Urinary excretion of 4-hydroxyphenyllactic acids and related compounds in man, including a screening test for tyrosyluria-Reference-Cited by-同舟云学术

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Urinary excretion of 4-hydroxyphenyllactic acids and related compounds in man, including a screening test for tyrosyluria

Published:1968-12 Issue:3 Volume:2 Page:216-226
ISSN:0006-2944
Container-title:Biochemical Medicine
language:en
Short-container-title:Biochemical Medicine

Author:

Coward R.F.,Smith P.

Publisher

Elsevier BV

Subject

Biochemistry

Reference17 articles.

1. Urinary Phenols in Stress

2. Symposium on Tyrosinosis,1966

3. A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine

4. The Metabolic Basis of Inherited Disease;Ladu,1960

5. An inborn defect in the metabolism of tyrosine in infants on a normal diet

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2. N ‐acetyl‐ l ‐tyrosine is an intrinsic triggering factor of mitohormesis in stressed animals;EMBO reports;2020-03-02

3. Inborn Errors of Metabolism that Lead to Permanent Liver Injury;Zakim and Boyer's Hepatology;2012

4. Inborn Errors of Metabolism that Lead to Permanent Liver Injury;Zakim and Boyer's Hepatology;2006

5. The occurrence of hepatoma in the chronic form of hereditary tyrosinemia;The Journal of Pediatrics;1976-03

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