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Journal of the Neurological Sciences|January 21, 2014
Physical precipitating factors in functional movement disordersIsabel Pareés, Maja Kojovic, Carolina Pires, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 13, 2013
Movement disorders in adult patients with classical galactosemiaIgnacio Rubio-Agusti, Miryam Carecchio, Kailash P Bhatia, et al.American Journal of Human Genetics|December 4, 2012
Mutations in ANO3 cause dominant craniocervical dystonia: ion channel implicated in pathogenesisGavin Charlesworth, Vincent Plagnol, Kira M Holmström, et al.Movement Disorders : Official Journal of the Movement Disorder Society|February 19, 2013
The syndrome of deafness-dystonia: clinical and genetic heterogeneityMaja Kojovic, Isabel Pareés, Tania Lampreia, et al.American Journal of Human Genetics|May 19, 2015
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaNiccolo E Mencacci, Ignacio Rubio-Agusti, Anselm Zdebik, et al.Movement Disorders : Official Journal of the Movement Disorder Society|September 27, 2014
Lack of validation of variants associated with cervical dystonia risk: a GWAS replication studyPilar Gómez-Garre, Ismael Huertas-Fernández, María Teresa Cáceres-Redondo, et al.Pageof 2