Yoshida Kunihiro | Department of Brain Disease Research, Shinshu University School of Medicine, Japan

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概要

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著作論文

Biopsy-proven Tuberculous Meningitis Mimicking CNS Sarcoidosis
Huntington's disease with onset ages greater than 60 years
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in Nagano
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan
A Japanese case of SCA14 with the Gly128Asp mutation
Spinal Epidural Abscess with Osteomyelitis as a Cause of Bacterial Meningitis
A novel nonsense mutation in a Japanese family with ataxia with oculomotor apraxia type 2 (AOA2)
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) gene
Criteria for Early Identification of Aceruloplasminemia
Early Involvement of the Corpus Callosum in a Patient with Hereditary Diffuse Leukoencephalopathy with Spheroids Carrying the de novo K793T Mutation of CSF1R
Corpus Callosum Atrophy in Patients with Hereditary Diffuse Leukoencephalopathy with Neuroaxonal Spheroids: An MRI-based Study

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