Wali GM - Search Results

1

Genetic and clinical heterogeneity in paroxysmal kinesigenic dyskinesia: evidence for a third EKD gene.

Spacey SD, Valente EM, Wali GM, Warner TT, Jarman PR, Schapira AH, Dixon PH, Davis MB, Bhatia KP, Wood NW. Spacey SD, et al. Among authors: wali gm. Mov Disord. 2002 Jul;17(4):717-25. doi: 10.1002/mds.10126. Mov Disord. 2002. PMID: 12210861

2

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: wali gm. Brain. 2000 Oct;123 ( Pt 10):2040-5. doi: 10.1093/brain/123.10.2040. Brain. 2000. PMID: 11004121

3

Mutation analysis of the sodium/hydrogen exchanger gene (NHE5) in familial paroxysmal kinesigenic dyskinesia.

Spacey SD, Szczygielski BI, McRory JE, Wali GM, Wood NW, Snutch TP. Spacey SD, et al. Among authors: wali gm. J Neural Transm (Vienna). 2002 Sep;109(9):1189-94. doi: 10.1007/s00702-002-0750-3. J Neural Transm (Vienna). 2002. PMID: 12203045

4

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: wali gm. Neurology. 2012 Nov 20;79(21):2115-21. doi: 10.1212/WNL.0b013e3182752c5a. Epub 2012 Oct 17. Neurology. 2012. PMID: 23077024 Free PMC article.

5

Shoulder girdle dyskinesia following local surgery.

Wali GM. Wali GM. Mov Disord. 1999 Nov;14(6):1051-3. doi: 10.1002/1531-8257(199911)14:6<1051::aid-mds1030>3.0.co;2-j. Mov Disord. 1999. PMID: 10584692 No abstract available.

6

Shoulder girdle dyskinesia associated with a thalamic infarct.

Wali GM. Wali GM. Mov Disord. 1999 Mar;14(2):375-7. doi: 10.1002/1531-8257(199903)14:2<375::aid-mds1033>3.0.co;2-s. Mov Disord. 1999. PMID: 10091642 No abstract available.

7

Asymmetrical blepharospasm associated with a left frontal cortical infarct.

Wali GM. Wali GM. Mov Disord. 2001 Jan;16(1):181-2. doi: 10.1002/1531-8257(200101)16:1<181::aid-mds1036>3.0.co;2-c. Mov Disord. 2001. PMID: 11215588 No abstract available.

8

Friedreich ataxia associated with dystonic head tremor provoked by prolonged exercise.

Wali GM. Wali GM. Mov Disord. 2000 Nov;15(6):1298-9. doi: 10.1002/1531-8257(200011)15:6<1298::aid-mds1049>3.0.co;2-9. Mov Disord. 2000. PMID: 11104234 No abstract available.

9

Sepiapterin reductase deficiency: two Indian siblings with unusual clinical features.

Wali GM, Thony B, Blau N. Wali GM, et al. Mov Disord. 2010 May 15;25(7):954-5. doi: 10.1002/mds.23032. Mov Disord. 2010. PMID: 20222129 No abstract available.

10

Whole genome sequencing for the genetic diagnosis of heterogenous dystonia phenotypes.

Kumar KR, Davis RL, Tchan MC, Wali GM, Mahant N, Ng K, Kotschet K, Siow SF, Gu J, Walls Z, Kang C, Wali G, Levy S, Phua CS, Yiannikas C, Darveniza P, Chang FCF, Morales-Briceño H, Rowe DB, Drew A, Gayevskiy V, Cowley MJ, Minoche AE, Tisch S, Hayes M, Kummerfeld S, Fung VSC, Sue CM. Kumar KR, et al. Among authors: wali gm. Parkinsonism Relat Disord. 2019 Dec;69:111-118. doi: 10.1016/j.parkreldis.2019.11.004. Epub 2019 Nov 7. Parkinsonism Relat Disord. 2019. PMID: 31731261 Free article.

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