Ozelius LJ - Search Results

1

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.

2

Dinucleotide repeat polymorphism for the hexabrachion gene (HXB) on chromosome 9q32-34.

Ozelius L, Schuback DE, Stefansson K, Slaugenhaupt S, Gusella JF, Breakefield XO. Ozelius L, et al. Hum Mol Genet. 1992 May;1(2):141. doi: 10.1093/hmg/1.2.141-a. Hum Mol Genet. 1992. PMID: 1284469 No abstract available.

3

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.

4

A syndrome of autosomal dominant alternating hemiplegia: clinical presentation mimicking intractable epilepsy; chromosomal studies; and physiologic investigations.

Mikati MA, Maguire H, Barlow CF, Ozelius L, Breakefield XO, Klauck SM, Korf B, O'Tuama SL, Dangond F. Mikati MA, et al. Neurology. 1992 Dec;42(12):2251-7. doi: 10.1212/wnl.42.12.2251. Neurology. 1992. PMID: 1361034

5

A genetic linkage map of human chromosome 9q.

Ozelius LJ, Kwiatkowski DJ, Schuback DE, Breakefield XO, Wexler NS, Gusella JF, Haines JL. Ozelius LJ, et al. Genomics. 1992 Nov;14(3):715-20. doi: 10.1016/s0888-7543(05)80173-9. Genomics. 1992. PMID: 1427899 Free article.

6

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

7

BanI RFLP at AK1 locus (9q34).

Schuback DE, Ozelius L, Breakefield XO. Schuback DE, et al. Nucleic Acids Res. 1991 Oct 25;19(20):5798. doi: 10.1093/nar/19.20.5798-a. Nucleic Acids Res. 1991. PMID: 1682884 Free PMC article. No abstract available.

8

Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene.

Konradi C, Ozelius L, Breakefield XO. Konradi C, et al. Genomics. 1992 Jan;12(1):176-7. doi: 10.1016/0888-7543(92)90426-s. Genomics. 1992. PMID: 1733859 No abstract available.

9

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.

10

Dinucleotide repeat polymorphism (D16S285) on human chromosome 16.

Konradi C, Ozelius L, Yan W, Gusella JF, Breakefield XO. Konradi C, et al. Nucleic Acids Res. 1991 Oct 11;19(19):5449. doi: 10.1093/nar/19.19.5449. Nucleic Acids Res. 1991. PMID: 1923837 Free PMC article. No abstract available.

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