Art
J-GLOBAL ID:200902001968921345   Reference number:81A0172094

A new variant of Lowe oculocerebrorenal syndrome.

Lowe眼・脳・じん症候群の新しい一変種
Author (7):
Material:
Volume: 132  Issue:Page: 385-388  Publication year: Dec. 1980 
JST Material Number: G0649A  ISSN: 0040-8727  CODEN: TJEMAO  Document type: Article
Article type: 原著論文  Country of issue: Japan (JPN)  Language: ENGLISH (EN)
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JST classification (3):
JST classification
Category name(code) classified by JST.
眼の疾患一般【’81~’92】  ,  中枢神経系の疾患【’81~’92】  ,  じん臓の疾患【’81~’92】 
Reference (12):
  • 1) Brown, N. & Gardner, R. J. M. (1975) Lowe syndrome: identification of the carrier state. In: The Eye and Inborn Errors of Metabolism, Brith Defect, Orginal Article Series, XII, New York, Alan R. Liss, pp. 569-577.
  • 2) Chusorian, A. & Rowland, L. P. (1966) Lowe's syndrome, Neurology, 16, 115-122.
  • 3) Holmes, L. B., McGowan, B. L. & Efron, M. L. (1969) Lowe's syndrome. A search for the carrier state. Pediatrics, 44, 358-363.
  • 4) Kondo, T., Taniguchi, N., Taniguchi, K., Matsuda, I. & Murao, M. (1978) Inactive form of erythrocyte carbonic anhydrase B in patients with primary tubular acidosis. J. clin. Invest., 62, 610-617.
  • 5) Matsuda, I., Takeda, T., Sugai, M. & Matsuura, N. (1969) Oculocerebrorenal syndrome. In a child with a normal urinary acidification and a defect in bicarbonate reabsorption. Amer. J. Dis. Child., 117, 205-212.
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