Fung V - Search Results

1

Comprehensive genetic diagnosis of tandem repeat expansion disorders with programmable targeted nanopore sequencing.

Stevanovski I, Chintalaphani SR, Gamaarachchi H, Ferguson JM, Pineda SS, Scriba CK, Tchan M, Fung V, Ng K, Cortese A, Houlden H, Dobson-Stone C, Fitzpatrick L, Halliday G, Ravenscroft G, Davis MR, Laing NG, Fellner A, Kennerson M, Kumar KR, Deveson IW. Stevanovski I, et al. Among authors: fung v. Sci Adv. 2022 Mar 4;8(9):eabm5386. doi: 10.1126/sciadv.abm5386. Epub 2022 Mar 4. Sci Adv. 2022. PMID: 35245110 Free PMC article.

2

Postmortem analysis of bilateral subthalamic electrode implants in Parkinson's disease.

Henderson JM, Pell M, O'Sullivan DJ, McCusker EA, Fung VS, Hedges P, Halliday GM. Henderson JM, et al. Mov Disord. 2002 Jan;17(1):133-7. doi: 10.1002/mds.1261. Mov Disord. 2002. PMID: 11835450

3

Facial nerve palsy after intracisternal papaverine application during aneurysm surgery--case report.

Lang EW, Neugebauer M, Ng K, Fung V, Clouston P, Dorsch NW. Lang EW, et al. Among authors: fung v. Neurol Med Chir (Tokyo). 2002 Dec;42(12):565-7. doi: 10.2176/nmc.42.565. Neurol Med Chir (Tokyo). 2002. PMID: 12513030 Free article.

4

Familial paroxysmal exercise-induced dystonia: atypical presentation of autosomal dominant GTP-cyclohydrolase 1 deficiency.

Dale RC, Melchers A, Fung VS, Grattan-Smith P, Houlden H, Earl J. Dale RC, et al. Dev Med Child Neurol. 2010 Jun;52(6):583-6. doi: 10.1111/j.1469-8749.2010.03619.x. Epub 2010 Feb 19. Dev Med Child Neurol. 2010. PMID: 20187889 Free article.

5

Cortical limb myoclonus in pathologically proven progressive supranuclear palsy.

Kemp S, Harding AJ, Halliday GM, Mahant N, Fung VS. Kemp S, et al. Mov Disord. 2013 Nov;28(13):1804-6. doi: 10.1002/mds.25693. Epub 2013 Oct 4. Mov Disord. 2013. PMID: 24123159 No abstract available.

6

Unusual α-synuclein and cerebellar pathologies in a case of hereditary myoclonus-dystonia without SGCE mutation.

McCann H, Fung VS, Klein C, Halliday GM. McCann H, et al. Neuropathol Appl Neurobiol. 2015 Oct;41(6):837-42. doi: 10.1111/nan.12216. Epub 2015 May 2. Neuropathol Appl Neurobiol. 2015. PMID: 25582306 No abstract available.

7

Variants in the SNCA gene associate with motor progression while variants in the MAPT gene associate with the severity of Parkinson's disease.

Wang G, Huang Y, Chen W, Chen S, Wang Y, Xiao Q, Liu J, Fung VS, Halliday G, Chen S. Wang G, et al. Parkinsonism Relat Disord. 2016 Mar;24:89-94. doi: 10.1016/j.parkreldis.2015.12.018. Epub 2015 Dec 30. Parkinsonism Relat Disord. 2016. PMID: 26776090

8

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: fung vsc. 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.

9

Clinical and neuroimaging phenotypes of genetic parkinsonism from infancy to adolescence.

Morales-Briceño H, Mohammad SS, Post B, Fois AF, Dale RC, Tchan M, Fung VSC. Morales-Briceño H, et al. Brain. 2020 Mar 1;143(3):751-770. doi: 10.1093/brain/awz345. Brain. 2020. PMID: 31800013 Review.

10

The Head Retraction Reflex in Niemann-Pick Type C: A Novel Diagnostic Clue.

Martin AJ, Morales-Briceño H, Tchan M, Fung VSC. Martin AJ, et al. Mov Disord Clin Pract. 2020 Jun 18;7(5):543-547. doi: 10.1002/mdc3.12976. eCollection 2020 Jul. Mov Disord Clin Pract. 2020. PMID: 32626799 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

456 results

Search Page