Biomedical subjects
J Onisawa
Publications and source records attributed to J Onisawa.
Morphological and biochemical studies of a case of mucopolysaccharidosis II (Hunter's syndrome).
An autopsy case of a 19-year-old boy who had shown typical gargoyle features, strictly consistent with mucopolysaccharidosis type II (Hunter's syndrome) was reported. Histologically, cytoplasmic vacuolar change was found in hepatocytes, sinusoidal epithelium of spleen, follicular cells of thyroid, Sertoli cells of testis, chromophobe cell of pituitary and generalized fibroblast-like cells including meninges, cardiac valve and periosteum. The vacuoles consisting of membrane-bound structures with flocculus protein-like material and occasional electron dense bodies on electron microscopy, were considered to be the site of mucopolysaccharide deposition by histochemical analysis. Deposition of lipid material consistent with so-called membranous cytoplasmic body was observed in the neurons of central, peripheral and autonomic nervous system. Hepatosplenomegaly could be explained by cytoplasmic deposition, but the cause of cardiomegaly remained further to be studied. Biochemically hepatic mucopolysaccharide was identified as heparan sulfate, while in the kidney dermatan sulfate and heparan sulfate were detected. The correlation between morphology and biochemistry, and between deposition and degeneration was discussed.
[Diagnosis of hereditary mucopolysaccharidoses].
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Chondroitin 4- and 6-sulfaturia in Morquio-Ullrich's syndrome.
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Increased urinary excretion of chondroitin sulfate A and C in Hunter's syndrome.
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Biochemical studies of urinary acid mucopolysaccharide--peptide complexes in Hurler's syndrome.
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Clinical and therapeutic aspects of the Lesch-Nyhan syndrome in Japanese children.
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Effect of prednisolone on urinary acid mucopolysaccharides excretion in genetic mucopolysaccharidoses.
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Effects of vitamins A and C on urinary excretion of acid mucopolysaccharides in the Hurler's syndrome.
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[Progress in diagnosis of inborn errors of metabolism].
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The urinary acid mucopolysaccharide-peptide complexes in normal children.
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Increased excretion of umbelliferone in phenylketonuria.
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Phenylketonuric mother without mental retardation and her two phenylketonuric children.
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The oculo-cerebro-renal syndrome in a Japanese child.
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[Symposium on clinical aspects on porphyrias. (4). The role of citric acid cycle turnover in the control of heme biosynthesis].
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The role of succinyl-CoA synthetase in the control of heme biosynthesis.
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Amino-aciduria in osteogenesis imperfecta.
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Amino-aciduria in Alport's syndrome.
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