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Brain & Development|October 22, 2013
A haploinsufficiency of FOXG1 identified in a boy with congenital variant of Rett syndromeAkira Kumakura, Satoru Takahashi, Kazuki Okajima, et al.
Pediatric Neurology|October 29, 2003
A patient with epilepsia partialis continua with anti-glutamate receptor epsilon 2 antibodiesAkira Kumakura, Tomoko Miyajima, Tatsuya Fujii, et al.
Brain & Development|August 22, 2016
Two mild cases of Dravet syndrome with truncating mutation of SCN1AToru Takaori, Akira Kumakura, Atsushi Ishii, et al.
Pediatric Neurology|December 7, 2007
Split notochord syndrome with congenital unilateral Horner's signAkira Kumakura, Tadamori Takahara, Junko Asada, et al.
Pediatric Neurology|September 15, 2009
Diffusion-weighted imaging in preclinical Leigh syndromeAkira Kumakura, Junko Asada, Ryosuke Okumura, et al.
Pediatric Neurology|October 18, 2011
Pandemic influenza A-associated acute necrotizing encephalopathy without neurologic sequelaeAkira Kumakura, Chihiro Iida, Makiko Saito, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 30, 2017
Herpes zoster meningitis in immunocompetent children: Two case reports and a literature reviewNaohiro Itoh, Kouji Motokura, Akira Kumakura, et al.
Intractable & Rare Diseases Research|December 19, 2018
Identification of a rare homozygous SZT2 variant due to uniparental disomy in a patient with a neurodevelopmental disorderTaichi Imaizumi, Akira Kumakura, Keiko Yamamoto-Shimojima, et al.
No to Hattatsu = Brain and Development|November 25, 2003
[Intractable epilepsy (apneic seizure) in an infant with 18q deletion syndrome]Tomohiro Kumada, Masatoshi Ito, Tomoko Miyajima, et al.
Brain & Development|July 18, 2008
Novel de novo splice-site mutation of SCN1A in a patient with partial epilepsy with febrile seizures plusAkira Kumakura, Masatoshi Ito, Daisuke Hata, et al.
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