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Hyperuricemia and Cystinuria

descriptionPublicationkeyboard_double_arrow_right Part of book or chapter of book , Article 01 Jan 1980Publisher:Springer US

Authors: Giorcelli G; Marangella M; Vacha G; B. Fruttero; B. Malfi; M. Bruno; F. Linari;

doi: 10.1007/978-1-4615-9140-5_21

pmid: 7424625

Hyperuricemia and Cystinuria

- Summary
- Subjects
- Metrics

Abstract

Cystinuria is an inherited disorder of the tubular and jejunal mucosa transport of four amino acids:cys, lys, arg and ornithine (1–2). The association of cystinuria with other chronic diseases or metabolic disorders is not common. Therefore it seemed us usefull to present the association hyperuricemia and cystinuria in 7 out of 55 cystinic lithiasis patients.

Keywords

Adult, Cystinuria, Middle Aged, Uric Acid, Kidney Calculi, Reference Values, Creatinine, Cystine, Humans, Amino Acids, Aged

Impact byBIP!

	citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	5
	popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.	Average
	influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).	Average
	impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.	Average