Elena Gallardo

TL;DR: Evidence and expert consensus shows an increase of musculoskeletal ultrasound indications, particularly for the shoulder, and four new A evidence levels were found for the hip, knee, ankle, and foot.

TL;DR: Clinical and MRI patterns of lower limb muscle atrophy vary with evolution of semiology in Charcot-Marie-Tooth disease type 1A, concluding that selective involvement of intrinsic foot muscles is the characteristic pattern of CMT-1A cases with minimal disease signs.

TL;DR: Closer scrutiny of nerve abnormalities beyond assessment of nerve calibre may allow for more accurate diagnostic classification of PN, as well as contribute to the understanding of the intersection of structure and function in PN.

TL;DR: It is concluded that intermediate CMT is a complex inherited syndrome, whose characterization requires a specific electrophysiological protocol comprising evaluation of upper limb proximal nerve trunks when distal CMAP amplitudes are reduced, and that an updated version of MIM phenotype numbering is needed.

TL;DR: In early GBS inflammatory oedema of spinal nerves is a pathogenically relevant feature to understanding the mechanism of ascending paralysis, particularly when conventional electrophysiological studies are normal or not diagnostic.