Bhatia KP - Search Results

1

Paroxysmal Kinesigenic Dyskinesia May Be Misdiagnosed in Co-occurring Gilles de la Tourette Syndrome.

Ganos C, Mencacci N, Gardiner A, Erro R, Batla A, Houlden H, Bhatia KP. Ganos C, et al. Among authors: bhatia kp. Mov Disord Clin Pract. 2014 Apr 10;1(1):84-86. doi: 10.1002/mdc3.12001. eCollection 2014 Apr. Mov Disord Clin Pract. 2014. PMID: 30363829 Free PMC article. No abstract available.

2

Characterization of PLA2G6 as a locus for dystonia-parkinsonism.

Paisan-Ruiz C, Bhatia KP, Li A, Hernandez D, Davis M, Wood NW, Hardy J, Houlden H, Singleton A, Schneider SA. Paisan-Ruiz C, et al. Among authors: bhatia kp. Ann Neurol. 2009 Jan;65(1):19-23. doi: 10.1002/ana.21415. Ann Neurol. 2009. PMID: 18570303 Free PMC article.

3

A common polymorphism in the brain-derived neurotrophic factor gene (BDNF) modulates human cortical plasticity and the response to rTMS.

Cheeran B, Talelli P, Mori F, Koch G, Suppa A, Edwards M, Houlden H, Bhatia K, Greenwood R, Rothwell JC. Cheeran B, et al. J Physiol. 2008 Dec 1;586(23):5717-25. doi: 10.1113/jphysiol.2008.159905. Epub 2008 Oct 9. J Physiol. 2008. PMID: 18845611 Free PMC article. Clinical Trial.

4

ATP13A2 mutations (PARK9) cause neurodegeneration with brain iron accumulation.

Schneider SA, Paisan-Ruiz C, Quinn NP, Lees AJ, Houlden H, Hardy J, Bhatia KP. Schneider SA, et al. Among authors: bhatia kp. Mov Disord. 2010 Jun 15;25(8):979-84. doi: 10.1002/mds.22947. Mov Disord. 2010. PMID: 20310007

5

Widespread Lewy body and tau accumulation in childhood and adult onset dystonia-parkinsonism cases with PLA2G6 mutations.

Paisán-Ruiz C, Li A, Schneider SA, Holton JL, Johnson R, Kidd D, Chataway J, Bhatia KP, Lees AJ, Hardy J, Revesz T, Houlden H. Paisán-Ruiz C, et al. Among authors: bhatia kp. Neurobiol Aging. 2012 Apr;33(4):814-23. doi: 10.1016/j.neurobiolaging.2010.05.009. Epub 2010 Jul 21. Neurobiol Aging. 2012. PMID: 20619503 Free PMC article.

6

Indian-subcontinent NBIA: unusual phenotypes, novel PANK2 mutations, and undetermined genetic forms.

Aggarwal A, Schneider SA, Houlden H, Silverdale M, Paudel R, Paisan-Ruiz C, Desai S, Munshi M, Sanghvi D, Hardy J, Bhatia KP, Bhatt M. Aggarwal A, et al. Among authors: bhatia kp. Mov Disord. 2010 Jul 30;25(10):1424-31. doi: 10.1002/mds.23095. Mov Disord. 2010. PMID: 20629144

7

Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutations.

Paisán-Ruiz C, Guevara R, Federoff M, Hanagasi H, Sina F, Elahi E, Schneider SA, Schwingenschuh P, Bajaj N, Emre M, Singleton AB, Hardy J, Bhatia KP, Brandner S, Lees AJ, Houlden H. Paisán-Ruiz C, et al. Among authors: bhatia kp. Mov Disord. 2010 Sep 15;25(12):1791-800. doi: 10.1002/mds.23221. Mov Disord. 2010. PMID: 20669327 Free PMC article.

8

Paroxysmal dyskinesias.

Bhatia KP. Bhatia KP. Mov Disord. 2011 May;26(6):1157-65. doi: 10.1002/mds.23765. Mov Disord. 2011. PMID: 21626559 Review.

9

Treatment of focal dystonia.

Batla A, Stamelou M, Bhatia KP. Batla A, et al. Among authors: bhatia kp. Curr Treat Options Neurol. 2012 Jun;14(3):213-29. doi: 10.1007/s11940-012-0169-6. Curr Treat Options Neurol. 2012. PMID: 22415705

10

Joint hypermobility syndrome: a risk factor for fixed dystonia?

Kassavetis P, Batla A, Pareés I, Saifee TA, Schrag A, Cordivari C, Bhatia KP, Edwards MJ. Kassavetis P, et al. Among authors: bhatia kp. Mov Disord. 2012 Jul;27(8):1070. doi: 10.1002/mds.25004. Epub 2012 Apr 24. Mov Disord. 2012. PMID: 22532260 No abstract available.

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