Ozelius LJ - Search Results

1

Phenotypic features of myoclonus-dystonia in three kindreds.

Doheny DO, Brin MF, Morrison CE, Smith CJ, Walker RH, Abbasi S, Müller B, Garrels J, Liu L, De Carvalho Aguiar P, Schilling K, Kramer P, De Leon D, Raymond D, Saunders-Pullman R, Klein C, Bressman SB, Schmand B, Tijssen MA, Ozelius LJ, Silverman JM. Doheny DO, et al. Among authors: ozelius lj. Neurology. 2002 Oct 22;59(8):1187-96. doi: 10.1212/wnl.59.8.1187. Neurology. 2002. PMID: 12391346

2

Strong allelic association between the torsion dystonia gene (DYT1) andloci on chromosome 9q34 in Ashkenazi Jews.

Ozelius LJ, Kramer PL, de Leon D, Risch N, Bressman SB, Schuback DE, Brin MF, Kwiatkowski DJ, Burke RE, Gusella JF, et al. Ozelius LJ, et al. Am J Hum Genet. 1992 Mar;50(3):619-28. Am J Hum Genet. 1992. PMID: 1347197 Free PMC article.

3

Dopamine beta-hydroxylase gene excluded in four subtypes of hereditary dystonia.

Schuback D, Kramer P, Ozelius L, Holmgren G, Forsgren L, Kyllerman M, Wahlström J, Craft CM, Nygaard T, Brin M, et al. Schuback D, et al. Hum Genet. 1991 Jul;87(3):311-6. doi: 10.1007/BF00200910. Hum Genet. 1991. PMID: 1677923

4

Torsion dystonia genes in two populations confined to a small region on chromosome 9q32-34.

Kwiatkowski DJ, Ozelius L, Kramer PL, Perman S, Schuback DE, Gusella JF, Fahn S, Breakefield XO. Kwiatkowski DJ, et al. Am J Hum Genet. 1991 Aug;49(2):366-71. Am J Hum Genet. 1991. PMID: 1867195 Free PMC article.

5

Identification of a highly polymorphic microsatellite VNTR within the argininosuccinate synthetase locus: exclusion of the dystonia gene on 9q32-34 as the cause of dopa-responsive dystonia in a large kindred.

Kwiatkowski DJ, Nygaard TG, Schuback DE, Perman S, Trugman JM, Bressman SB, Burke RE, Brin MF, Ozelius L, Breakefield XO, et al. Kwiatkowski DJ, et al. Am J Hum Genet. 1991 Jan;48(1):121-8. Am J Hum Genet. 1991. PMID: 1985454 Free PMC article.

6

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

7

Human gene for torsion dystonia located on chromosome 9q32-q34.

Ozelius L, Kramer PL, Moskowitz CB, Kwiatkowski DJ, Brin MF, Bressman SB, Schuback DE, Falk CT, Risch N, de Leon D, et al. Ozelius L, et al. Neuron. 1989 May;2(5):1427-34. doi: 10.1016/0896-6273(89)90188-8. Neuron. 1989. PMID: 2576373

8

Molecular genetics of an autosomal dominant form of torsion dystonia.

Kramer PL, Ozelius L, Brin MF, Fahn S, Kidd KK, Gusella J, Breakefield XO. Kramer PL, et al. Adv Neurol. 1988;50:57-66. Adv Neurol. 1988. PMID: 2899954 No abstract available.

9

Linkage analysis in a family with dominantly inherited torsion dystonia: exclusion of the pro-opiomelanocortin and glutamic acid decarboxylase genes and other chromosomal regions using DNA polymorphisms.

Breakefield XO, Bressman SB, Kramer PL, Ozelius L, Moskowitz C, Tanzi R, Brin MF, Hobbs W, Kaufman D, Tobin A, et al. Breakefield XO, et al. J Neurogenet. 1986 May;3(3):159-75. doi: 10.3109/01677068609106846. J Neurogenet. 1986. PMID: 3016220

10

Exclusion of autosomal dominant dystonia gene from large regions of chromosomes 11p, 13q, and 21q by multi-point linkage analysis.

Kramer PL, Ozelius L, Gusella JF, Fahn S, Kidd KK, Breakefield XO. Kramer PL, et al. Genet Epidemiol. 1987;4(5):377-86. doi: 10.1002/gepi.1370040506. Genet Epidemiol. 1987. PMID: 3692135

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