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Clinical and Neuroimaging Features in Two Children with Mutations in the Mitochondrial ND5 Gene.
Sonam, Kothari; Bindu, P S; Taly, Arun B; Govindaraju, Chikkanna; Gayathri, Narayanappa; Arvinda, Hanumanthapura R; Nagappa, Madhu; Sinha, Sanjib; Khan, Nahid Akthar; Govindaraj, Periyasamy; Thangaraj, Kumarasamy.
Afiliación
  • Sonam K; Department of Clinical Neurosciences, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Bindu PS; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Taly AB; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Govindaraju C; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Gayathri N; Department of Neuropathology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Arvinda HR; Department of Neuroimaging and Interventional Radiology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Nagappa M; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Sinha S; Department of Neurology, National Institute of Mental Health and Neurosciences (NIMHANS), Bangalore, Karnataka, India.
  • Khan NA; Centre for Scientific and Industrial Research, Centre for Cellular and Molecular Biology (CSIR-CCMB), Hyderabad, Andhra Pradesh, India.
  • Govindaraj P; Centre for Scientific and Industrial Research, Centre for Cellular and Molecular Biology (CSIR-CCMB), Hyderabad, Andhra Pradesh, India.
  • Thangaraj K; Centre for Scientific and Industrial Research, Centre for Cellular and Molecular Biology (CSIR-CCMB), Hyderabad, Andhra Pradesh, India.
Neuropediatrics ; 46(4): 277-81, 2015 Aug.
Article en En | MEDLINE | ID: mdl-25974876
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encefalomiopatías Mitocondriales / Proteínas Mitocondriales / Complejo I de Transporte de Electrón Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Infant / Male Idioma: En Revista: Neuropediatrics Año: 2015 Tipo del documento: Article País de afiliación: India
Texto completo
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encefalomiopatías Mitocondriales / Proteínas Mitocondriales / Complejo I de Transporte de Electrón Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Child / Female / Humans / Infant / Male Idioma: En Revista: Neuropediatrics Año: 2015 Tipo del documento: Article País de afiliación: India