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H1N1 triggered recurrent acute necrotizing encephalopathy in a family with a T653I mutation in the RANBP2 gene.
Anand, Geetha; Visagan, Ravindran; Chandratre, Saleel; Segal, Shelley; Nemeth, Andrea H; Squier, Waney; Sheerin, Fintan; Neilson, Derek; Jayawant, Sandeep.
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  • Anand G; From the *Department of Paediatric Neurology; †Paediatric Infectious Disease and Immunology, John Radcliffe Hospital; ‡Department of Clinical Genetics, Churchill Hospital, Oxford University Hospitals NHS Trust; §Department of Clinical Neurosciences, University of Oxford; ¶Department of Neuropathology; ‖Department of Neuroradiology, John Radcliffe Hospital, Oxford University Hospitals NHS Trust, Oxfordshire, United Kingdom; and **Division of Human Genetics, Cincinnati Children's Hospital Medical
Pediatr Infect Dis J ; 34(3): 318-20, 2015 Mar.
Article en En | MEDLINE | ID: mdl-25170550
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Chaperonas Moleculares / Leucoencefalitis Hemorrágica Aguda / Sustitución de Aminoácidos / Proteínas de Complejo Poro Nuclear / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Mutación Idioma: En Revista: Pediatr Infect Dis J Asunto de la revista: DOENCAS TRANSMISSIVEIS / PEDIATRIA Año: 2015 Tipo del documento: Article
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Chaperonas Moleculares / Leucoencefalitis Hemorrágica Aguda / Sustitución de Aminoácidos / Proteínas de Complejo Poro Nuclear / Gripe Humana / Subtipo H1N1 del Virus de la Influenza A / Mutación Idioma: En Revista: Pediatr Infect Dis J Asunto de la revista: DOENCAS TRANSMISSIVEIS / PEDIATRIA Año: 2015 Tipo del documento: Article