HuGE Literature Finder
Records 1-13
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A preliminary exome sequence in three patients with tardive dystonia.
Psychiatric genetics 2019 Dec . Kanahara Nobuhisa, Nakata Yusuke, Iyo Masao |
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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 |
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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 |
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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 |
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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 |
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Cognition and psychopathology in myoclonus-dystonia.
Journal of neurology, neurosurgery, and psychiatry 2012 Aug 83 (8): 814-20. van Tricht Mirjam J, Dreissen Yasmine E M, Cath Danielle, Dijk Joke M, Contarino Maria Fiorella, van der Salm Sandra M, Foncke Elisabeth M J, Groen Justus L, Schmand Ben, Tijssen Marina A |
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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 |
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Screening for dystonia genes DYT1, 11 and 16 in patients with writer's cramp.
Movement disorders : official journal of the Movement Disorder Society 2009 Jul 24 (9): 1390-2. Ritz Katja, Groen Justus L, Kruisdijk Jose J M, Baas Frank, Koelman Johannes H T M, Tijssen Marina A |
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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 |
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Clinical and molecular genetic evaluation of patients with primary dystonia.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2005 Feb 12 (2): 131-8. Shang H, Clerc N, Lang D, Kaelin-Lang A, Burgunder J |
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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 |
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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 |
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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 |
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- Page last updated:Apr 02, 2020
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