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Benign hereditary chorea: phenotype, prognosis, therapeutic outcome and long term follow-up in a large series with new mutations in the TITF1/NKX2-1 gene.
Gras, Domitille; Jonard, Laurence; Roze, Emmanuel; Chantot-Bastaraud, Sandra; Koht, Jeanette; Motte, Jacques; Rodriguez, Diana; Louha, Malek; Caubel, Isabelle; Kemlin, Isabelle; Lion-François, Laurence; Goizet, Cyril; Guillot, Loic; Moutard, Marie-Laure; Epaud, Ralph; Héron, Bénédicte; Charles, Perrine; Tallot, Marilyn; Camuzat, Agnès; Durr, Alexandra; Polak, Michel; Devos, David; Sanlaville, Damien; Vuillaume, Isabelle; Billette de Villemeur, Thierry; Vidailhet, Marie; Doummar, Diane.
Affiliation
  • Gras D; AP-HP, Service de Neuropédiatrie, Hôpital Trousseau, Paris, France.
J Neurol Neurosurg Psychiatry ; 83(10): 956-62, 2012 Oct.
Article in En | MEDLINE | ID: mdl-22832740
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tetrabenazine / Transcription Factors / Nuclear Proteins / Chorea / Adrenergic Uptake Inhibitors / Chromosome Disorders / Mutation Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Country/Region as subject: Europa Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2012 Document type: Article Affiliation country: France
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tetrabenazine / Transcription Factors / Nuclear Proteins / Chorea / Adrenergic Uptake Inhibitors / Chromosome Disorders / Mutation Type of study: Clinical_trials / Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Country/Region as subject: Europa Language: En Journal: J Neurol Neurosurg Psychiatry Year: 2012 Document type: Article Affiliation country: France