Raymond D - Search Results

1

International Genetic Testing and Counseling Practices for Parkinson's Disease.

Saunders-Pullman R, Raymond D, Ortega RA, Shalash A, Gatto E, Salari M, Markgraf M, Alcalay RN, Mascalzoni D, Mencacci NE, Bonifati V, Merello M, Chung SJ, Novakovic I, Bardien S, Pal G, Hall A, Hattori N, Lynch T, Thaler A, Sue CM, Foroud T, Verbrugge J, Schulze J, Cook L, Marder K, Suchowersky O, Klein C, Simuni T. Saunders-Pullman R, et al. Among authors: raymond d. Mov Disord. 2023 Aug;38(8):1527-1535. doi: 10.1002/mds.29442. Epub 2023 Jun 13. Mov Disord. 2023. PMID: 37310233

2

Myoclonus dystonia: possible association with obsessive-compulsive disorder and alcohol dependence.

Saunders-Pullman R, Shriberg J, Heiman G, Raymond D, Wendt K, Kramer P, Schilling K, Kurlan R, Klein C, Ozelius LJ, Risch NJ, Bressman SB. Saunders-Pullman R, et al. Among authors: raymond d. Neurology. 2002 Jan 22;58(2):242-5. doi: 10.1212/wnl.58.2.242. Neurology. 2002. PMID: 11805251

3

Age at onset as a factor in determining the phenotype of primary torsion dystonia.

O'Riordan S, Raymond D, Lynch T, Saunders-Pullman R, Bressman SB, Daly L, Hutchinson M. O'Riordan S, et al. Among authors: raymond d. Neurology. 2004 Oct 26;63(8):1423-6. doi: 10.1212/01.wnl.0000142035.26034.c2. Neurology. 2004. PMID: 15505159

4

High mutation rate in dopa-responsive dystonia: detection with comprehensive GCHI screening.

Hagenah J, Saunders-Pullman R, Hedrich K, Kabakci K, Habermann K, Wiegers K, Mohrmann K, Lohnau T, Raymond D, Vieregge P, Nygaard T, Ozelius LJ, Bressman SB, Klein C. Hagenah J, et al. Among authors: raymond d. Neurology. 2005 Mar 8;64(5):908-11. doi: 10.1212/01.WNL.0000152839.50258.A2. Neurology. 2005. PMID: 15753436

5

Phenotypic spectrum and sex effects in eleven myoclonus-dystonia families with epsilon-sarcoglycan mutations.

Raymond D, Saunders-Pullman R, de Carvalho Aguiar P, Schule B, Kock N, Friedman J, Harris J, Ford B, Frucht S, Heiman GA, Jennings D, Doheny D, Brin MF, de Leon Brin D, Multhaupt-Buell T, Lang AE, Kurlan R, Klein C, Ozelius L, Bressman S. Raymond D, et al. Mov Disord. 2008 Mar 15;23(4):588-92. doi: 10.1002/mds.21785. Mov Disord. 2008. PMID: 18175340

6

Responsiveness to levodopa in epsilon-sarcoglycan deletions.

Luciano MS, Ozelius L, Sims K, Raymond D, Liu L, Saunders-Pullman R. Luciano MS, et al. Among authors: raymond d. Mov Disord. 2009 Feb 15;24(3):425-8. doi: 10.1002/mds.22375. Mov Disord. 2009. PMID: 19133653

7

Mutations in the THAP1 gene are responsible for DYT6 primary torsion dystonia.

Fuchs T, Gavarini S, Saunders-Pullman R, Raymond D, Ehrlich ME, Bressman SB, Ozelius LJ. Fuchs T, et al. Among authors: raymond d. Nat Genet. 2009 Mar;41(3):286-8. doi: 10.1038/ng.304. Epub 2009 Feb 1. Nat Genet. 2009. PMID: 19182804

8

Mutations in THAP1 (DYT6) in early-onset dystonia: a genetic screening study.

Bressman SB, Raymond D, Fuchs T, Heiman GA, Ozelius LJ, Saunders-Pullman R. Bressman SB, et al. Among authors: raymond d. Lancet Neurol. 2009 May;8(5):441-6. doi: 10.1016/S1474-4422(09)70081-X. Epub 2009 Apr 1. Lancet Neurol. 2009. PMID: 19345147 Free PMC article.

9

Genetic evidence for an association of the TOR1A locus with segmental/focal dystonia.

Sharma N, Franco RA Jr, Kuster JK, Mitchell AA, Fuchs T, Saunders-Pullman R, Raymond D, Brin MF, Blitzer A, Bressman SB, Ozelius LJ. Sharma N, et al. Among authors: raymond d. Mov Disord. 2010 Oct 15;25(13):2183-7. doi: 10.1002/mds.23225. Mov Disord. 2010. PMID: 20669276 Free PMC article.

10

LRRK2 G2019S mutations are associated with an increased cancer risk in Parkinson disease.

Saunders-Pullman R, Barrett MJ, Stanley KM, Luciano MS, Shanker V, Severt L, Hunt A, Raymond D, Ozelius LJ, Bressman SB. Saunders-Pullman R, et al. Among authors: raymond d. Mov Disord. 2010 Nov 15;25(15):2536-41. doi: 10.1002/mds.23314. Mov Disord. 2010. PMID: 20818610 Free PMC article.

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