Functional genetic analysis of motor neuron disease by Bäumer, D

TARDBP in amyotrophic lateral sclerosis: identification of a novel variant but absence of copy number variation. by Bäumer, D, Parkinson, N, Talbot, K

Advances in motor neurone disease. by Bäumer, D, Talbot, K, Turner, M

The role of RNA processing in the pathogenesis of motor neuron degeneration. by Bäumer, D, Ansorge, O, Almeida, M, Talbot, K

The role of RNA processing in the pathogenesis of motor neuron degeneration by Bäumer, D, Ansorge, O, Almeida, M, Talbot, K

Pre-symptomatic development of lower motor neuron connectivity in a mouse model of severe spinal muscular atrophy. by Murray, L, Lee, S, Bäumer, D, Parson, S, Talbot, K, Gillingwater, T

Candidate screening of the bovine and feline spinal muscular atrophy genes reveals no evidence for involvement in human motor neuron disorders. by Parkinson, N, Baumer, D, Rose-Morris, A, Talbot, K

CIDP presenting as recurrent severe back pain without weakness or sensory loss. by Bäumer, D, Grant, D, Knight, R, Buckley, C, Bennett, D, Rinaldi, S

Primary angiitis of the CNS mimicking a spinal cord tumour. by Baumer, D, Flossmann, E, Cudlip, S, Quaghebeur, G, Jeans, A, Talbot, K

Progressive hemiparesis (Mills syndrome) with aphasia in amyotrophic lateral sclerosis. by Bäumer, D, Butterworth, R, Menke, R, Talbot, K, Hofer, M, Turner, M

TDP-43 expression in mouse models of amyotrophic lateral sclerosis and spinal muscular atrophy by Turner, B, Bäumer, D, Parkinson, N, Scaber, J, Ansorge, O, Talbot, K

FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion. by Bäumer, D, East, S, Tseu, B, Zeman, A, Hilton, D, Talbot, K, Ansorge, O

Juvenile ALS with basophilic inclusions is a FUS proteinopathy with FUS mutations. by Bäumer, D, Hilton, D, Paine, S, Turner, M, Lowe, J, Talbot, K, Ansorge, O

Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. by Bäumer, D, Lee, S, Nicholson, G, Davies, J, Parkinson, N, Murray, L, Gillingwater, T, Ansorge, O, Davies, K, Talbot, K

IgG1 pan-neurofascin antibodies identify a severe yet treatable neuropathy with a high mortality by Fehmi, J, Davies, AJ, Walters, J, Lavin, T, Keh, R, Rossor, AM, Munteanu, T, Delanty, N, Roberts, R, Bäumer, D, Lennox, G, Rinaldi, S