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Movement Disorders (revue) - Checkpoint (Istex)

Index « Keywords » - entrée « primary torsion dystonia »
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primary tic disorders < primary torsion dystonia < primary writing tremor  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 8.
Ident.Authors (with country if any)Title
000D99 (2009) Monica Bonetti [Italie] ; Chiara Barzaghi [Italie] ; Francesco Brancati [Italie] ; Alessandro Ferraris [Italie] ; Emanuele Bellacchio [Italie] ; Alessandro Giovanetti [Italie] ; Tamara Ialongo [Italie] ; Giovanna Zorzi [Italie] ; Carla Piano [Italie] ; Martina Petracca [Italie] ; Alberto Albanese [Italie] ; Nardo Nardocci [Italie] ; Bruno Dallapiccola [Italie] ; Anna Rita Bentivoglio [Italie] ; Barbara Garavaglia [Italie] ; Enza Maria Valente [Italie]Mutation screening of the DYT6/THAP1 gene in Italy
002036 (2006) Mattia Gambarin [Italie] ; Enza Maria Valente [Italie] ; Paolo Liberini [Italie] ; Giuseppe Barrano [Italie] ; Alberto Bonizzato [Italie] ; Alessandro Padovani [Italie] ; Giuseppe Moretto [Italie] ; Mirta Fiorio [Italie] ; Bruno Dallapiccola [Italie] ; Nicola Smania [Italie] ; Antonio Fiaschi [Italie] ; Michele Tinazzi [Italie]Atypical phenotypes and clinical variability in a large Italian family with DYT1–primary torsion dystonia
002597 (2004) Anna Rita Bentivoglio [Italie] ; Tamara Ialongo [Italie] ; M. Fiorella Contarino [Italie] ; Enza M. Valente [Italie] ; Alberto Albanese [Italie]Phenotypic characterization of DYT13 primary torsion dystonia
002654 (2004) Kathrin Grundmann [Allemagne] ; Ulrike Laubis-Herrmann [Allemagne] ; Dirk Dressler [Allemagne] ; Juliane Vollmer-Haase [Allemagne] ; Peter Bauer [Allemagne] ; Manfred Stuhrmann [Allemagne] ; Thorsten Schulte [Allemagne] ; Ludger Schöls [Allemagne] ; Helge Topka [Allemagne] ; Olaf Riess [Allemagne]Lack of mutations in the epsilon‐sarcoglycan gene in patients with different subtypes of primary dystonias
002856 (2003) Thomas Gasser [Allemagne] ; Susan Bressman [États-Unis] ; Alexandra Dürr [France] ; Joseph Higgins [États-Unis] ; Thomas Klockgether [Allemagne] ; Richard H. Myers [États-Unis]State of the art review: Molecular diagnosis of inherited movement disorders. Movement Disorders Society task force on molecular diagnosis
002A19 (2003) Giovanni Defazio [Italie] ; Francesco Brancati [Italie] ; Enza Maria Valente [Italie] ; Viviana Caputo [Italie] ; Antonio Pizzuti [Italie] ; Davide Martino [Italie] ; Giovanni Abbruzzese [Italie] ; Paolo Livrea [Italie] ; Alfredo Berardelli [Italie] ; Bruno Dallapiccola [Italie]Familial blepharospasm is inherited as an autosomal dominant trait and relates to a novel unassigned gene
002C41 (2002) Anna Rita Bentivoglio [Italie] ; Mario Loi [Italie] ; Enza M. Valente [Italie] ; Tamara Ialongo [Italie] ; Pietro Tonali [Italie] ; Alberto Albanese [Italie]Phenotypic variability of DYT1‐PTD: Does the clinical spectrum include psychogenic dystonia?
002C61 (2002) Francesco Brancati [Italie] ; Giovanni Defazio [Italie] ; Viviana Caputo [Italie] ; Enza Maria Valente [Italie, Royaume-Uni] ; Antonio Pizzuti [Italie] ; Paolo Livrea [Italie] ; Alfredo Berardelli [Italie] ; Bruno Dallapiccola [Italie]Novel Italian family supports clinical and genetic heterogeneity of primary adult‐onset torsion dystonia

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