SGCE mutations cause psychiatric disorders: clinical and genetic characterization
about
A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystoniaTreatment of myoclonus-dystonia syndrome with tetrabenazine.Distribution and Coexistence of Myoclonus and Dystonia as Clinical Predictors of SGCE Mutation Status: A Pilot Study.Functional dystonia and the borderland between neurology and psychiatry: New concepts.A guide to childhood motor stereotypies, tic disorders and the tourette spectrum for the primary care practitioner.Genetics of dystonia: what's known? What's new? What's next?SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotype.Long-term neuropsychiatric outcomes after pallidal stimulation in primary and secondary dystonia.Psychiatric disorders, myoclonus dystonia and SGCE: an international studyNew Perspectives on Genomic Imprinting, an Essential and Multifaceted Mode of Epigenetic Control in the Developing and Adult Brain.Nonmotor symptoms in primary adult-onset cervical dystonia and blepharospasmPrimary and secondary dystonic syndromes: an update.The genetics of dystonia: new twists in an old tale.Understanding dystonia: diagnostic issues and how to overcome them.Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome.A History of Dystonia: Ancient to ModernMyoclonus dystonia and muscular dystrophy: ɛ-sarcoglycan is part of the dystrophin-associated protein complex in brain.Low CSF 5-HIAA in Myoclonus Dystonia.Associations of specific psychiatric disorders with isolated focal dystonia, and monogenic and idiopathic Parkinson's disease.Unusual α-synuclein and cerebellar pathologies in a case of hereditary myoclonus-dystonia without SGCE mutation.Pallidal stimulation for myoclonus-dystonia: Ten years' outcome in two patients.Bilateral pallidal deep brain stimulation in myoclonus-dystonia: our experience in three cases and their follow-up.Benign hereditary chorea related to NKX2.1: expansion of the genotypic and phenotypic spectrum.Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria.Dystonia.Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation.Effects of insulin-like growth factor binding protein 3 on apoptosis of cutaneous squamous cell carcinoma cells
P2860
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P2860
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
description
2013 nî lūn-bûn
@nan
2013 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@ast
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@en
type
label
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@ast
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@en
prefLabel
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@ast
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@en
P2093
P2860
P50
P356
P1433
P1476
SGCE mutations cause psychiatric disorders: clinical and genetic characterization
@en
P2093
Andrew Lux
Bryan Lynch
Cathy White
Daniel J Smith
Derek J Blake
Hardev Pall
Kathryn J Peall
Manju A Kurian
Martin Smith
Mary D King
P2860
P304
P356
10.1093/BRAIN/AWS308
P407
P577
2013-01-01T00:00:00Z