Opal P - Search Results

1

Intrafamilial phenotypic variability of the DYT1 dystonia: from asymptomatic TOR1A gene carrier status to dystonic storm.

Opal P, Tintner R, Jankovic J, Leung J, Breakefield XO, Friedman J, Ozelius L. Opal P, et al. Mov Disord. 2002 Mar;17(2):339-45. doi: 10.1002/mds.10096. Mov Disord. 2002. PMID: 11921121

2

Spinocerebellar ataxia type 1: It's not just about Purkinje cells.

Opal P. Opal P. Neuron. 2023 Aug 16;111(16):2461-2462. doi: 10.1016/j.neuron.2023.07.014. Neuron. 2023. PMID: 37591199 Free article.

3

Adapting to post-COVID19 research in Parkinson's disease: Lessons from a multinational experience.

Tan EK, Albanese A, Chaudhuri K, Lim SY, Oey NE, Shan Chan CH, Wu YC, Jeon B, Truong D, Poewe W, Pal PK, Tan L, Opal P, Colosimo C, Jinnah HA, Cardoso F. Tan EK, et al. Among authors: opal p. Parkinsonism Relat Disord. 2021 Jan;82:146-149. doi: 10.1016/j.parkreldis.2020.10.009. Epub 2020 Oct 7. Parkinsonism Relat Disord. 2021. PMID: 33071183 Free PMC article. Review. No abstract available.

4

Standards of Fluid Biomarker Collection and Pre-analytical Processes in Humans and Mice: Recommendations by the Ataxia Global Initiative Working Group on Biomarkers.

Santorelli FM, McLoughlin HS, Wolter JM, Galatolo D, Synofzik M, Mengel D, Opal P; AGI-WG2-Biomarkers Study Group. Santorelli FM, et al. Among authors: opal p. Cerebellum. 2024 Jun;23(3):881-886. doi: 10.1007/s12311-023-01561-1. Epub 2023 May 27. Cerebellum. 2024. PMID: 37243885

5

Neurological research & training after the easing of lockdown in countries impacted by COVID-19.

Tan EK, Albanese A, Chaudhuri KR, Opal P, Wu YC, Chan CH, Jeon B, Truong D, Poewe W, Tan L, Pal P, Colosimo C, Lim SY, Jinnah HA, Cardoso F. Tan EK, et al. Among authors: opal p. J Neurol Sci. 2020 Nov 15;418:117105. doi: 10.1016/j.jns.2020.117105. Epub 2020 Aug 24. J Neurol Sci. 2020. PMID: 32980781 Free PMC article. No abstract available.

6

The role of chaperones in polyglutamine disease.

Opal P, Zoghbi HY. Opal P, et al. Trends Mol Med. 2002 May;8(5):232-6. doi: 10.1016/s1471-4914(02)02310-9. Trends Mol Med. 2002. PMID: 12067633 Review.

7

Huntington's disease presenting as postsurgical psychosis.

Paganoni S, Naidech AM, Opal P. Paganoni S, et al. Among authors: opal p. Mov Disord. 2007 Jun 15;22(8):1209-10. doi: 10.1002/mds.21522. Mov Disord. 2007. PMID: 17443707 No abstract available.

8

Developmental Alterations in Adult-Onset Neurodegenerative Disorders: Lessons from Polyglutamine Diseases.

Edamakanti CR, Opal P. Edamakanti CR, et al. Among authors: opal p. Mov Disord. 2021 Jul;36(7):1548-1552. doi: 10.1002/mds.28657. Epub 2021 May 20. Mov Disord. 2021. PMID: 34014004 Free PMC article. No abstract available.

9

Loss of the dystonia gene Thap1 leads to transcriptional deficits that converge on common pathogenic pathways in dystonic syndromes.

Frederick NM, Shah PV, Didonna A, Langley MR, Kanthasamy AG, Opal P. Frederick NM, et al. Among authors: opal p. Hum Mol Genet. 2019 Apr 15;28(8):1343-1356. doi: 10.1093/hmg/ddy433. Hum Mol Genet. 2019. PMID: 30590536 Free PMC article.

10

Over-expression of inducible HSP70 chaperone suppresses neuropathology and improves motor function in SCA1 mice.

Cummings CJ, Sun Y, Opal P, Antalffy B, Mestril R, Orr HT, Dillmann WH, Zoghbi HY. Cummings CJ, et al. Among authors: opal p. Hum Mol Genet. 2001 Jul 1;10(14):1511-8. doi: 10.1093/hmg/10.14.1511. Hum Mol Genet. 2001. PMID: 11448943

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