Leung JC - Search Results

1

TorsinA protein and neuropathology in early onset generalized dystonia with GAG deletion.

Rostasy K, Augood SJ, Hewett JW, Leung JC, Sasaki H, Ozelius LJ, Ramesh V, Standaert DG, Breakefield XO, Hedreen JC. Rostasy K, et al. Among authors: leung jc. Neurobiol Dis. 2003 Feb;12(1):11-24. doi: 10.1016/s0969-9961(02)00010-4. Neurobiol Dis. 2003. PMID: 12609485

2

Molecular cloning and expression of rat torsinA in the normal and genetically dystonic (dt) rat.

Ziefer P, Leung J, Razzano T, Shalish C, LeDoux MS, Lorden JF, Ozelius L, Breakefield XO, Standaert DG, Augood SJ. Ziefer P, et al. Brain Res Mol Brain Res. 2002 May 30;101(1-2):132-5. doi: 10.1016/s0169-328x(02)00176-6. Brain Res Mol Brain Res. 2002. PMID: 12007841

3

Novel mutation in the TOR1A (DYT1) gene in atypical early onset dystonia and polymorphisms in dystonia and early onset parkinsonism.

Leung JC, Klein C, Friedman J, Vieregge P, Jacobs H, Doheny D, Kamm C, DeLeon D, Pramstaller PP, Penney JB, Eisengart M, Jankovic J, Gasser T, Bressman SB, Corey DP, Kramer P, Brin MF, Ozelius LJ, Breakefield XO. Leung JC, et al. Neurogenetics. 2001 Jul;3(3):133-43. doi: 10.1007/s100480100111. Neurogenetics. 2001. PMID: 11523564

4

The TOR1A (DYT1) gene family and its role in early onset torsion dystonia.

Ozelius LJ, Page CE, Klein C, Hewett JW, Mineta M, Leung J, Shalish C, Bressman SB, de Leon D, Brin MF, Fahn S, Corey DP, Breakefield XO. Ozelius LJ, et al. Genomics. 1999 Dec 15;62(3):377-84. doi: 10.1006/geno.1999.6039. Genomics. 1999. PMID: 10644435

5

The GAG deletion of the DYT1 gene is infrequent in musicians with focal dystonia.

Friedman JR, Klein C, Leung J, Woodward H, Ozelius LJ, Breakefield XO, Charness ME. Friedman JR, et al. Neurology. 2000 Nov 14;55(9):1417-8. doi: 10.1212/wnl.55.9.1417. Neurology. 2000. PMID: 11087801 No abstract available.

6

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

7

Epsilon-sarcoglycan mutations found in combination with other dystonia gene mutations.

Klein C, Liu L, Doheny D, Kock N, Müller B, de Carvalho Aguiar P, Leung J, de Leon D, Bressman SB, Silverman J, Smith C, Danisi F, Morrison C, Walker RH, Velickovic M, Schwinger E, Kramer PL, Breakefield XO, Brin MF, Ozelius LJ. Klein C, et al. Ann Neurol. 2002 Nov;52(5):675-9. doi: 10.1002/ana.10358. Ann Neurol. 2002. PMID: 12402271

8

Clinical findings of a myoclonus-dystonia family with two distinct mutations.

Doheny D, Danisi F, Smith C, Morrison C, Velickovic M, De Leon D, Bressman SB, Leung J, Ozelius L, Klein C, Breakefield XO, Brin MF, Silverman JM. Doheny D, et al. Neurology. 2002 Oct 22;59(8):1244-6. doi: 10.1212/wnl.59.8.1244. Neurology. 2002. PMID: 12391355

9

Dopamine transmission in DYT1 dystonia.

Augood SJ, Hollingsworth Z, Albers DS, Yang L, Leung J, Breakefield XO, Standaert DG. Augood SJ, et al. Adv Neurol. 2004;94:53-60. Adv Neurol. 2004. PMID: 14509654 No abstract available.

10

Refined linkage to the RDP/DYT12 locus on 19q13.2 and evaluation of GRIK5 as a candidate gene.

Kamm C, Leung J, Joseph S, Dobyns WB, Brashear A, Breakefield XO, Ozelius LJ. Kamm C, et al. Mov Disord. 2004 Jul;19(7):845-847. doi: 10.1002/mds.20095. Mov Disord. 2004. PMID: 15254951

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