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Brain & Development|November 26, 2019
Atypical gamma functional connectivity pattern during light sleep in children with attention deficit hyperactivity disorderRiyo Ueda, Hiroshige Takeichi, Yoshimi Kaga, et al.
Brain & Development|December 9, 2017
Arima syndrome caused by CEP290 specific variant and accompanied with pathological cilium; clinical comparison with Joubert syndrome and its related diseasesMasayuki Itoh, Shuhei Ide, Yuji Iwasaki, et al.
Brain & Development|December 24, 2017
Novel BICD2 mutation in a Japanese family with autosomal dominant lower extremity-predominant spinal muscular atrophy-2Mieko Yoshioka, Naoya Morisada, Daisaku Toyoshima, et al.
Brain & Development|December 2, 2017
Histopathological proof of the pathogenicity of a rare GFAP mutation in a patient with flaccid paraparesisFlorian Brackmann, Roland Coras, Karl Rössler, et al.
Brain & Development|January 18, 2019
Nutritional status among women whose pregnancy outcome was afflicted with neural tube defects in Tigray region of EthiopiaAbadi Leul Welderufael, Birhane Alem Berihu, Yibrah Berhe, et al.
Brain & Development|January 1, 1988
Theta rhythms in the EEG: a genetic trait in childhood epilepsyH Doose, W K Baier
Brain & Development|March 19, 2018
Successful hemispherotomy in two refractory epilepsy patients with cerebral hemiatrophy and contralateral EEG abnormalitiesRumiko Takayama, Katsumi Imai, Hiroko Ikeda, et al.
Brain & Development|March 7, 2018
Leigh syndrome with spinal cord involvement due to a hemizygous NDUFA1 mutationAkihiko Miyauchi, Hitoshi Osaka, Masako Nagashima, et al.
Brain & Development|March 10, 2018
De novo HDAC8 mutation causes Rett-related disorder with distinctive facial features and multiple congenital anomaliesTomoko Saikusa, Munetsugu Hara, Kazuhiro Iwama, et al.
Brain & Development|July 18, 2017
Myoclonic epilepsy in infancy with preceding or concurrent afebrile generalized tonic-clonic seizures in Chinese childrenZhixian Yang, Hui Li, Jiao Xue, et al.
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