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Mutations in HPCA cause autosomal-recessive primary isolated dystonia.
Charlesworth G, Angelova PR, Bartolomé-Robledo F, Ryten M, Trabzuni D, Stamelou M, Abramov AY, Bhatia KP, Wood NW. Charlesworth G, et al. Among authors: stamelou m. Am J Hum Genet. 2015 Apr 2;96(4):657-65. doi: 10.1016/j.ajhg.2015.02.007. Epub 2015 Mar 19. Am J Hum Genet. 2015. PMID: 25799108 Free PMC article.
Treatment of focal dystonia.
Batla A, Stamelou M, Bhatia KP. Batla A, et al. Among authors: stamelou m. Curr Treat Options Neurol. 2012 Jun;14(3):213-29. doi: 10.1007/s11940-012-0169-6. Curr Treat Options Neurol. 2012. PMID: 22415705
Late onset rest-tremor in DYT1 dystonia.
Stamelou M, Edwards MJ, Bhatia KP. Stamelou M, et al. Parkinsonism Relat Disord. 2013 Jan;19(1):136-7. doi: 10.1016/j.parkreldis.2012.05.026. Epub 2012 Jun 19. Parkinsonism Relat Disord. 2013. PMID: 22721973 No abstract available.
Myoclonus-dystonia syndrome due to tyrosine hydroxylase deficiency.
Stamelou M, Mencacci NE, Cordivari C, Batla A, Wood NW, Houlden H, Hardy J, Bhatia KP. Stamelou M, et al. Neurology. 2012 Jul 31;79(5):435-41. doi: 10.1212/WNL.0b013e318261714a. Epub 2012 Jul 18. Neurology. 2012. PMID: 22815559 Free PMC article.
209 results