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Fingerprint Fingerprint is based on mining the text of the person's scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 8 Similar Profiles
Brain Diseases Medicine & Life Sciences
Mutation Medicine & Life Sciences
Seizures Medicine & Life Sciences
Genes Medicine & Life Sciences
Subacute Sclerosing Panencephalitis Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Exome Medicine & Life Sciences
Febrile Seizures Medicine & Life Sciences

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Research Output 1998 2019

  • 1210 Citations
  • 20 h-Index
  • 74 Article
  • 2 Comment/debate
  • 2 Review article
  • 1 Conference article

An acute encephalopathy with reduced diffusion in BRAF-associated cardio-facio-cutaneous syndrome

Okuzono, S., Fukai, R., Noda, M., Miyake, N., Lee, S., Kaku, N., Sanefuji, M., Akamine, S., Kanno, S., Ishizaki, Y., Torisu, H., Kira, R., Matsumoto, N., Sakai, Y. & Ohga, S., Apr 1 2019, In : Brain and Development. 41, 4, p. 378-381 4 p.

Research output: Contribution to journalArticle

Brain Diseases
Exome
Mutation
Inborn Genetic Diseases
Sick Leave

A nationwide survey on tracheostomy for very-low-birth-weight infants in Japan

on behalf of the Neonatal Research Network of Japan, Jan 1 2019, In : Pediatric Pulmonology. 54, 1, p. 53-60 8 p.

Research output: Contribution to journalArticle

Very Low Birth Weight Infant
Tracheostomy
Japan
Odds Ratio
Parturition

Early Intervention With Adrenocorticotropin for Acute Encephalopathy-Associated Epileptic Spasms: Report of Two Cases

Yonemoto, K., Shono, Y., Sanefuji, M., Kaku, N., Sakata, A., Baba, R., Yamashita, F., Akamine, S., Torio, M., Ishizaki, Y., Maehara, Y., Sakai, Y. & Ohga, S., Jan 1 2019, In : Clinical EEG and Neuroscience. 50, 1, p. 51-55 5 p.

Research output: Contribution to journalArticle

Spasm
Brain Diseases
Adrenocorticotropic Hormone
Electroencephalography
Sick Leave
Dental Pulp
Dopaminergic Neurons
Brain-Derived Neurotrophic Factor
Neurites
Attention Deficit Disorder with Hyperactivity

Recurrent de novo MAPK8IP3 variants cause neurological phenotypes

Iwasawa, S., Yanagi, K., Kikuchi, A., Kobayashi, Y., Haginoya, K., Matsumoto, H., Kurosawa, K., Ochiai, M., Sakai, Y., Fujita, A., Miyake, N., Niihori, T., Shirota, M., Funayama, R., Nonoyama, S., Ohga, S., Kawame, H., Nakayama, K., Aoki, Y., Matsumoto, N. & 4 othersKaname, T., Matsubara, Y., Shoji, W. & Kure, S., Jun 1 2019, In : Annals of Neurology. 85, 6, p. 927-933 7 p.

Research output: Contribution to journalArticle

Adaptor Protein Complex 1
Axons
Phenotype
Kinesin
Axonal Transport