Ozelius LJ - Search Results

1

DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease.

Hedrich K, Djarmati A, Schäfer N, Hering R, Wellenbrock C, Weiss PH, Hilker R, Vieregge P, Ozelius LJ, Heutink P, Bonifati V, Schwinger E, Lang AE, Noth J, Bressman SB, Pramstaller PP, Riess O, Klein C. Hedrich K, et al. Among authors: ozelius lj. Neurology. 2004 Feb 10;62(3):389-94. doi: 10.1212/01.wnl.0000113022.51739.88. Neurology. 2004. PMID: 14872018

2

Dystonia gene in Ashkenazi Jewish population is located on chromosome 9q32-34.

Kramer PL, de Leon D, Ozelius L, Risch N, Bressman SB, Brin MF, Schuback DE, Burke RE, Kwiatkowski DJ, Shale H, et al. Kramer PL, et al. Ann Neurol. 1990 Feb;27(2):114-20. doi: 10.1002/ana.410270203. Ann Neurol. 1990. PMID: 2317008

3

Dystonia in Ashkenazi Jews: clinical characterization of a founder mutation.

Bressman SB, de Leon D, Kramer PL, Ozelius LJ, Brin MF, Greene PE, Fahn S, Breakefield XO, Risch NJ. Bressman SB, et al. Among authors: ozelius lj. Ann Neurol. 1994 Nov;36(5):771-7. doi: 10.1002/ana.410360514. Ann Neurol. 1994. PMID: 7979224

4

A study of idiopathic torsion dystonia in a non-Jewish family: evidence for genetic heterogeneity.

Bressman SB, Heiman GA, Nygaard TG, Ozelius LJ, Hunt AL, Brin MF, Gordon MF, Moskowitz CB, de Leon D, Burke RE, et al. Bressman SB, et al. Among authors: ozelius lj. Neurology. 1994 Feb;44(2):283-7. doi: 10.1212/wnl.44.2.283. Neurology. 1994. PMID: 8309575

5

Secondary dystonia and the DYTI gene.

Bressman SB, de Leon D, Raymond D, Greene PE, Brin MF, Fahn S, Ozelius LJ, Breakefield XO, Kramer PL, Risch NJ. Bressman SB, et al. Among authors: ozelius lj. Neurology. 1997 Jun;48(6):1571-7. doi: 10.1212/wnl.48.6.1571. Neurology. 1997. PMID: 9191768

6

De novo mutations (GAG deletion) in the DYT1 gene in two non-Jewish patients with early-onset dystonia.

Klein C, Brin MF, de Leon D, Limborska SA, Ivanova-Smolenskaya IA, Bressman SB, Friedman A, Markova ED, Risch NJ, Breakefield XO, Ozelius LJ. Klein C, et al. Among authors: ozelius lj. Hum Mol Genet. 1998 Jul;7(7):1133-6. doi: 10.1093/hmg/7.7.1133. Hum Mol Genet. 1998. PMID: 9618171

7

Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South Tyrol.

Klein C, Pramstaller PP, Castellan CC, Breakefield XO, Kramer PL, Ozelius LJ. Klein C, et al. Among authors: ozelius lj. Ann Neurol. 1998 Sep;44(3):394-8. doi: 10.1002/ana.410440318. Ann Neurol. 1998. PMID: 9749609

8

Clinical-genetic spectrum of primary dystonia.

Bressman SB, de Leon D, Raymond D, Ozelius LJ, Breakefield XO, Nygaard TG, Almasy L, Risch NJ, Kramer PL. Bressman SB, et al. Among authors: ozelius lj. Adv Neurol. 1998;78:79-91. Adv Neurol. 1998. PMID: 9750905 Review. No abstract available.

9

The gene (DYT1) for early-onset torsion dystonia encodes a novel protein related to the Clp protease/heat shock family.

Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Jacoby D, Penney J, Risch NJ, Fahn S, Gusella JF, Breakefield XO. Ozelius LJ, et al. Adv Neurol. 1998;78:93-105. Adv Neurol. 1998. PMID: 9750906 Review. No abstract available.

10

The role of the DYT1 gene in secondary dystonia.

Bressman SB, de Leon D, Raymond D, Greene PE, Brin MF, Fahn S, Ozelius LJ, Breakefield XO, Kramer PL, Risch NJ. Bressman SB, et al. Among authors: ozelius lj. Adv Neurol. 1998;78:107-15. Adv Neurol. 1998. PMID: 9750907 No abstract available.

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