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Brain & Development|September 14, 2000
Dopamine deficiency in miceK Kobayashi, H Sano
Brain & Development|September 14, 2000
Gene mutation in hereditary progressive dystonia with marked diurnal fluctuation (HPD), strictly defined dopa-responsive dystoniaN Nishiyama, S Yukishita, H Hagiwara, et al.
Brain & Development|September 14, 2000
Autosomal recessive juvenile parkinsonismM Saito, M Maruyama, K Ikeuchi, et al.
Brain & Development|September 14, 2000
Diagnosis and treatment of 6-pyruvoyl-tetrahydropterin synthase deficiencyH Shintaku, M Asada, Y Sawada
Brain & Development|September 14, 2000
Neurotransmitter changes in the pathophysiology of Lesch-Nyhan syndromeY Saito, S Takashima
Brain & Development|September 14, 2000
REM sleep atonia: responsible brain regions, quantification, and clinical implicationJ Kohyama
Brain & 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 Chiu
Brain & 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.
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