Multiple sclerosis

Citations 1-8 of 8 total displayed.

Original articles
Minocycline promotes dendritic spine maturation and improves behavioural performance in the fragile X mouse model

T V Bilousova, L Dansie, M Ngo, J Aye, J R Charles, D W Ethell, I M Ethell
J. Med. Genet. 2009 46: 94 -102; published online before print as 10.1136/jmg.2008.061796 [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendices ]  

Original articles
Interferon regulatory factor 5 (IRF5) gene variants are associated with multiple sclerosis in three distinct populations

G Kristjansdottir, J K Sandling, A Bonetti, I M Roos, L Milani, C Wang, S M Gustafsdottir, S Sigurdsson, A Lundmark, P J Tienari, K Koivisto, I Elovaara, T Pirttilä, M Reunanen, L Peltonen, J Saarela, J Hillert, T Olsson, U Landegren, A Alcina, O Fernández, L Leyva, M Guerrero, M Lucas, G Izquierdo, F Matesanz, A-C Syvänen
J. Med. Genet. 2008 45: 362 -369; published online before print as 10.1136/jmg.2007.055012 [Abstract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms

N Muncke, B S Wogatzky, M Breuning, E A Sistermans, V Endris, M Ross, D Vetrie, C E Catsman-Berrevoets, G Rappold
J. Med. Genet. 2004; 41: e121. [Extract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
A novel neurodegenerative disease characterised by posterior column ataxia and pyramidal tract involvement maps to chromosome 8p12–8q12.1

P N Valdmanis, A A Simões Lopes, F Gros-Louis, J D Stewart, G A Rouleau, N Dupré
J. Med. Genet. 2004; 41: 634-639. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Early onset, non-progressive, mild cerebellar ataxia co-segregating with a familial balanced translocation t(8;20)(p22;q13)

J M Hertz, B Sivertsen, A Silahtaroglu, M Bugge, V Kalscheuer, A Weber, J Wirth, H-H Ropers, N Tommerup, Z Tümer
J. Med. Genet. 2004; 41: e25. [Extract] [Full text] [PDF] [Request Permissions]  

Review articles
New approaches to investigating heterogeneity in complex traits

R Bomprezzi, P E Kovanen, R Martin
J. Med. Genet. 2003; 40: 553-559. [Abstract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Two novel aspartoacylase gene (ASPA) missense mutations specific to Norwegian and Swedish patients with Canavan disease

T R Olsen, L Tranebjærg, E A Kvittingen, L Hagenfeldt, C Møller, Ø Nilssen
J. Med. Genet. 2002; 39: e55. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
A partial deletion of the aspartoacylase gene is the cause of Canavan disease in a family from Mexico

FATMA ELA TAHMAZ, SIMA SAM, GEORGE E HOGANSON, FRANKLIN QUAN
J. Med. Genet. 2001; 38: e9. [Extract] [Full text] [PDF] [Request Permissions]