Length-dependent MRI of hereditary neuropathy with liability to pressure palsies.
Michael D PridmoreRyan CastoroMegan Simmons McCollumHakmook KangJun LiRichard DortchPublished in: Annals of clinical and translational neurology (2019)
Despite the multifocal nature of the HNPP phenotype, muscle Fper measurements relate to disability and exhibit a proximal-to-distal gradient consistent with length-dependent axonal loss, suggesting that Fper may be a viable biomarker of disease progression in HNPP.