Disease: Neuropathy- hereditary motor and sensory- Okinawa type
- A new type of hereditary motor and sensory neuropathy linked to chromosome 3
- Brainstem and spinal cord motor neuron involvement with optineurin inclusions in proximal-dominant hereditary motor and sensory neuropathy
- Clinical features of inherited neuropathy with BSCL2 mutations in Japan
- Clinical report of hereditary motor and sensory neuropathy with proximal dominance in Shiga prefecture
- Hereditary motor and sensory neuropathy Okinawa type mimicking proximal myopathy
- History of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P)
- HMSN-P caused by p.Pro285Leu mutation in TFG is not confined to patients with Far East ancestry
- Mutations in COA7 cause spinocerebellar ataxia with axonal neuropathy
- Optinurin inclusions in proximal hereditary motor and sensory neuropathy (HMSN-P): familial amyotrophic lateral sclerosis with sensory neuronopathy?
- Recurrent takotsubo cardiomyopathy within a short span of time in a patient with hereditary motor and sensory neuropathy
- Refinement of a locus for autosomal dominant hereditary motor and sensory neuropathy with proximal dominancy (HMSN-P) and genetic heterogeneity
- Survey of patients with advanced-stage Okinawa-type neurogenic muscular atrophy (hereditary motor and sensory neuropathy with proximal dominant involvement: HMSN-P)
- The natural history of hereditary motor and sensory neuropathy with proximal dominant involvement (HMSN-P) in 97 Japanese patients