M. Higashi

ANovel Mutation in ELOVL 4 Leading to Spinocerebellar Ataxia ( SCA ) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia A Broadened Spectrum of SCA 34

S. Tsuji, N. Matsumoto, S. Morishita, 2015 .

A Novel Mutation in ELOVL4 Leading to Spinocerebellar Ataxia (SCA) With the Hot Cross Bun Sign but Lacking Erythrokeratodermia: A Broadened Spectrum of SCA34.

S. Tsuji, N. Matsumoto, S. Morishita, 2015, JAMA neurology.

Prevalence and clinicoradiological features of spinocerebellar ataxia type 34 in a Japanese ataxia cohort.

H. Mizusawa, K. Ishikawa, T. Yokota, 2019, Parkinsonism & related disorders.

Thymidine Kinase 2 and Mitochondrial Protein COX I in the Cerebellum of Patients with Spinocerebellar Ataxia Type 31 Caused by Penta-nucleotide Repeats (TTCCA)n

K. Ishikawa, T. Yokota, Hanako Aoki, 2022, The Cerebellum.

Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects

H. Mizusawa, K. Ishikawa, T. Yokota, 2017, Journal of the Neurological Sciences.

Abnormal RNA structures (RNA foci) containing a penta‐nucleotide repeat (UGGAA)n in the Purkinje cell nucleus is associated with spinocerebellar ataxia type 31 pathogenesis

Y. Eishi, H. Mizusawa, E. Sugawara, 2013, Neuropathology : official journal of the Japanese Society of Neuropathology.

Elevation of 8‐hydroxy‐2′‐deoxyguanosine in the cerebrospinal fluid of three patients with superficial siderosis

H. Mizusawa, A. Okawa, T. Hattori, 2015 .

A diagnostic decision tree for adult cerebellar ataxia based on pontine magnetic resonance imaging

M. Tomita, H. Mizusawa, T. Hattori, 2018, Journal of the Neurological Sciences.

Sequence configuration of spinocerebellar ataxia type 8 repeat expansions in a Japanese cohort of 797 ataxia subjects

H. Mizusawa, K. Ishikawa, T. Yokota, 2017, Journal of the Neurological Sciences.