Disease: Hereditary myopathy with intranuclear filamentous
- Amyloid filaments in inclusion body myositis. Novel findings provide insight into nature of filaments
- Autosomal dominant distal myopathy: further evidence of a chromosome 14 locus
- Early-onset Alzheimers and cortical vision impairment in a woman with valosin-containing protein disease associated with 2 APOE ε4/APOE ε4 genotype
- Gene-related protein surplus myopathies
- Intranuclear and cytoplasmic filamentous inclusions in distal myopathy (Welander)