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Molecular Genetics and Metabolism|April 7, 1999
Clinical and molecular analysis of Japanese patients with neuronal ceroid lipofuscinosisK Oishi, H Ida, K Kurosawa, et al.
Bone|March 10, 2000
Activin release from bone coupled to bone resorption in organ culture of neonatal mouse calvariaR Sakai, Y Eto, M Hirafuji, et al.
Acta Neuropathologica|January 1, 1985
Neuropathologic study in the heterozygotes of X-linked brindled mutant mouseH Matsushima, A Okuno, Y Eto, et al.
Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|April 8, 2019
Editorial Commentary: Hip Arthroscopy Capsular Approaches: Periportal, Puncture, Interportal, T-Cut…Does It Really Matter?Stephen K Aoki
Arthroscopy : the Journal of Arthroscopic & Related Surgery : Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association|November 9, 2019
Editorial Commentary: Patient Profiling: Identifying Risk Factors That Help Predict Outcomes of Hip Arthroscopy CandidatesStephen K Aoki
European Journal of Pediatrics|February 24, 2001
Effects of enzyme replacement therapy in thirteen Japanese paediatric patients with Gaucher diseaseH Ida, O M Rennert, M Kobayashi, et al.
Brain & Development|January 1, 1991
Psychosine cytotoxicity toward rat C6 glioma cells and the protective effects of phorbol ester and dimethylsulfoxide: implications for therapy in Krabbe diseaseS Sugama, Y Eto, H Yamamoto, et al.
Pediatric Research|November 1, 1990
Psychosine cytotoxicity in rat neural cell cultures and protection by phorbol ester and dimethyl sulfoxideS Sugama, S U Kim, H Ida, et al.
European Journal of Pediatrics|October 1, 1980
Multiple sulfatase deficiency (mucosulfatidosis): impaired degradation of labeled sulfated compounds in cultured skin fibroblasts in vivoY Eto, S Numaguchi, T Tahara, et al.
Gene Therapy|August 1, 1995
Overexpression of arylsulfatase A gene in fibroblasts from metachromatic leukodystrophy patients does not induce a new phenotypeT Ohashi, R Matalon, J A Barranger, et al.
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