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The Tohoku Journal of Experimental Medicine|February 1, 1985
Pathochemical study of a case of hereditary cerebral degenerative disease--lipopigment accumulation and peroxidase deficiency in brainS Yamaguchi, A Okuno, Y Eto, et al.The Tohoku Journal of Experimental Medicine|April 1, 1986
Abnormal excretion of autofluorescent lipids in urine from patients with neuronal ceroid lipofuscinosisT Ohashi, Y Kanamoto, S Yamaguchi, et al.American Journal of Medical Genetics. Supplement|January 1, 1988
Clinical and biochemical studies of Japanese neuronal ceroid-lipofuscinosisY Eto, T Tsuda, T Ohhashi, et al.Archives of Neurology|January 1, 1982
Prenatal diagnosis of metachromatic leukodystrophy: a diagnosis by amniotic fluid and its confirmationY Eto, T Tahara, N Koda, et al.Journal of Inherited Metabolic Disease|June 23, 2000
Gene therapy/cell therapy for lysosomal storage diseaseY Eto, T OhashiJournal of Biochemistry|November 1, 1983
A comparative study of brain arylsulfatases B1 and B2: the difference between the two forms in rates of uptake by multiple sulfatase deficient (MSD) disorder fibroblastsY Kureha, Y EtoJournal of Enzyme Inhibition|January 1, 1993
Indirect strong inhibition by acid-stable trypsin-plasmin inhibitor (ASTPI) of the activations of elastase and plasma fibrinolysis in a dog model of acute pancreatitisH Sumi, Y EtoNeurochemical Research|February 11, 1999
Clinical and molecular characteristics of Japanese Gaucher diseaseY Eto, H IdaNihon Rinsho. Japanese Journal of Clinical Medicine|August 1, 1992
[Function, molecular structure and gene expression regulation of erythroid differentiation factor (EDF/activin A)]M Shiozaki, Y EtoPageof 127