Yukie Inamori

Multicenter questionnaire survey for sporadic inclusion body myositis in Japan

Naoki Suzuki, Madoka Mori‐Yoshimura, Satoshi Yamashita et al. · Orphanet Journal of Rare Diseases · 2016 · 40 citations · Full text

Medicine, Health Sciences, Neurology +9

A new phenotype of mitochondrial disease characterized by familial late-onset predominant axial myopathy and encephalopathy

Yusuke Sakiyama, Yuji Okamoto, Itsuro Higuchi et al. · Acta Neuropathologica · 2011 · 24 citations · Full text

Medicine, Genetics, Neurology +17

The updated retrospective questionnaire study of sporadic inclusion body myositis in Japan

Naoki Suzuki, Madoka Mori‐Yoshimura, Satoshi Yamashita et al. · Orphanet Journal of Rare Diseases · 2019 · 21 citations · Full text

Medicine, Internal Medicine, Neurology +9

Mitochondrial myopathy with autophagic vacuoles in patients with the m.8344A>G mutation

Jun‐Hui Yuan, Yusuke Sakiyama, Itsuro Higuchi et al. · Journal of Clinical Pathology · 2013 · 18 citations

Life Sciences, Genetics, Pathology +17

Adult‐type metachromatic leukodystrophy with compound heterozygous <i>ARSA</i> mutations: A case report and phenotypic comparison with a previously reported case

Takehiro Hayashi, Masayuki Nakamura, Mio Ichiba et al. · Psychiatry and Clinical Neurosciences · 2011 · 13 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15