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678 results

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Page 1
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.
Exclusion of the DYT1 locus in familial torticollis.
Bressman SB, Warner TT, Almasy L, Uitti RJ, Greene PE, Heiman GA, Raymond D, Ford B, de Leon D, Fahn S, Kramer PL, Risch NJ, Maraganore DM, Nygaard TG, Harding AE. Bressman SB, et al. Among authors: raymond d. Ann Neurol. 1996 Oct;40(4):681-4. doi: 10.1002/ana.410400421. Ann Neurol. 1996. PMID: 8871591
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
The early-onset torsion dystonia gene (DYT1) encodes an ATP-binding protein.
Ozelius LJ, Hewett JW, Page CE, Bressman SB, Kramer PL, Shalish C, de Leon D, Brin MF, Raymond D, Corey DP, Fahn S, Risch NJ, Buckler AJ, Gusella JF, Breakefield XO. Ozelius LJ, et al. Among authors: raymond d. Nat Genet. 1997 Sep;17(1):40-8. doi: 10.1038/ng0997-40. Nat Genet. 1997. PMID: 9288096
Idiopathic torsion dystonia linked to chromosome 8 in two Mennonite families.
Almasy L, Bressman SB, Raymond D, Kramer PL, Greene PE, Heiman GA, Ford B, Yount J, de Leon D, Chouinard S, Saunders-Pullman R, Brin MF, Kapoor RP, Jones AC, Shen H, Fahn S, Risch NJ, Nygaard TG. Almasy L, et al. Among authors: raymond d. Ann Neurol. 1997 Oct;42(4):670-3. doi: 10.1002/ana.410420421. Ann Neurol. 1997. PMID: 9382482
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.
Localization of a gene for myoclonus-dystonia to chromosome 7q21-q31.
Nygaard TG, Raymond D, Chen C, Nishino I, Greene PE, Jennings D, Heiman GA, Klein C, Saunders-Pullman RJ, Kramer P, Ozelius LJ, Bressman SB. Nygaard TG, et al. Among authors: raymond d. Ann Neurol. 1999 Nov;46(5):794-8. doi: 10.1002/1531-8249(199911)46:5<794::aid-ana19>3.0.co;2-2. Ann Neurol. 1999. PMID: 10554001
Evaluation of the role of the D2 dopamine receptor in myoclonus dystonia.
Klein C, Gurvich N, Sena-Esteves M, Bressman S, Brin MF, Ebersole BJ, Fink S, Forsgren L, Friedman J, Grimes D, Holmgren G, Kyllerman M, Lang AE, de Leon D, Leung J, Prioleau C, Raymond D, Sanner G, Saunders-Pullman R, Vieregge P, Wahlström J, Breakefield XO, Kramer PL, Ozelius LJ, Sealfon SC. Klein C, et al. Among authors: raymond d. Ann Neurol. 2000 Mar;47(3):369-73. Ann Neurol. 2000. PMID: 10716258
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
678 results