Familial congenital mirror movements: report of a ... [Neurology. 2009] - PubMed

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An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus? [Neurology. 2005]
An autosomal dominant ataxia maps to 19q13: Allelic heterogeneity of SCA13 or novel locus?
Waters MF, Fee D, Figueroa KP, Nolte D, Müller U, Advincula J, Coon H, Evidente VG, Pulst SM. Neurology. 2005 Oct 11; 65(7):1111-3. Epub 2005 Aug 31.
TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome. [Neurology. 2008]
TNFRSF1A R92Q mutation in association with a multiple sclerosis-like demyelinating syndrome.
Hoffmann LA, Lohse P, König FB, Feneberg W, Hohlfeld R, Kümpfel T. Neurology. 2008 Mar 25; 70(13 Pt 2):1155-6. Epub 2008 Feb 20.
Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis. [Acta Neurol Scand. 2005]
Autosomal dominant cerebellar ataxias in Spain: molecular and clinical correlations, prevalence estimation and survival analysis.
Infante J, Combarros O, Volpini V, Corral J, Llorca J, Berciano J. Acta Neurol Scand. 2005 Jun; 111(6):391-9.
Review [Stereotypic movements]. [Rev Neurol. 2003]
Review [Stereotypic movements].
Fernández-Alvarez E. Rev Neurol. 2003 Feb; 36 Suppl 1:S54-6.
Review Motor stereotypies. [Semin Pediatr Neurol. 2009]
Review Motor stereotypies.
Singer HS. Semin Pediatr Neurol. 2009 Jun; 16(2):77-81.

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