Ozelius LJ - Search Results

1

The role of mitochondrial DNA in Huntington's disease.

Irwin CC, Wexler NS, Young AB, Ozelius LJ, Penney JB, Shoulson I, Snodgrass SR, Ramos-Arroyo MA, Sanchez-Ramos J, Penchaszadeh GK, et al. Irwin CC, et al. Among authors: ozelius lj. J Mol Neurosci. 1989;1(2):129-36. doi: 10.1007/BF02896896. J Mol Neurosci. 1989. PMID: 2534902

2

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.

3

Partial linkage map of chromosome 13q in the region of the Wilson disease and retinoblastoma genes.

Haines JL, Ozelius L, St George-Hyslop P, Wexler NS, Gusella JF, Conneally PM. Haines JL, et al. Genet Epidemiol. 1988;5(6):375-80. doi: 10.1002/gepi.1370050602. Genet Epidemiol. 1988. PMID: 2905314

4

Expression of the early-onset torsion dystonia gene (DYT1) in human brain.

Augood SJ, Penney JB Jr, Friberg IK, Breakefield XO, Young AB, Ozelius LJ, Standaert DG. Augood SJ, et al. Among authors: ozelius lj. Ann Neurol. 1998 May;43(5):669-73. doi: 10.1002/ana.410430518. Ann Neurol. 1998. PMID: 9585364

5

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.

6

Distribution of the mRNAs encoding torsinA and torsinB in the normal adult human brain.

Augood SJ, Martin DM, Ozelius LJ, Breakefield XO, Penney JB Jr, Standaert DG. Augood SJ, et al. Among authors: ozelius lj. Ann Neurol. 1999 Nov;46(5):761-9. Ann Neurol. 1999. PMID: 10553994

7

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. Among authors: ozelius lj. Neurogenetics. 2001 Jul;3(3):133-43. doi: 10.1007/s100480100111. Neurogenetics. 2001. PMID: 11523564

8

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

9

Monoamine oxidase deficiency in males with an X chromosome deletion.

Sims KB, de la Chapelle A, Norio R, Sankila EM, Hsu YP, Rinehart WB, Corey TJ, Ozelius L, Powell JF, Bruns G, et al. Sims KB, et al. Neuron. 1989 Jan;2(1):1069-76. doi: 10.1016/0896-6273(89)90231-6. Neuron. 1989. PMID: 2483108

10

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

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