Y. Hokezu

发表

Clinical and genetic characterization of 16q-linked autosomal dominant spinocerebellar ataxia in South Kyushu, Japan

K. Arimura, R. Hirano, H. Takashima, 2009, Journal of Human Genetics.

Predisposing chromosome for spinocerebellar ataxia type 6 (SCA6) in Japanese

M. Nishizawa, Y. Takiyama, K. Tashiro, 2001, Journal of medical genetics.

[A amyotrophic lateral sclerosis (ALS) 4 family misdiagnosed as hereditary spastic paraplegia-a case report].

E. Matsuura, H. Takashima, Y. Hokezu, 2017, Rinsho shinkeigaku = Clinical neurology.

Five novel SLC7A7 variants and y+L gene‐expression pattern in cultured lymphoblasts from Japanese patients with lysinuric protein intolerance

K. Ihara, T. Hara, A. Nakai, 2002, Human Mutation.

Long-term safety and efficacy of patisiran for hereditary transthyretin-mediated amyloidosis with polyneuropathy: 12-month results of an open-label extension study

E. Nordh, Yi-Chung Lee, R. Sommerville, 2020, Lancet Neurology.

Familial spastic paraplegia with mental impairment and thin corpus callosum

A. Nakamura, M. Nakagawa, S. Izumo, 1995, Journal of the Neurological Sciences.

Myopathy in a patient with systemic AA amyloidosis possibly induced by psoriasis vulgaris: An autopsy case

K. Obayashi, I. Higuchi, Y. Maki, 2015, Muscle & nerve.

[Pure trigeminal motor neuropathy with an antecedent infection: a case report].

J. Fukae, Y. Tsuboi, J. Tsugawa, 2014, Rinsho shinkeigaku = Clinical neurology.

[Two cases of syringomyelia showing atypical neurological sings].

Y. Takiyama, Y. Hokezu, K. Nagamatsu, 1985, Rinshō shinkeigaku Clinical neurology.

[A family case of HAM and HTLV-I carrier including two sisters presenting with myositis].

I. Higuchi, M. Nagai, Y. Hokezu, 1994, Rinshō shinkeigaku Clinical neurology.

Creation and validation of a bladder dysfunction symptom score for HTLV-1-associated myelopathy/tropical spastic paraparesis

J. Kira, H. Yonezawa, Takahiko Ueno, 2020, Orphanet Journal of Rare Diseases.

[Two cases of POEMS syndrome with increased vascular endothelial growth factor (VEGF)].

I. Maruyama, K. Arimura, O. Watanabe, 1997, Rinsho shinkeigaku = Clinical neurology.

[A familial case of spinocerebellar ataxia type 8 (SCA 8)--its clinical findings and an issue about the genetic basis].

Y. Takiyama, K. Sakoe, Y. Hokezu, 2000, Rinsho shinkeigaku = Clinical neurology.