These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. RENAL TUBULAR TRANSPORT OF PROLINE, HYDROXYPROLINE, AND GLYCINE IN HEALTH AND IN FAMILIAL HYPERPROLINEMIA. SCRIVER CR, EFRON ML, SCHAFER IA. J Clin Invest; 1964 Mar 27; 43(3):374-85. PubMed ID: 14135488 [No Abstract] [Full Text] [Related]
4. DISORDERS OF AMINO ACID TRANSPORT. SEGAL S. Ann Intern Med; 1965 Apr 27; 62():847-51. PubMed ID: 14274849 [No Abstract] [Full Text] [Related]
8. AN INBORN ERROR OF METABOLISM ASSOCIATED WITH DEFICIENCY OF ENZYME CYSTATHIONINE SYNTHETASE LEADING TO HOMOCYSTINURIA. WRIGHT LD. N Y State J Med; 1965 Feb 15; 65():559-61. PubMed ID: 14276302 [No Abstract] [Full Text] [Related]
12. ADAPTATION OF MONODIRECTIONAL HIGH-VOLTAGE ELECTROPHORESIS ON LONG PAPERS TO THE RAPID QUALITATIVE IDENTIFICATION OF URINARY AMINO ACIDS. SACKETT DL. J Lab Clin Med; 1964 Feb 15; 63():306-14. PubMed ID: 14125118 [No Abstract] [Full Text] [Related]
13. CYSTINURIA IN SWEDEN. X. QUANTITATIVE STUDIES ON THE URINARY AMINO ACID EXCRETION IN CYSTINURICS. HAMBRAEUS L. Acta Soc Med Ups; 1964 Feb 15; 69():1-22. PubMed ID: 14136265 [No Abstract] [Full Text] [Related]
16. [Physiological and pathological aminoacidurias]. Brodehl J. Monatsschr Kinderheilkd (1902); 1973 May 15; 121(5):190-200. PubMed ID: 4713389 [No Abstract] [Full Text] [Related]
17. MENTAL RETARDATION AND ABNORMAL AMINOACIDURIAS OCCURRING IN A FAMILY. ANYON CP. N Z Med J; 1965 Jan 15; 64():3-7. PubMed ID: 14259628 [No Abstract] [Full Text] [Related]
19. Protein intolerance with deficient transport of basic aminoacids. Another inborn error of metabolism. Perheentupa J, Visakorpi JK. Lancet; 1965 Oct 23; 2(7417):813-6. PubMed ID: 4158034 [No Abstract] [Full Text] [Related]
20. HOMOCYSTINURIA, AN ERROR IN THE METABOLISM OF METHIONINE. GERRITSEN T, WAISMAN HA. Pediatrics; 1964 Mar 23; 33():413-20. PubMed ID: 14129086 [No Abstract] [Full Text] [Related] Page: [Next] [New Search]