Bhatia KP - Search Results

1

PRRT2 gene mutations: from paroxysmal dyskinesia to episodic ataxia and hemiplegic migraine.

Gardiner AR, Bhatia KP, Stamelou M, Dale RC, Kurian MA, Schneider SA, Wali GM, Counihan T, Schapira AH, Spacey SD, Valente EM, Silveira-Moriyama L, Teive HA, Raskin S, Sander JW, Lees A, Warner T, Kullmann DM, Wood NW, Hanna M, Houlden H. Gardiner AR, et al. Among authors: bhatia kp. Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077024 Free PMC article.

2

Myoclonus-dystonia syndrome: epsilon-sarcoglycan mutations and phenotype.

Asmus F, Zimprich A, Tezenas Du Montcel S, Kabus C, Deuschl G, Kupsch A, Ziemann U, Castro M, Kühn AA, Strom TM, Vidailhet M, Bhatia KP, Dürr A, Wood NW, Brice A, Gasser T. Asmus F, et al. Among authors: bhatia kp. Ann Neurol. 2002 Oct;52(4):489-92. doi: 10.1002/ana.10325. Ann Neurol. 2002. PMID: 12325078

3

Slowly progressive cerebellar ataxia and cervical dystonia: clinical presentation of a new form of spinocerebellar ataxia?

Kuoppamäki M, Giunti P, Quinn N, Wood NW, Bhatia KP. Kuoppamäki M, et al. Among authors: bhatia kp. Mov Disord. 2003 Feb;18(2):200-6. doi: 10.1002/mds.10308. Mov Disord. 2003. PMID: 12539216 Review.

4

Parkin disease: a phenotypic study of a large case series.

Khan NL, Graham E, Critchley P, Schrag AE, Wood NW, Lees AJ, Bhatia KP, Quinn N. Khan NL, et al. Among authors: bhatia kp. Brain. 2003 Jun;126(Pt 6):1279-92. doi: 10.1093/brain/awg142. Brain. 2003. PMID: 12764051

5

Unusual phenotypes in DYT1 dystonia: a report of five cases and a review of the literature.

Edwards M, Wood N, Bhatia K. Edwards M, et al. Mov Disord. 2003 Jun;18(6):706-11. doi: 10.1002/mds.10411. Mov Disord. 2003. PMID: 12784278 Review.

6

Different patterns of electrophysiological deficits in manifesting and non-manifesting carriers of the DYT1 gene mutation.

Edwards MJ, Huang YZ, Wood NW, Rothwell JC, Bhatia KP. Edwards MJ, et al. Among authors: bhatia kp. Brain. 2003 Sep;126(Pt 9):2074-80. doi: 10.1093/brain/awg209. Epub 2003 Jun 23. Brain. 2003. PMID: 12821514

7

An unusual family with multiple movement disorders.

Edwards M, Russo N, Summers B, Morton J, Peake D, Bhatia K. Edwards M, et al. J Neurol. 2003 Jul;250(7):793-6. doi: 10.1007/s00415-003-1078-0. J Neurol. 2003. PMID: 12883919

8

Autosomal recessive, DYT2-like primary torsion dystonia: a new family.

Khan NL, Wood NW, Bhatia KP. Khan NL, et al. Among authors: bhatia kp. Neurology. 2003 Dec 23;61(12):1801-3. doi: 10.1212/01.wnl.0000099076.17187.9a. Neurology. 2003. PMID: 14694054

9

A functional polymorphism regulating dopamine beta-hydroxylase influences against Parkinson's disease.

Healy DG, Abou-Sleiman PM, Ozawa T, Lees AJ, Bhatia K, Ahmadi KR, Wullner U, Berciano J, Moller JC, Kamm C, Burk K, Barone P, Tolosa E, Quinn N, Goldstein DB, Wood NW. Healy DG, et al. Ann Neurol. 2004 Mar;55(3):443-6. doi: 10.1002/ana.20063. Ann Neurol. 2004. PMID: 14991826

10

Natural history and syndromic associations of orthostatic tremor: a review of 41 patients.

Gerschlager W, Münchau A, Katzenschlager R, Brown P, Rothwell JC, Quinn N, Lees AJ, Bhatia KP. Gerschlager W, et al. Among authors: bhatia kp. Mov Disord. 2004 Jul;19(7):788-795. doi: 10.1002/mds.20132. Mov Disord. 2004. PMID: 15254936

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