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EEG abnormalities in patients with chronic neuronopathic Gaucher disease: A retrospective review.
Poffenberger, Chelsie N; Inati, Sara; Tayebi, Nahid; Stubblefield, Barbara K; Ryan, Emory; Schiffmann, Raphael; Sidransky, Ellen; Lopez, Grisel.
Afiliación
  • Poffenberger CN; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
  • Inati S; Electroencephalography (EEG) Section, Office of the Clinical Director, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD, United States of America.
  • Tayebi N; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
  • Stubblefield BK; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
  • Ryan E; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
  • Schiffmann R; Baylor Scott & White Research Institute, Dallas, TX, United States of America.
  • Sidransky E; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America. Electronic address: sidranse@mail.nih.gov.
  • Lopez G; Section on Molecular Neurogenetics, Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, United States of America.
Mol Genet Metab ; 131(3): 358-363, 2020 11.
Article en En | MEDLINE | ID: mdl-33183916
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Convulsiones / Epilepsias Mioclónicas / Enfermedad de Gaucher / Malformaciones del Sistema Nervioso Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article
Texto completo
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Convulsiones / Epilepsias Mioclónicas / Enfermedad de Gaucher / Malformaciones del Sistema Nervioso Tipo de estudio: Prognostic_studies / Risk_factors_studies Idioma: En Revista: Mol Genet Metab Asunto de la revista: BIOLOGIA MOLECULAR / BIOQUIMICA / METABOLISMO Año: 2020 Tipo del documento: Article