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Brain & Development|September 14, 2000
Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndromeY Saito, S TakashimaBrain & Development|September 14, 2000
REM sleep atonia: responsible brain regions, quantification, and clinical implicationJ KohyamaBrain & Development|November 15, 2017
A novel temporal pattern of childhood cerebral X-linked adrenoleukodystrophyEmanuela C Turco, Francesca Ormitti, Anna Andreolli, et al.Brain & Development|October 3, 2017
The presence of diminished white matter and corpus callosal thinning in a case with a SOX9 mutationAyumi Matsumoto, Eri Imagawa, Noriko Miyake, et al.Brain & Development|January 1, 1988
Interactions of ACTH4-10 and ACTH1-24 with L-[3H]glutamate binding sites and GABA/benzodiazepine/picrotoxin receptor complexes in vitroM Ito, O Yu, T H ChiuBrain & Development|February 12, 2018
Familial cases of progressive myoclonic epilepsy caused by maternal somatic mosaicism of a recurrent KCNC1 p.Arg320His mutationHyuna Kim, Sangmoon Lee, Murim Choi, et al.Brain & Development|December 4, 2018
Sensory processing in children with autism spectrum disorder and the mental health of primary caregiversKanae Suzuki, Shu Takagai, Masatsugu Tsujii, et al.Brain & Development|December 6, 2018
Age related signal changes of the pituitary stalk on thin-slice magnetic resonance imaging in infantsTakashi Okazaki, Tetsu Niwa, Keiji Suzuki, et al.Brain & Development|November 11, 2019
A new missense mutation in DPF2 gene related to Coffin Siris syndrome 7: Description of a mild phenotype expanding DPF2-related clinical spectrum and differential diagnosis among similar syndromes epigenetically determinedRoberta Milone, Maria Gnazzo, Elena Stefanutti, et al.Brain & Development|February 12, 2019
MELAS syndrome with m.4450 G > A mutation in mitochondrial tRNAMet geneMari Kuwajima, Masahide Goto, Koyuru Kurane, et al.Pageof 483