amyotrophy

n.

肌萎缩；

Neuralgic amyotrophy; the shoulder-girdle syndrome.
The clinical spectrum of neuralgic amyotrophy in 246 cases
Axonopathy and amyotrophy in mice transgenic for human four-repeat tau protein.
Mutations in SEPT9 cause hereditary neuralgic amyotrophy.
Progressive dementia, visual deficits, amyotrophy, and microinfarcts
The Bruns-Garland Syndrome (Diabetic Amyotrophy): Revisited 100 Years Later
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22
Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein
Erratum: Neurofibrillary tangles, amyotrophy and progressive motor disturbance in mice expressing mutant (P301L) tau protein (Nature...
Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex. 1994.