AAAAAA

   
Results: 1-7 |
Results: 7
A conserved sorting-associated protein is mutant in chorea-acanthocytosis
Authors: Rampoldi, L Dobson-Stone, C Rubio, JP Danek, A Chalmers, RM Wood, NW Verellen, C Ferrer, X Malandrini, A Fabrizi, GM Brown, R Vance, J Pericak-Vance, M Rudolf, G Carre, S Alonso, E Manfredi, M Nemeth, AH Monaco, AP
Citation: L. Rampoldi et al., A conserved sorting-associated protein is mutant in chorea-acanthocytosis, NAT GENET, 28(2), 2001, pp. 119-120
A prevalence study of primary dystonia in eight European countries
Authors: Warner, T Camfield, L Marsden, CD Nemeth, AH Hyman, N Harley, D Wissel, J Poewe, W Marttila, RJ Erjanti, H Burbaud, P Lagueny, A Kamm, C Gasser, T Franz, D Castelon-Konkiewitz, E Trender, I Ceballos-Baumann, A Nebe, A Freudenberg, B Bentivoglio, A Cassetta, E Albanese, A Curra, A Vacca, L Berardelli, A Ferreira, J Sampaio, C Passao, V Marti, F Tolosa, E Claveria, L Duarte, J Ben-Shlomo, Y Newton, A
Citation: T. Warner et al., A prevalence study of primary dystonia in eight European countries, J NEUROL, 247(10), 2000, pp. 787-792
Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34
Authors: Nemeth, AH Bochukova, E Dunne, E Huson, SM Elston, J Hannan, MA Jackson, M Chapman, CJ Taylor, AMR
Citation: Ah. Nemeth et al., Autosomal recessive cerebellar ataxia with oculomotor apraxia (ataxia-telangiectasia-like syndrome) is linked to chromosome 9q34, AM J HU GEN, 67(5), 2000, pp. 1320-1326
Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3)
Authors: Nemeth, AH Nolte, D Dunne, E Niemann, S Kostrzewa, M Peters, U Fraser, E Bochukova, E Butler, R Brown, J Cox, RD Levy, ER Ropers, HH Monaco, AP Muller, U
Citation: Ah. Nemeth et al., Refined linkage disequilibrium and physical mapping of the gene locus for X-linked dystonia-parkinsonism (DYT3), GENOMICS, 60(3), 1999, pp. 320-329
Do the same genes predispose to Gilles de la Tourette Syndrome and dystonia? Report of a new family and review of the literature
Authors: Nemeth, AH Mills, KR Elston, JS Williams, A Dunne, E Hyman, NM
Citation: Ah. Nemeth et al., Do the same genes predispose to Gilles de la Tourette Syndrome and dystonia? Report of a new family and review of the literature, MOVEMENT D, 14(5), 1999, pp. 826-831
A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degeneration
Authors: Dunne, E Hyman, NM Huson, SM Nemeth, AH
Citation: E. Dunne et al., A novel point mutation in X-linked adrenoleukodystrophy presenting as a spinocerebellar degeneration, ANN NEUROL, 45(5), 1999, pp. 652-655
Sex-related influences on the frequency and age of onset of primary dystonia
Authors: Warner, T Camfield, L Marsden, CD Wissel, J Poewe, W Marttila, RJ Erjanti, H Burbaud, P Lagueny, A Kamm, C Gasser, T Franz, P Castelon-Konkiewitz, E Trender, I Ceballos-Baumann, A Nebe, A Freudenberg, B Bentivoglio, A Cassetta, E Albanese, A Curra, A Vacca, L Berardelli, A Ferreira, J Sampaio, C Passao, V Marti, F Tolosa, E Claveria, L Duarte, J Nemeth, AH Hyman, N Harley, D Warner, T Ben-Shlomo, Y Newton, A
Citation: T. Warner et al., Sex-related influences on the frequency and age of onset of primary dystonia, NEUROLOGY, 53(8), 1999, pp. 1871-1873
Risultati: 1-7 |