Satoko Miyatake

49PUBLICATIONS
207CO-AUTHORS
Neurology and neuromuscular diseasesAutoimmunityGene expression (incl. microarray and other genome-wide approaches)NeurogeneticsTe puoro me ngā mahi a te rēhia o te Māori (Māori music and performing arts)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (49)

|Aug 18, 2026
Clinical features of four unrelated Japanese patients with autosomal recessive spinocerebellar ataxia type 32.

|Aug 07, 2026
An N-terminal CDC42 T43I variant reveals the mechanism of pyrin inflammasome activation.

|Jul 16, 2026
Clinical and molecular expansion of SSR4-CDG: an adult patient and pathogenic interpretation of an in-frame variant.

|Jul 01, 2026
Haplotype analysis of spinocerebellar ataxia type 36 suggests a shared permissive core haplotype across populations.

|Feb 23, 2026
Mexiletine prevents transient heart failure in a polymicrogyria child with an ATP1A3 variant: a case report.

Mai Aida, Junichi Ozawa, Yuya Takahashi

|Feb 05, 2026
TBK1-Associated Primary Lateral Sclerosis Followed by Right Temporal Variant Frontotemporal Dementia.

Tomoyasu Matsubara, Naoki Kihara, Satoko Miyatake

Pageof 9

Frequent Collaborators

45 joint publications

Naomichi Matsumoto

29 joint publications

Takeshi Mizuguchi

29 joint publications

Yuri Uchiyama

28 joint publications

Naomi Tsuchida