Ano de publicação: 2015 Tipo de documento: Article

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