K Misu

Late-onset familial amyloid polyneuropathy type I (transthyretin Met30-associated familial amyloid polyneuropathy) unrelated to endemic focus in Japan

K Misu, Naoki Hattori, Masaaki Nagamatsu et al. · Brain · 1999 · 172 citations · Full text

Neurological Disorder, Genetic Disorder, Neuroepidemiology +15

Age of onset influences clinical features of chronic inflammatory demyelinating polyneuropathy

Naoki Hattori, K Misu, Haruki Koike et al. · Journal of the Neurological Sciences · 2001 · 93 citations

Neurodegenerative Diseases, Aging, Ophthalmology +10

An axonal form of Charcot-Marie-Tooth disease showing distinctive features in association with mutations in the peripheral myelin protein zero gene (Thr124Met or Asp75Val)

K Misu · Journal of Neurology Neurosurgery & Psychiatry · 2000 · 90 citations · Full text

Identification of novel sequence variants in the neurofilament‐light gene in a Japanese population: analysis of Charcot‐Marie‐Tooth disease patients and normal individuals

Tsuyoshi Yoshihara, Masahiko Yamamoto, Naoki Hattori et al. · Journal of the Peripheral Nervous System · 2002 · 87 citations

Genetics, Genetic Epidemiology, Pathology +18

Mortality and morbidity in peripheral neuropathy associated Churg-Strauss syndrome and microscopic polyangiitis.

Naoki Hattori, Keiko Mori, K Misu et al. · PubMed · 2002 · 68 citations