Movement Disorders (genetics) And NotPierre Payoux

List of bibliographic references

Number of relevant bibliographic references: 6.

Ident.	Authors (with country if any)	Title
000172	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	Kiyoka Kinugawa [France] ; Marie Vidailhet [France] ; Fabienne Clot [France] ; Emmanuelle Apartis [France] ; David Grabli [France] ; Emmanuel Roze [France]	Myoclonus‐dystonia: An update
000446	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	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	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	Tanya Stojkovic [France] ; Luc Defebvre [France] ; Xavier Quilliet ; Eric Eveno ; Alain Sarasin ; Mauro Mezzina ; Destée	Neurological manifestations in two related xeroderma pigmentosum group d patients: Complications of the late‐onset type of the juvenile form

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