DNA Mutational Analysis And NotAlexis Brice

List of bibliographic references

Number of relevant bibliographic references: 9.

Ident.	Authors (with country if any)	Title
000214	Paola S. Denora [France, Italie] ; Knut Brockmann [Allemagne] ; Marianna Ciccolella [Italie] ; Jeremy Truchetto [France] ; Giovanni Stevanin [France, Italie] ; Filippo M. Santorelli [Italie]	Identification of a de novo mutation in SPG11
000284	Amir Glik [Israël] ; Isabelle Vuillaume [France] ; David Devos [France] ; Rivka Inzelberg [Israël]	Psychosis, short stature in benign hereditary chorea: A novel thyroid transcription factor‐1 mutation
000291	Christoph Globas [Allemagne] ; Sophie Tezenas Du Montcel [France] ; Laslo Baliko [Hongrie] ; Syliva Boesch [Autriche] ; Chantal Depondt [Belgique] ; Stefano Didonato [Italie] ; Alexandra Durr [France] ; Alessandro Filla [Italie] ; Thomas Klockgether [Allemagne] ; Caterina Mariotti [Italie] ; Bela Melegh [Hongrie] ; Maryla Rakowicz [Pologne] ; Pascale Ribai [France] ; Rafal Rola [Pologne] ; Tanja Schmitz-Hubsch [Allemagne] ; Sandra Szymanski [Allemagne] ; Dagmar Timmann [Allemagne] ; Bart P. Van De Warrenburg [Pays-Bas] ; Peter Bauer [Allemagne] ; Ludger Schols [Allemagne]	Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6
000410	Claire-Marie Dhaenens [France] ; Pierre Krystkowiak [France] ; Xavier Douay [France] ; Pierre Charpentier [France] ; Sylvain Bele [France] ; Alain Destée [France] ; Bernard Sablonnière [France]	Clinical and genetic evaluation in a French population presenting with primary focal dystonia
000418	Morgane Caer [France] ; Karine Viala [France] ; Richard Levy [France] ; Thierry Maisonobe [France] ; Florence Chochon [France] ; Agnès Lombès [France] ; Yves Agid [France]	Adult‐onset chorea and mitochondrial cytopathy
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
000550	Patrick Chariot [France] ; Pierre Brugières [France] ; Marie-Christine Eliezer-Vanerot [France] ; Christian Gény [France] ; Michel Binaghi [France] ; Pierre Césaro [France]	Choreic movements and MRI abnormalities in the subthalamic nuclei reversible after administration of coenzyme Q10 and multiple vitamins in a patient with bilateral optic neuropathy
000631	Gilles Fénelon [France] ; Annaék Fève [France] ; Avindra Nath [Canada] ; Douglas E. Hobson [Canada] ; A. H. V. Schapira [Royaume-Uni] ; C. D. Marsden [Royaume-Uni] ; M. S. Sandy [États-Unis] ; J. W. Langston [États-Unis] ; D. A. Di Monte [États-Unis] ; James J. Gaul [États-Unis]	Letters to the editor

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