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The clinical and genetic heterogeneity of paroxysmal dyskinesias.
Gardiner, Alice R; Jaffer, Fatima; Dale, Russell C; Labrum, Robyn; Erro, Roberto; Meyer, Esther; Xiromerisiou, Georgia; Stamelou, Maria; Walker, Matthew; Kullmann, Dimitri; Warner, Tom; Jarman, Paul; Hanna, Mike; Kurian, Manju A; Bhatia, Kailash P; Houlden, Henry.
Afiliación
  • Gardiner AR; 1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Jaffer F; 1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Dale RC; 3 Paediatrics and Child Health, Children's Hospital, Westmead, University of Sydney, Australia.
  • Labrum R; 4 Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Erro R; 5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Meyer E; 6 Developmental Neurosciences, UCL Institute of Child Health, London WC1N 3JH, UK.
  • Xiromerisiou G; 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 7 Department of Neurology, Papageorgiou Hospital, Thessaloniki University of Athens, Greece.
  • Stamelou M; 5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 8 Department of Neurology University of Athens, Greece 9 Department of Neurology, Philipps University, Marburg, Germany.
  • Walker M; 10 Department of Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Kullmann D; 10 Department of Experimental Epilepsy, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Warner T; 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Jarman P; 5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Hanna M; 1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Kurian MA; 6 Developmental Neurosciences, UCL Institute of Child Health, London WC1N 3JH, UK 11 Department of Neurology, Great Ormond Street Hospital, London WC1N, UK.
  • Bhatia KP; 5 Department of Motor Neuroscience and Movement Disorders, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Houlden H; 1 MRC Centre for Neuromuscular Diseases, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 2 Department of Molecular Neuroscience, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK 4 Neurogenetics Laboratory, UCL Institute of Neurology, Queen Square, London WC1N 3BG, UK h.hou
Brain ; 138(Pt 12): 3567-80, 2015 Dec.
Article en En | MEDLINE | ID: mdl-26598494
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Corea / Heterogeneidad Genética / Transportador de Glucosa de Tipo 1 / Proteínas de la Membrana / Proteínas Musculares / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido
Texto completo
Imprimir
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PubMed Links
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Corea / Heterogeneidad Genética / Transportador de Glucosa de Tipo 1 / Proteínas de la Membrana / Proteínas Musculares / Proteínas del Tejido Nervioso Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Año: 2015 Tipo del documento: Article País de afiliación: Reino Unido