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  • 脳神経精神医学講座 (国立精神・神経医療研究センター)

医科学専攻

  • Doctoral Courses 
    博士課程

Neurological and Psychiatric Sciences /(National Center of Neurology and Psychiatry)脳神経精神医学講座 (国立精神・神経医療研究センター)

  • 臨床神経学
  • 分子遺伝学
  • 神経変性疾患

STAFF

Professor

  • Takahashi, YujiProfessor. 高橋 祐二 教授

CONTACT

TEL:+81-42-341-2711
E-MAIL:yutakahashi*ncnp.go.jp
(「*」を「@」に変換してください)

OUTLINE

We conduct integrated basic and clinical researches for neurological disorders. The aims of our researches are to elucidate causes of neurological disorders based on genomic analysis and to conduct clinical researches based on the established molecular diagnosis.

脳神経内科疾患の臨床・基礎の統合的研究を行います。ゲノム解析を基盤とした脳神経疾患の原因解明を行い、確定した病型に基づく臨床研究を展開します。

ARTICLE

Odo T et al. Blended phenotype of adult-onset Alexander disease and spinocerebellar ataxia type 6. Neurol Genet. 2020;6(6):e522.
URL:https://www.ncbi.nlm.nih.gov/pubmed/33134518

Ishihara T et al. Neuronal intranuclear inclusion disease presenting with an MELAS-like episode in chronic polyneuropathy. Neurol Genet. 2020;6(6):e531.
URL:http://ng.neurology.org/content/6/6/e531.abstract

Takahashi Y et al. Altered immunoreactivity of ErbB4, a causative gene product for ALS19, in the spinal cord of patients with sporadic ALS. Neuropathology. 2019;39(4):268-78.
URL:https://www.ncbi.nlm.nih.gov/pubmed/31124187

Takahashi Y et al. Compound heterozygous intermediate MJD alleles cause cerebellar ataxia with sensory neuropathy. Neuro Genet. 2016;3(1):e123.
URL:http://www.ncbi.nlm.nih.gov/pubmed/27896316

Takahashi Y et al. ERBB4 mutations that disrupt the neuregulin-ErbB4 pathway cause amyotrophic lateral sclerosis type 19. Am J Hum Genet. 2013;93(5):900-5.
URL:http://www.ncbi.nlm.nih.gov/pubmed/24119685

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