Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Public Health Genomics and Precision Health Knowledge Base (v7.2)

Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page: About CDC.gov.

HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-10

Query Trace: Dystonia and SGCE[original query]

A preliminary exome sequence in three patients with tardive dystonia. Psychiatric genetics 2019 Dec . Kanahara Nobuhisa, Nakata Yusuke, Iyo Masao Similar articles in PubMed
Psychiatric disorders, myoclonus dystonia and SGCE: an international study. Annals of clinical and translational neurology 2016 Jan 3 (1): 4-11. Peall Kathryn J, Dijk Joke M, Saunders-Pullman Rachel, Dreissen Yasmine E M, van Loon Ilke, Cath Danielle, Kurian Manju A, Owen Michael J, Foncke Elisabeth M J, Morris Huw R, Gasser Thomas, Bressman Susan, Asmus Friedrich, Tijssen Marina A Similar articles in PubMed
Han Chinese patients with dopa-responsive dystonia exhibit a low frequency of exonic deletion in the GCH1 gene. Genetics and molecular research : GMR 2015 14 (3): 11185-90. Shi W T, Cai C Y, Li M S, Ling C, Li W Similar articles in PubMed
Defining the epsilon-sarcoglycan (SGCE) gene phenotypic signature in myoclonus-dystonia: a reappraisal of genetic testing criteria. Movement disorders : official journal of the Movement Disorder Society 2013 Jun 28 (6): 787-94. Carecchio Miryam, Magliozzi Monia, Copetti Massimiliano, Ferraris Alessandro, Bernardini Laura, Bonetti Monica, Defazio Giovanni, Edwards Mark J, Torrente Isabella, Pellegrini Fabio, Comi Cristoforo, Bhatia Kailash P, Valente Enza Mar Similar articles in PubMed
SGCE mutations cause psychiatric disorders: clinical and genetic characterization. Brain : a journal of neurology 2013 Jan 136 (Pt 1): Pt 1. Peall KJ, Smith DJ, Kurian MA, Wardle M, Waite AJ, Hedderly T, Lin JP, Smith M, Whone A, Pall H, White C, Lux A, Jardine P, Bajaj N, Lynch B, Kirov G, O'Riordan S, Samuel M, Lynch T, King MD, Chinnery PF, Warner TT, Blake DJ, Owen MJ, Morris HR Similar articles in PubMed
Common polymorphisms in dystonia-linked genes and susceptibility to the sporadic primary dystonias. Parkinsonism & related disorders 2012 May 18 (4): 351-7. Newman Jeremy R B, Sutherland Greg T, Boyle Richard S, Limberg Nicole, Blum Stefan, O'Sullivan John D, Silburn Peter A, Mellick George Similar articles in PubMed
Myoclonus-dystonia: clinical and genetic evaluation of a large cohort. Journal of neurology, neurosurgery, and psychiatry 2009 Jun 80 (6): 653-8. Ritz K, Gerrits M C F, Foncke E M J, van Ruissen F, van der Linden C, Vergouwen M D I, Bloem B R, Vandenberghe W, Crols R, Speelman J D, Baas F, Tijssen M A Similar articles in PubMed
The epsilon-sarcoglycan gene in myoclonic syndromes. Neurology 2005 Feb 64 (4): 737-9. Valente E M, Edwards M J, Mir P, DiGiorgio A, Salvi S, Davis M, Russo N, Bozi M, Kim H-T, Pennisi G, Quinn N, Dallapiccola B, Bhatia K Similar articles in PubMed
Lack of mutations in the epsilon-sarcoglycan gene in patients with different subtypes of primary dystonias. Movement disorders : official journal of the Movement Disorder Society 2004 Nov 19 (11): 1294-7. Grundmann Kathrin, Laubis-Herrmann Ulrike, Dressler Dirk, Vollmer-Haase Juliane, Bauer Peter, Stuhrmann Manfred, Schulte Thorsten, Schöls Ludger, Topka Helge, Riess Ol Similar articles in PubMed
Examination of the SGCE gene in Tourette syndrome patients with obsessive-compulsive disorder. Movement disorders : official journal of the Movement Disorder Society 2004 Oct 19 (10): 1237-8. de Carvalho Aguiar Patricia, Fazzari Melissa, Jankovic Joseph, Ozelius Laurie Similar articles in PubMed

File Formats Help:

How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?

Page last reviewed:Oct 1, 2020
Page last updated:Mar 05, 2021
Content source:

TOP