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Brain & Development|January 1, 1984
Familial porencephalic white matter disease in two generationsL M Smit, P G Barth, J Valk, et al.Brain & Development|January 1, 1983
Ondine's curse: therapeutic trial of dimeflineT Morimoto, H Nagao, H Matsuda, et al.Brain & Development|January 1, 1983
Biochemical analysis of cerebrum of fetal rat X-irradiated in utero--DNA, RNA, superoxide dismutase and lipid peroxide--H Sakuraba, H TanakaBrain & Development|January 1, 1980
Some critical notes about "the epilepsy-aphasia syndrome" in childrenM de NegriBrain & Development|March 1, 1993
Mitochondrial dysfunction in Rett syndrome. An ultrastructural and biochemical studyM T Dotti, L Manneschi, A Malandrini, et al.Brain & Development|March 1, 1993
Cerebral magnetic resonance spectroscopy in Rett syndrome. Failure to detect mitochondrial disorderJ B Nielsen, P B Toft, E Reske-Nielsen, et al.Brain & Development|March 1, 1993
Chronic subdural hematoma, as an initial manifestation of glutaric aciduria type-1H Osaka, S Kimura, A Nezu, et al.Brain & Development|March 1, 1993
Chronological SPECT studies of a patient with subacute sclerosing panencephalitisS Yagi, Y Miura, S Mizuta, et al.Brain & Development|March 1, 1993
Computed tomography and magnetic resonance imaging of affected muscle in childhood acid alpha-glucosidase deficiency: a case reportY Arai, M Osawa, K Shishikura, et al.Pageof 483