James PA, Cader MZ, Muntoni F, Childs A-M, Crow YJ and Talbot K (2006)  Severe childhood SMA and axonal CMT due to anti-codon binding domain mutations in the GARS gene  Neurology 67(9):1710-2

Talbot K and Ansorge O (2006)  Recent advances in the genetics of  Amyotrophic Lateral Sclerosis and Fronto-temporal Dementia: common pathways in neurodegenerative disease Hum Mol Genet 15 Spec No 2:R182-7

James P and Talbot K (2006)  Non-ALS forms of inherited motor neuron degeneration.  In Molecular Basis of Amyotrophic Lateral Sclerosis:  Biochim Biophys Acta  May 5 [Epub ahead of print], 1762(11-12):986-1000

Ackerley S, James P, Kalli A, French S, Davies KE and Talbot K (2006)  Mutation in the small heat shock protein hspB1 leading to distal hereditary motor neuronopathy disrupts neurofilament assembly and the axonal transport of specific cellular cargoes  Hum Mol Genet 15(2):347-54

Evgrafov OV, Mersiyanova I, Irobi J, Van Den Bosch L, Dierick I, Leung CL, Schagina O, Verpoorten N, Van Impe K, Fedotov V, Dadali E, Auer-Grumbach M, Windpassinger C, Wagner K, Mitrovic Z, Hilton-Jones D, Talbot K, Martin JJ, Vasserman N, Tverskaya S, Polyakov A, Liem RK, Gettemans J, Robberecht W, De Jonghe P and Timmerman V (2004)  Mutant small heat-shock protein 27 causes axonal Charcot-Marie-Tooth disease and distal hereditary motor neuropathy  Nat Genet 36(6):602-6