Skip to main content

. 1947;41(3):438–449.

Studies on alcaptonuria

2. Investigations on a case of human alcaptonuria

A Neuberger ¹, C Rimington ¹, J M G Wilson ¹

PMCID: PMC1258507 PMID: 16748189

445

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

Levine S. Z., Marples E., Gordon H. H. A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. I. IDENTIFICATION AND ASSAY OF INTERMEDIARY PRODUCTS. J Clin Invest. 1941 Mar;20(2):199–207. doi: 10.1172/JCI101212. [DOI] [PMC free article] [PubMed] [Google Scholar]
Medes G. A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine. Biochem J. 1932;26(4):917–940. doi: 10.1042/bj0260917. [DOI] [PMC free article] [PubMed] [Google Scholar]
Neuberger A. Studies on alcaptonuria: 1. The estimation of homogentisic acid. Biochem J. 1947;41(3):431–438. doi: 10.1042/bj0410431. [DOI] [PMC free article] [PubMed] [Google Scholar]
Neuberger A., Webster T. A. Studies in alcaptonuria: 3. Experimental alcaptonuria in rats. Biochem J. 1947;41(3):449–457. [PMC free article] [PubMed] [Google Scholar]
Penrose L., Quastel J. H. Metabolic studies in phenylketonuria. Biochem J. 1937 Feb;31(2):266–274. doi: 10.1042/bj0310266. [DOI] [PMC free article] [PubMed] [Google Scholar]

ACTIONS

PDF (2.2 MB)

RESOURCES