Kota Sato

  • 439 Citations
  • 12 h-Index
20112019
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Research Output 2011 2019

  • 439 Citations
  • 12 h-Index
  • 100 Article
  • 12 Letter
  • 1 Conference contribution
  • 1 Comment/debate

Acute anti-inflammatory markers ITIH4 and AHSG in mice brain of a novel Alzheimer's disease model

Shi, X., Ohta, Y., Liu, X., Shang, J., Morihara, R., Nakano, Y., Feng, T., Huang, Y., Sato, K., Takemoto, M., Hishikawa, N., Yamashita, T. & Abe, K., Jan 1 2019, In : Journal of Alzheimer's Disease. 68, 4, p. 1667-1675 9 p.

Research output: Contribution to journalArticle

alpha-2-HS-Glycoprotein
Alzheimer Disease
Anti-Inflammatory Agents
Brain
Thalamus

A rare case of klinefelter syndrome accompanied by spastic paraplegia and peripheral neuropathy

Sasaki, R., Ohta, Y., Takahashi, Y., Tsunoda, K., Tadokoro, K., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T. & Abe, K., Jan 1 2019, In : Internal Medicine. 58, 3, p. 437-440 4 p.

Research output: Contribution to journalArticle

Klinefelter Syndrome
Paraplegia
Peripheral Nervous System Diseases
Chromosome Disorders
Motor Evoked Potentials

Asymmetrical and isolated hypoglossal nerve palsy accompanied by a new subset of anti-ganglioside antibodies in a patient with diffuse large b cell lymphoma

Ohta, Y., Kawahara, Y., Tadokoro, K., Sato, K., Sasaki, R., Takahashi, Y., Takemoto, M., Hishikawa, N., Yamashita, T., Asano, T., Inomata, T. & Abe, K., Jan 15 2019, In : Internal Medicine. 58, 2, p. 283-286 4 p.

Research output: Contribution to journalArticle

Hypoglossal Nerve Diseases
Lymphoma, Large B-Cell, Diffuse
Gangliosides
Anti-Idiotypic Antibodies
Lymphoma
1 Citation (Scopus)

A unique Japanese CPEO family with a novel homozygous m.14819 T > G (p. S25A) substitution

Nomura, E., Ohta, Y., Tadokoro, K., Sato, K., Sasaki, R., Takahashi, Y., Yamashita, T., Takemoto, M., Hishikawa, N., Goto, Y. I. & Abe, K., May 15 2019, In : Journal of the neurological sciences. 400, p. 145-147 3 p.

Research output: Contribution to journalLetter

Chronic Progressive External Ophthalmoplegia
Mitochondrial DNA

Characteristic Clinical Features of Werner Syndrome with a Novel Compound Heterozygous WRN Mutation c.1720+1G>A Plus c.3139-1G>C

Matsumoto, N., Ohta, Y., Deguchi, K., Kishida, M., Sato, K., Shang, J., Takemoto, M., Hishikawa, N., Yamashita, T., Watanabe, A., Yokote, K., Takemoto, M., Oshima, J. & Abe, K., Apr 1 2019, In : Internal medicine (Tokyo, Japan). 58, 7, p. 1033-1036 4 p.

Research output: Contribution to journalArticle

Open Access
Werner Syndrome
Mutation
Marriage
Parents
Phenotype