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The CACNA1B R1389H variant is not associated with myoclonus-dystonia in a large European multicentric cohort.
Mencacci NE, R'bibo L, Bandres-Ciga S, Carecchio M, Zorzi G, Nardocci N, Garavaglia B, Batla A, Bhatia KP, Pittman AM, Hardy J, Weissbach A, Klein C, Gasser T, Lohmann E, Wood NW. Mencacci NE, et al. Among authors: batla a. Hum Mol Genet. 2015 Sep 15;24(18):5326-9. doi: 10.1093/hmg/ddv255. Epub 2015 Jul 8. Hum Mol Genet. 2015. PMID: 26157024 Free PMC article.
Treatment of focal dystonia.
Batla A, Stamelou M, Bhatia KP. Batla A, et al. Curr Treat Options Neurol. 2012 Jun;14(3):213-29. doi: 10.1007/s11940-012-0169-6. Curr Treat Options Neurol. 2012. PMID: 22415705
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. Among authors: batla a. Neurology. 2012 Jul 31;79(5):435-41. doi: 10.1212/WNL.0b013e318261714a. Epub 2012 Jul 18. Neurology. 2012. PMID: 22815559 Free PMC article.
Markedly asymmetric presentation in multiple system atrophy.
Batla A, Stamelou M, Mensikova K, Kaiserova M, Tuckova L, Kanovsky P, Quinn N, Bhatia KP. Batla A, et al. Parkinsonism Relat Disord. 2013 Oct;19(10):901-5. doi: 10.1016/j.parkreldis.2013.05.004. Epub 2013 Jun 6. Parkinsonism Relat Disord. 2013. PMID: 23746453
Psychogenic paroxysmal movement disorders--clinical features and diagnostic clues.
Ganos C, Aguirregomozcorta M, Batla A, Stamelou M, Schwingenschuh P, Münchau A, Edwards MJ, Bhatia KP. Ganos C, et al. Among authors: batla a. Parkinsonism Relat Disord. 2014 Jan;20(1):41-6. doi: 10.1016/j.parkreldis.2013.09.012. Epub 2013 Sep 19. Parkinsonism Relat Disord. 2014. PMID: 24090947 Free article.
Rest and other types of tremor in adult-onset primary dystonia.
Erro R, Rubio-Agusti I, Saifee TA, Cordivari C, Ganos C, Batla A, Bhatia KP. Erro R, et al. Among authors: batla a. J Neurol Neurosurg Psychiatry. 2014 Sep;85(9):965-8. doi: 10.1136/jnnp-2013-305876. Epub 2013 Nov 18. J Neurol Neurosurg Psychiatry. 2014. PMID: 24249781 Free PMC article.
A new gene for Fahr's syndrome-PDGF-B.
Batla A, Bhatia KP. Batla A, et al. Mov Disord. 2014 Mar;29(3):307. doi: 10.1002/mds.25788. Epub 2014 Jan 3. Mov Disord. 2014. PMID: 24390807 No abstract available.
87 results