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Genetic risk variants in New Yorkers of Puerto Rican and Dominican Republic heritage with Parkinson's disease.
Miltenberger-Miltenyi G, Ortega RA, Domingo A, Yadav R, Nishiyama A, Raymond D, Katsnelson V, Urval N, Swan M, Shanker V, Miravite J, Walker RH, Bressman SB, Ozelius LJ, Cabassa JC, Saunders-Pullman R. Miltenberger-Miltenyi G, et al. Among authors: ozelius lj. NPJ Parkinsons Dis. 2023 Dec 7;9(1):160. doi: 10.1038/s41531-023-00599-6. NPJ Parkinsons Dis. 2023. PMID: 38062033 Free PMC article.
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
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
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.
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.
247 results