Low urinary excretion of heparan sulfate in three patients with Lowe's syndrome

Author:

Yokoi T.,Uozaki T.,Kasei M.,Sato T.,Taniguchi N.

Publisher

Elsevier BV

Subject

Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine

Reference18 articles.

1. Organic aciduria, decreased renal ammonia production, hydroophthalmos, and mental retardation. A clinical study;Lowe;Am. J. Dis. Child.,1952

2. Über die Ausscheidung saurer Mucopolysaccharide bei einem Kind mit Lowe-Syndrom;Suschke;Mschr. Kinderheilk.,1969

3. Urinary excretion of acid glycosaminoglycans and hydroxyproline in a patient with oculo-cerebro-renal syndrome;Hayashi;Tohoku J. Exp. Med.,1978

4. Urinary acid glycosaminoglycans in a patient with oculo-cerebro-renal syndrome;Hayashi;Tohoku J. Exp. Med.,1978

5. Urinary excretion of a large amount of bound sialic acid and of undersulfated chondroitin sulfate A by patients with the Lowe syndrome;Akasaki;Clin. Chim. Acta,1978

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Unusual renal features of Lowe syndrome in a mildly affected boy;American Journal of Medical Genetics;2000-12-18

2. Lowe Oculocerebrorenal Syndrome;Molecular Genetics of Inherited Eye Disorders;1994-12

3. The Oculocerebrorenal Syndrome of Lowe;Advances in Pediatrics;1991

4. Urinary Glycosaminoglycans in Patients with Hypothyroidism and in Healthy Subjects;Clinical Chemistry and Laboratory Medicine;1988

5. Decreased procollagen production in cultured fibroblasts from patients with Lowe's syndrome;Journal of Inherited Metabolic Disease;1985-12

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