Takashi Shibata

  • 66 Citations
  • 5 h-Index
20122019
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  • 6 Similar Profiles
Seizures Medicine & Life Sciences
Partial Epilepsy Medicine & Life Sciences
Electroencephalography Medicine & Life Sciences
Cerebrospinal fluid Chemical Compounds
Epilepsy Medicine & Life Sciences
Scalp Medicine & Life Sciences
Pyridoxic Acid Medicine & Life Sciences
Infantile Spasms Medicine & Life Sciences

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Research Output 2012 2019

  • 66 Citations
  • 5 h-Index
  • 20 Article
  • 2 Review article
1 Citation (Scopus)

Anti-NMDA-receptor antibody in initial diagnosis of mood disorder

Kawai, H., Takaki, M., Sakamoto, S., Shibata, T., Tsuchida, A., Yoshimura, B., Yada, Y., Matsumoto, N., Sato, K., Abe, K., Okahisa, Y., Kishi, Y., Takao, S., Tsutsui, K., Kanbayashi, T., Tanaka, K. & Yamada, N., Jan 1 2019, In : European Neuropsychopharmacology.

Research output: Contribution to journalArticle

N-Methyl-D-Aspartate Receptors
Mood Disorders
Antibodies
Immunoglobulin G
Anti-N-Methyl-D-Aspartate Receptor Encephalitis
1 Citation (Scopus)
Scalp
Electroencephalography
Seizures
Stroke
Pediatrics

Epileptic high-frequency oscillations in scalp electroencephalography

Shibata, T. & Kobayashi, K., Jan 1 2018, In : Acta Medica Okayama. 72, 4, p. 325-329 5 p.

Research output: Contribution to journalArticle

Electroencephalography
Scalp
Epilepsy
Rolandic Epilepsy
Infantile Spasms
2 Citations (Scopus)

Ethosuximide-induced Stevens-Johnson syndrome: Beneficial effect of early intervention with high-dose corticosteroid therapy

Tachibana, K., Hamada, T., Tsuchiya, H., Shibata, T., Fujii, K., Kobayashi, K. & Iwatsuki, K., Jan 1 2018, (Accepted/In press) In : Journal of Dermatology.

Research output: Contribution to journalArticle

Ethosuximide
Stevens-Johnson Syndrome
Adrenal Cortex Hormones
Cheek
Methylprednisolone
9 Citations (Scopus)

Loss-of-function and gain-of-function mutations in PPP3CA cause two distinct disorders

Mizuguchi, T., Nakashima, M., Kato, M., Okamoto, N., Kurahashi, H., Ekhilevitch, N., Shiina, M., Nishimura, G., Shibata, T., Matsuo, M., Ikeda, T., Ogata, K., Tsuchida, N., Mitsuhashi, S., Miyatake, S., Takata, A., Miyake, N., Hata, K., Kaname, T., Matsubara, Y. & 2 others, Saitsu, H. & Matsumoto, N., Apr 15 2018, In : Human Molecular Genetics. 27, 8, p. 1421-1433 13 p.

Research output: Contribution to journalArticle

Open Access
Mutation
Calcineurin
Catalytic Domain
Arthrogryposis
Multiple Abnormalities