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Results: 1-17 |
Results: 17
Lewy bodies and parkinsonism in families with parkin mutations
Authors: Farrer, M Chan, P Chen, R Tan, L Lincoln, S Hernandez, D Forno, L Gwinn-Hardy, K Petrucelli, L Hussey, J Singleton, A Tanner, C Hardy, J Langston, JW
Citation: M. Farrer et al., Lewy bodies and parkinsonism in families with parkin mutations, ANN NEUROL, 50(3), 2001, pp. 293-300
A clinical and pathological study of motor neurone disease on Guam
Authors: Morris, HR Al-Sarraj, S Schwab, C Gwinn-Hardy, K Perez-Tur, J Wood, NW Hardy, J Lees, AJ McGeer, PL Daniel, SE Steele, JC
Citation: Hr. Morris et al., A clinical and pathological study of motor neurone disease on Guam, BRAIN, 124, 2001, pp. 2215-2222
Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family
Authors: Gwinn-Hardy, K Singleton, A O'Suilleabhain, P Boss, M Nicholl, D Adam, A Hussey, J Critchley, P Hardy, J Farrer, M
Citation: K. Gwinn-hardy et al., Spinocerebellar ataxia type 3 phenotypically resembling Parkinson disease in a black family, ARCH NEUROL, 58(2), 2001, pp. 296-299
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
Authors: Lewis, J McGowan, E Rockwood, J Melrose, H Nacharaju, P Van Slegtenhorst, M Gwinn-Hardy, K Murphy, MP Baker, M Yu, X Duff, K Hardy, J Corral, A Lin, WL Yen, SH Dickson, DW Davies, P Hutton, M
Citation: J. Lewis et al., Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein, NAT GENET, 25(4), 2000, pp. 402-405
Amantadine is beneficial in restless legs syndrome
Authors: Evidente, VGH Adler, CH Caviness, JN Hentz, JG Gwinn-Hardy, K
Citation: Vgh. Evidente et al., Amantadine is beneficial in restless legs syndrome, MOVEMENT D, 15(2), 2000, pp. 324-327
Electrophysical observations in hereditary parkinsonism-dementia with Lewybody pathology
Authors: Caviness, JN Gwinn-Hardy, K Adler, CH Muenter, MD
Citation: Jn. Caviness et al., Electrophysical observations in hereditary parkinsonism-dementia with Lewybody pathology, MOVEMENT D, 15(1), 2000, pp. 140-145
Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese
Authors: Gwinn-Hardy, K Chen, JY Liu, HC Liu, TY Boss, M Seltzer, W Adam, A Singleton, A Koroshetz, W Waters, C Hardy, J Farrer, M
Citation: K. Gwinn-hardy et al., Spinocerebellar ataxia type 2 with parkinsonism in ethnic Chinese, NEUROLOGY, 55(6), 2000, pp. 800-805
Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p
Authors: Gwinn-Hardy, K Mehta, ND Farrer, M Maraganore, D Muenter, M Yen, SH Hardy, J Dickson, DW
Citation: K. Gwinn-hardy et al., Distinctive neuropathology revealed by alpha-synuclein antibodies in hereditary parkinsonism and dementia linked to chromosome 4p, ACT NEUROP, 99(6), 2000, pp. 663-672
Neurodegenerative disease: a different view of diagnosis
Authors: Hardy, J Gwinn-Hardy, K
Citation: J. Hardy et K. Gwinn-hardy, Neurodegenerative disease: a different view of diagnosis, MOL MED TOD, 5(12), 1999, pp. 514-517
The genetics of disorders with synuclein pathology and parkinsonism
Authors: Farrer, M Gwinn-Hardy, K Hutton, M Hardy, J
Citation: M. Farrer et al., The genetics of disorders with synuclein pathology and parkinsonism, HUM MOL GEN, 8(10), 1999, pp. 1901-1905
A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor
Authors: Farrer, M Gwinn-Hardy, K Muenter, M DeVrieze, FW Crook, R Perez-Tur, J Lincoln, S Maraganore, D Adler, C Newman, S MacElwee, K McCarthy, P Miller, C Waters, C Hardy, J
Citation: M. Farrer et al., A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor, HUM MOL GEN, 8(1), 1999, pp. 81-85
Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinson's disease
Authors: Lincoln, S Vaughan, J Wood, N Baker, M Adamson, J Gwinn-Hardy, K Lynch, T Hardy, J Farrer, M
Citation: S. Lincoln et al., Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinson's disease, NEUROREPORT, 10(2), 1999, pp. 427-429
Risperidone is effective in severe hemichorea/hemiballismus
Authors: Evidente, VGH Gwinn-Hardy, K Caviness, JN Adler, CH
Citation: Vgh. Evidente et al., Risperidone is effective in severe hemichorea/hemiballismus, MOVEMENT D, 14(2), 1999, pp. 377-379
A pilot study on the motor effects of rimantadine in Parkinson's disease
Authors: Evidente, VGH Adler, CH Caviness, JN Gwinn-Hardy, K
Citation: Vgh. Evidente et al., A pilot study on the motor effects of rimantadine in Parkinson's disease, CLIN NEUROP, 22(1), 1999, pp. 30-32
No pathogenic mutations in the beta-synuclein gene in Parkinson's disease
Authors: Lincoln, S Crook, R Chartier-Harlin, MC Gwinn-Hardy, K Baker, M Mouroux, V Richard, F Becquet, E Amouyel, P Destee, A Hardy, J Farrer, M
Citation: S. Lincoln et al., No pathogenic mutations in the beta-synuclein gene in Parkinson's disease, NEUROSCI L, 269(2), 1999, pp. 107-109
No pathogenic mutations in the persyn gene in Parkinson's disease
Authors: Lincoln, S Gwinn-Hardy, K Goudreau, J Chartier-Harlin, MC Baker, M Mouroux, V Richard, F Destee, A Becquet, E Amouyel, P Lynch, T Hardy, J Farrer, M
Citation: S. Lincoln et al., No pathogenic mutations in the persyn gene in Parkinson's disease, NEUROSCI L, 259(1), 1999, pp. 65-66
L-dopa slows the progression of familial parkinsonism
Authors: Gwinn-Hardy, K Evidente, VGH Waters, C Muenter, MD Hardy, J
Citation: K. Gwinn-hardy et al., L-dopa slows the progression of familial parkinsonism, LANCET, 353(9167), 1999, pp. 1850-1851
Risultati: 1-17 |