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Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2
This paper identifies the frequent role of HSP27 mutations in the etiology of distal hereditary motor neuropathy and motor CMT2. It also shows the implications for the pathogenesis of this gene in peripheral motor neurons.
See p. 1660; Editorial, p. 1656
Diffusion tensor imaging of the pyramidal tracts in infants with motor dysfunction
This paper demonstrates the possible clinical application of a quantitative MR marker to correlate with future neurodevelopmental outcome in infants presenting with motor dysfunction.
See p. 1676
GM1/GalNAc-GD1a complex: A target for pure motor Guillain-Barré syndrome
Antibody …
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