Bhatia KP - Search Results

1

Autosomal dominant cerebellar ataxia: SCA2 is the most frequent mutation in eastern India.

Sinha KK, Worth PF, Jha DK, Sinha S, Stinton VJ, Davis MB, Wood NW, Sweeney MG, Bhatia KP. Sinha KK, et al. Among authors: bhatia kp. J Neurol Neurosurg Psychiatry. 2004 Mar;75(3):448-52. doi: 10.1136/jnnp.2002.004895. J Neurol Neurosurg Psychiatry. 2004. PMID: 14966163 Free PMC article.

2

Phenotypic homogeneity of the Huntington disease-like presentation in a SCA17 family.

Schneider SA, van de Warrenburg BP, Hughes TD, Davis M, Sweeney M, Wood N, Quinn NP, Bhatia KP. Schneider SA, et al. Among authors: bhatia kp. Neurology. 2006 Nov 14;67(9):1701-3. doi: 10.1212/01.wnl.0000242740.01273.00. Neurology. 2006. PMID: 17101913

3

Autosomal-dominant GTPCH1-deficient DRD: clinical characteristics and long-term outcome of 34 patients.

Trender-Gerhard I, Sweeney MG, Schwingenschuh P, Mir P, Edwards MJ, Gerhard A, Polke JM, Hanna MG, Davis MB, Wood NW, Bhatia KP. Trender-Gerhard I, et al. Among authors: bhatia kp. J Neurol Neurosurg Psychiatry. 2009 Aug;80(8):839-45. doi: 10.1136/jnnp.2008.155861. Epub 2009 Mar 29. J Neurol Neurosurg Psychiatry. 2009. PMID: 19332422

4

Tau gene and Parkinson's disease: a case-control study and meta-analysis.

Healy DG, Abou-Sleiman PM, Lees AJ, Casas JP, Quinn N, Bhatia K, Hingorani AD, Wood NW. Healy DG, et al. J Neurol Neurosurg Psychiatry. 2004 Jul;75(7):962-5. doi: 10.1136/jnnp.2003.026203. J Neurol Neurosurg Psychiatry. 2004. PMID: 15201350 Free PMC article.

5

The role of DYT1 in primary torsion dystonia in Europe.

Valente EM, Warner TT, Jarman PR, Mathen D, Fletcher NA, Marsden CD, Bhatia KP, Wood NW. Valente EM, et al. Among authors: bhatia kp. Brain. 1998 Dec;121 ( Pt 12):2335-9. doi: 10.1093/brain/121.12.2335. Brain. 1998. PMID: 9874484

6

A new family with paroxysmal exercise induced dystonia and migraine: a clinical and genetic study.

Münchau A, Valente EM, Shahidi GA, Eunson LH, Hanna MG, Quinn NP, Schapira AH, Wood NW, Bhatia KP. Münchau A, et al. Among authors: bhatia kp. J Neurol Neurosurg Psychiatry. 2000 May;68(5):609-14. doi: 10.1136/jnnp.68.5.609. J Neurol Neurosurg Psychiatry. 2000. PMID: 10766892 Free PMC article.

7

A second paroxysmal kinesigenic choreoathetosis locus (EKD2) mapping on 16q13-q22.1 indicates a family of genes which give rise to paroxysmal disorders on human chromosome 16.

Valente EM, Spacey SD, Wali GM, Bhatia KP, Dixon PH, Wood NW, Davis MB. Valente EM, et al. Among authors: bhatia kp. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

8

A Yorkshire family with adult-onset cranio-cervical primary torsion dystonia.

Münchau A, Valente EM, Davis MB, Stinton V, Wood NW, Quinn NP, Bhatia KP. Münchau A, et al. Among authors: bhatia kp. Mov Disord. 2000 Sep;15(5):954-9. doi: 10.1002/1531-8257(200009)15:5<954::aid-mds1028>3.0.co;2-i. Mov Disord. 2000. PMID: 11009204

9

Cervical dystonia is associated with a polymorphism in the dopamine (D5) receptor gene.

Placzek MR, Misbahuddin A, Chaudhuri KR, Wood NW, Bhatia KP, Warner TT. Placzek MR, et al. Among authors: bhatia kp. J Neurol Neurosurg Psychiatry. 2001 Aug;71(2):262-4. doi: 10.1136/jnnp.71.2.262. J Neurol Neurosurg Psychiatry. 2001. PMID: 11459908 Free PMC article.

10

Familial adult onset of Krabbe's disease resembling hereditary spastic paraplegia with normal neuroimaging.

Bajaj NP, Waldman A, Orrell R, Wood NW, Bhatia KP. Bajaj NP, et al. Among authors: bhatia kp. J Neurol Neurosurg Psychiatry. 2002 May;72(5):635-8. doi: 10.1136/jnnp.72.5.635. J Neurol Neurosurg Psychiatry. 2002. PMID: 11971051 Free PMC article.

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