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Brain & Development|February 23, 2016
Manifestations and characteristics of congenital adrenal hyperplasia-associated encephalopathyYuichi Abe, Tetsuro Sakai, Akihisa Okumura, et al.Brain & Development|November 26, 2015
Influence of sleep-onset time on the development of 18-month-old infants: Japan Children's cohort studyAkiko Iemura, Mizue Iwasaki, Noriko Yamakawa, et al.Brain & Development|October 3, 2015
Outcome of hemiplegic cerebral palsy born at term depends on its etiologyYukihiro Kitai, Kazuhiro Haginoya, Satori Hirai, et al.Brain & Development|December 12, 2013
Arachnoid cysts in tuberous sclerosis complexSusana Boronat, Paul Caruso, Maria Auladell, et al.Brain & Development|November 23, 2013
Clinical and magnetic resonance imaging findings in patients with Leigh syndrome and SURF1 mutationsKothari Sonam, Nahid Akthar Khan, Parayil Sankaran Bindu, et al.Brain & Development|October 12, 2013
Leigh syndrome with Fukuyama congenital muscular dystrophy: a case reportHidehito Kondo, Koichi Tanda, Chihiro Tabata, et al.Brain & Development|January 1, 1989
Increased deposition of types III and V collagen in neurofibroma tissue from patients with von Recklinghausen diseaseH Konomi, M Arima, H Tanaka, et al.Brain & Development|September 2, 2014
Effect of levetiracetam in acute encephalitis with refractory, repetitive partial seizures during acute and chronic phaseRiyo Ueda, Yoshiaki Saito, Koyo Ohno, et al.Brain & Development|August 31, 2014
Psychometric properties of the parent and teacher forms of the Japanese version of the Strengths and Difficulties QuestionnaireYuki Shibata, Kaori Okada, Rie Fukumoto, et al.Brain & Development|December 24, 2013
Intragenic mutations in SMN1 may contribute more significantly to clinical severity than SMN2 copy numbers in some spinal muscular atrophy (SMA) patientsTomoto Yamamoto, Hideyuki Sato, Poh San Lai, et al.Pageof 483