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Molecular Microbiology|November 28, 2002
TlpC, a novel chemotaxis protein in Rhodobacter sphaeroides, localizes to a discrete region in the cytoplasmG H Wadhams, A C Martin, S L Porter, et al.Annals of Neurology|July 25, 2006
Proteasomal inhibition causes loss of nigral tyrosine hydroxylase neuronsAnthony H V Schapira, Michael W J Cleeter, John R Muddle, et al.Neuromuscular Disorders : NMD|June 30, 2006
Clinical spectrum of CMT4C disease in patients homozygous for the p.Arg1109X mutation in SH3TC2Jaume Colomer, Rebecca Gooding, Dora Angelicheva, et al.Neuromuscular Disorders : NMD|March 11, 2009
The phenotype of Charcot-Marie-Tooth disease type 4C due to SH3TC2 mutations and possible predisposition to an inflammatory neuropathyHenry Houlden, Matilde Laura, Lionel Ginsberg, et al.Journal of Anatomy|July 2, 2002
Comparison of a new pmp22 transgenic mouse line with other mouse models and human patients with CMT1AA M Robertson, J Perea, A McGuigan, et al.Journal of Neurology, Neurosurgery, and Psychiatry|September 30, 2008
The use of nerve and muscle biopsy in the diagnosis of vasculitis: a 5 year retrospective studyD L H Bennett, M Groves, J Blake, et al.Brain : a Journal of Neurology|November 11, 2003
Coexistent hereditary and inflammatory neuropathyLionel Ginsberg, Omar Malik, Anthony R Kenton, et al.Journal of Neuropathology and Experimental Neurology|April 14, 2011
Myelin and axon pathology in a long-term study of PMP22-overexpressing miceCamiel Verhamme, Rosalind H M King, Anneloor L M A ten Asbroek, et al.Human Molecular Genetics|April 30, 2002
YAC transgenic mice carrying pathological alleles of the MJD1 locus exhibit a mild and slowly progressive cerebellar deficitCemal K Cemal, Christopher J Carroll, Lorraine Lawrence, et al.Diabetologia|February 25, 2005
Sural nerve pathology in diabetic patients with minimal but progressive neuropathyR A Malik, S Tesfaye, P G Newrick, et al.Pageof 3