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American Journal of Diseases of Children (1960)|March 1, 1981
Histidinemia: biochemical parameters for diagnosisF Ito, K Aoki, Y EtoNihon Rinsho. Japanese Journal of Clinical Medicine|December 1, 1995
[Metachromatic leukodystrophy (MLD) and Multiple sulphatase deficiency (MSD)]Y Eto, Y Hasegawa, T TsudaJournal of Lipid Research|September 1, 1971
Lipid composition of rat brain myelin in triethyl tin-induced edemaY Eto, K Suzuki, K SuzukiBiochemical and Biophysical Research Communications|February 17, 1998
Activin A: a commitment factor in erythroid differentiationM Shiozaki, M Kosaka, Y EtoBrain & Development|January 1, 1989
Fetal GM1-gangliosidosis: morphological and biochemical studiesH Ida, Y Eto, K MaekawaHuman Cell|June 1, 1989
[Application of neuronal cell culture in human degenerative brain disorders]Y Eto, H Ida, K MatsuiBrain & Development|September 1, 1996
Two novel mutations in a Japanese patient with the late-infantile form of metachromatic leukodystrophyT Tsuda, Y Hasegawa, Y EtoPediatric Neurology|November 13, 2001
Magnetic resonance imaging in three children with kernicterusS Sugama, A Soeda, Y EtoEuropean Journal of Pediatrics|November 1, 1979
Urinary acid mucopolysaccharides in multiple sulfatase deficiency (mucosulfatidosis)Y Eto, S Numaguchi, T HandaJournal of Craniofacial Genetics and Developmental Biology|March 24, 2000
Pfeiffer syndrome caused by haploinsufficient mutation of FGFR2M Tsukuno, H Suzuki, Y EtoPageof 127