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Movement Disorders (revue) - Analysis (France)

Index « Keywords » - entrée « Movement Disorders (genetics) »
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Movement Disorders (etiology) < Movement Disorders (genetics) < Movement Disorders (metabolism)  Facettes :

List of bibliographic references

Number of relevant bibliographic references: 7.
Ident.Authors (with country if any)Title
000172 (2011) Marie Chauveau [France] ; Nathalie Damon-Perriere [France] ; Chrystelle Latxague [France] ; Umberto Spampinato [France] ; Hans Jung [Suisse] ; Pierre Burbaud [France] ; François Tison [France]Head drops are also observed in McLeod syndrome
000244 (2009) Kiyoka Kinugawa [France] ; Marie Vidailhet [France] ; Fabienne Clot [France] ; Emmanuelle Apartis [France] ; David Grabli [France] ; Emmanuel Roze [France]Myoclonus‐dystonia: An update
000262 (2009) Fabienne Ory-Magne [France] ; Christine Brefel-Courbon [France] ; Pierre Payoux [France] ; Sabrina Debruxelles [France] ; Igor Sibon [France] ; Cyril Goizet [France] ; Pierre Labauge [France] ; Patrice Menegon [France] ; Emmanuelle Uro-Coste [France] ; Bernardino Ghetti [États-Unis] ; Marie Bernadetle Delisle [France] ; Ruben Vidal [États-Unis] ; Olivier Rascol [France]Clinical phenotype and neuroimaging findings in a French family with hereditary ferritinopathy (FTL498‐499InsTC)
000446 (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
000521 (2000) Alain Destée [France] ; Isabelle Delalande [France] ; Isabelle Vuillaume [France] ; Susanna Schraen-Maschke [France] ; Luc Defebvre [France] ; Bernard Sablonnière [France]The first identified French family with dentatorubral‐pallidoluysian atrophy
000529 (2000) G. Demarquay [France] ; A. Setiey [France] ; Y. Morel [France] ; C. Trepo [France] ; G. Chazot [France] ; E. Broussolle [France]Clinical report of three patients with hereditary hemochromatosis and movement disorders
000586 (1997) Tanya Stojkovic [France] ; Luc Defebvre [France] ; Xavier Quilliet ; Eric Eveno ; Alain Sarasin ; Mauro Mezzina ; DestéeNeurological manifestations in two related xeroderma pigmentosum group d patients: Complications of the late‐onset type of the juvenile form

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