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Arm swing as a potential new prodromal marker of Parkinson's disease.
Mirelman A, Bernad-Elazari H, Thaler A, Giladi-Yacobi E, Gurevich T, Gana-Weisz M, Saunders-Pullman R, Raymond D, Doan N, Bressman SB, Marder KS, Alcalay RN, Rao AK, Berg D, Brockmann K, Aasly J, Waro BJ, Tolosa E, Vilas D, Pont-Sunyer C, Orr-Urtreger A, Hausdorff JM, Giladi N. Mirelman A, et al. Among authors: raymond d. Mov Disord. 2016 Oct;31(10):1527-1534. doi: 10.1002/mds.26720. Mov Disord. 2016. PMID: 27430880 Free PMC article.
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: raymond d. 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: raymond d. 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: raymond d. Adv Neurol. 1998;78:107-15. Adv Neurol. 1998. PMID: 9750907 No abstract available.
The DYT1 phenotype and guidelines for diagnostic testing.
Bressman SB, Sabatti C, Raymond D, de Leon D, Klein C, Kramer PL, Brin MF, Fahn S, Breakefield X, Ozelius LJ, Risch NJ. Bressman SB, et al. Among authors: raymond d. Neurology. 2000 May 9;54(9):1746-52. doi: 10.1212/wnl.54.9.1746. Neurology. 2000. PMID: 10802779
Diagnostic criteria for dystonia in DYT1 families.
Bressman SB, Raymond D, Wendt K, Saunders-Pullman R, De Leon D, Fahn S, Ozelius L, Risch N. Bressman SB, et al. Among authors: raymond d. Neurology. 2002 Dec 10;59(11):1780-2. doi: 10.1212/01.wnl.0000035630.12515.e0. Neurology. 2002. PMID: 12473770 Clinical Trial.
Phenylalanine loading as a diagnostic test for DRD: interpreting the utility of the test.
Saunders-Pullman R, Blau N, Hyland K, Zschocke J, Nygaard T, Raymond D, Shanker V, Mohrmann K, Arnold L, Tabbal S, deLeon D, Ford B, Brin M, Chouinard S, Ozelius L, Klein C, Bressman SB. Saunders-Pullman R, et al. Among authors: raymond d. Mol Genet Metab. 2004 Nov;83(3):207-12. doi: 10.1016/j.ymgme.2004.07.010. Mol Genet Metab. 2004. PMID: 15542391
667 results