A. Kawakami

Clinical and genetic characterizations of 16q‐linked autosomal dominant spinocerebellar ataxia (AD‐SCA) and frequency analysis of AD‐SCA in the Japanese population

M. Nishizawa, T. Ikeuchi, O. Onodera, 2007, Movement disorders : official journal of the Movement Disorder Society.

Thalamic form of Creutzfeldt-Jakob disease or fatal insomnia? Report of a sporadic case with normal prion protein genotype

S. Tsuji, K. Kawasaki, K. Wakabayashi, 1997, Acta Neuropathologica.

Acute relapsing encephalopathy mimicking acute necrotizing encephalopathy in a 4-year-old boy

M. Miyao, M. Momoi, T. Yamagata, 1999, Brain and Development.

Co-existence of spastic paraplegia-30 with novel KIF1A mutation and spinocerebellar ataxia 31 with intronic expansion of BEAN and TK2 in a family

Y. Takiyama, N. Hara, T. Ikeuchi, 2017, Journal of the Neurological Sciences.

Clinical diagnosis of MM2-type sporadic Creutzfeldt-Jakob disease

T. Sato, Y. Shiga, H. Mizusawa, 2005, Neurology.

Fulminant bowel‐associated dermatosis‐arthritis syndrome that clinically showed necrotizing fasciitis‐like severe skin and systemic manifestations

K. Saga, K. Jimbow, H. Takahashi, 2006, Journal of the European Academy of Dermatology and Venereology : JEADV.