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Pediatric Neurology|February 15, 2026
Motor Function Changes in Duchenne Muscular Dystrophy: A Case Series Using Conventional and Spinal Muscular Atrophy-Based Assessments During Viltolarsen TreatmentHideyuki Iwayama, Shingo Numoto, Yoshiteru Azuma, et al.
Brain & Development|June 18, 2018
Is hiragana decoding impaired in children with periventricular leukomalacia?Naoko Kurahashi, Yukiko Futamura, Norie Nonobe, et al.
Pediatric Diabetes|September 30, 2016
Molecular and clinical features of KATP -channel neonatal diabetes mellitus in JapanYukiko Hashimoto, Sumito Dateki, Masakazu Hirose, et al.
Pediatric Neurology|September 7, 2014
Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusionNaoko Kurahashi, Takeshi Tsuji, Toru Kato, et al.
Epilepsy & Behavior Reports|January 25, 2021
Association of early-onset epileptic encephalopathy with involuntary movements - Case series and literature reviewAtsuko Arisaka, Mitsuko Nakashima, Satoko Kumada, et al.
Brain & Development|June 25, 2018
A patient with a GNAO1 mutation with decreased spontaneous movements, hypotonia, and dystonic featuresAkihisa Okumura, Koichi Maruyama, Mami Shibata, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 7, 2007
Delayed neurological signs following isolated parasagittal injury in asphyxia at termYoshiaki Sato, Masahiro Hayakawa, Osuke Iwata, et al.
Brain & Development|November 20, 2013
Characteristics of epilepsy occurring in the first four monthsTatsuya Fukasawa, Motomasa Suzuki, Toru Kato, et al.
Brain & Development|April 14, 2017
Characteristics of epilepsy in patients with Kabuki syndrome with KMT2D mutationsNaoko Kurahashi, Noriko Miyake, Seiji Mizuno, et al.
American Journal of Medical Genetics. Part A|November 21, 2012
Clinical and radiological features of Japanese patients with a severe phenotype due to CASK mutationsJun-ichi Takanashi, Nobuhiko Okamoto, Yuto Yamamoto, et al.
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