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Results: 1-10 |
Results: 10
A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2
Authors: Holmes, SE O'Hearn, E Rosenblatt, A Callahan, C Hwang, HS Ingersoll-Ashworth, RG Fleisher, A Stevanin, G Brice, A Potter, NT Ross, CA Margolis, RL
Citation: Se. Holmes et al., A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington disease-like 2, NAT GENET, 29(4), 2001, pp. 377-378
Prevalence, clinical manifestations, etiology, and treatment of depressionin Parkinson's disease
Authors: Slaughter, JR Slaughter, KA Nichols, D Holmes, SE Martens, RP
Citation: Jr. Slaughter et al., Prevalence, clinical manifestations, etiology, and treatment of depressionin Parkinson's disease, J NEUROP CL, 13(2), 2001, pp. 187-196
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion (vol 50, pg 373, 2001)
Authors: Margolis, RL O'Hearn, E Rosenblatt, A Willour, V Holmes, SE Franz, ML Callahan, C Hwang, HS Troncoso, JC Ross, CA
Citation: Rl. Margolis et al., A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion (vol 50, pg 373, 2001), ANN NEUROL, 50(6), 2001, pp. 830-380B
A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion
Authors: Margolis, RL O'Hearn, E Rosenblatt, A Willour, V Holmes, SE Franz, ML Callahan, C Hwang, HS Troncoso, JC Ross, CA
Citation: Rl. Margolis et al., A disorder similar to Huntington's disease is associated with a novel CAG repeat expansion, ANN NEUROL, 50(3), 2001, pp. 373-380
SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family
Authors: Fujigasaki, H Verma, IC Camuzat, A Margolis, RL Zander, C Lebre, AS Jamot, L Saxena, R Anand, I Holmes, SE Ross, CA Durr, A Brice, A
Citation: H. Fujigasaki et al., SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study ofan Indian family, ANN NEUROL, 49(1), 2001, pp. 117-121
SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia
Authors: Holmes, SE O'Hearn, E Ross, CA Margolis, RL
Citation: Se. Holmes et al., SCA12: An unusual mutation leads to an unusual spinocerebellar ataxia, BRAIN RES B, 56(3-4), 2001, pp. 397-403
SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion
Authors: O'Hearn, E Holmes, SE Calvert, PC Ross, CA Margolis, RL
Citation: E. O'Hearn et al., SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion, NEUROLOGY, 56(3), 2001, pp. 299-303
Risk factors in childhood that lead to the development of conduct disorderand antisocial personality disorder
Authors: Holmes, SE Slaughter, JR Kashani, J
Citation: Se. Holmes et al., Risk factors in childhood that lead to the development of conduct disorderand antisocial personality disorder, CHILD PSYCH, 31(3), 2001, pp. 183-193
Comparison of therapeutic factors in group and individual treatment processes
Authors: Holmes, SE Kivlighan, DM
Citation: Se. Holmes et Dm. Kivlighan, Comparison of therapeutic factors in group and individual treatment processes, J COUN PSYC, 47(4), 2000, pp. 478-484
Expansion of a novel CAG trinucleotide repeat in the 5 ' region of PPP2R2Bis associated with SCA12
Authors: Holmes, SE O'Hearn, EE McInnis, MG Gorelick-Feldman, DA Kleiderlein, JJ Callahan, C Kwak, NG Ingersoll-Ashworth, RG Sherr, M Sumner, AJ Sharp, AH Ananth, U Seltzer, WK Boss, MA Vieria-Saecker, AM Epplen, JT Riess, O Ross, CA Margolis, RL
Citation: Se. Holmes et al., Expansion of a novel CAG trinucleotide repeat in the 5 ' region of PPP2R2Bis associated with SCA12, NAT GENET, 23(4), 1999, pp. 391-392
Risultati: 1-10 |