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Brain & Development|September 1, 1993
Decreased 6-keto prostaglandin F1 alpha (6-keto PGF1 alpha) in patients with Lesch-Nyhan syndromeA Imamura, H Yamanouchi, M Arima
Brain & Development|September 1, 1993
Idiopathic lactic acidemia with developmental delay and type 1 muscle fiber atrophy: report of two patientsA Iso, N Murakami, H Yoneyama, et al.
Brain & Development|September 1, 1993
Thalamic hyperdensity--is it a diagnostic marker for Sandhoff disease?M Calişkan, M Ozmen, M Beck, et al.
Brain & Development|January 1, 1979
Cockayne syndrome: report of two siblings and review of literature in JapanK Jin, T Handa, T Ishihara, et al.
Brain & Development|January 1, 1979
Neurological complications of the ring (22) syndrome: a case reportN Sakuragawa, K Adachi, M Hayashi, et al.
Brain & Development|January 1, 1979
A case of Ullrich's disease (Kongenitale, Atonisch-Sklerotische Muskeldystrophie)K Nihei, S Kamoshita, T Atsumi
Brain & Development|January 1, 1979
Follow-up study of hypotonic forms of cerebral palsyI A Lesný
Brain & Development|August 1, 2021
Gait disturbance in a patient with de novo 1.0-kb SOX2 microdeletionHiroyuki Yamada, Tohru Okanishi, Tetsuya Okazaki, et al.
Brain & Development|January 1, 1983
Glutamic acid decarboxylase in cerebrospinal fluid in infancy and childhood Part II. Glutamic acid decarboxylase activity in cerebrospinal fluid of children with neurological diseasesH Tada
Brain & Development|January 1, 1983
Acute hemiplegia with lacunar infarct after varicella infection in childhoodI Eda, S Takashima, K Takeshita
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