EVALUATION OF THE NITROPRUSSIDE TEST FOR THE DIAGNOSIS OF CYSTINURIA

Author:

Smith Arabella1

Affiliation:

1. Oliver Latham Laboratory, New South Wales Health Commission

Publisher

AMPCo

Subject

General Medicine

Reference16 articles.

1. Amino Acid Metabolism, Volume 10: Major Problems in Clinical Paediatrics;Scriver C. R.;Saunders, Philadelphia, London, Toronto,1973

2. Metabolic Basis of Inherited Disease;Stanbury J. B.;3rd Edition, McGraw Hill Book Company,1972

3. The occurrence of cystinuria in healthy young men and women;Lewis H. B.;Ann. intern. Med.,1932

4. Cystinuria

5. The incidence of homozygous cystinuria in Swedish school children;Bostrom H.;Acta. paediat. (Uppsala),1959

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1. Cystinuria in a 13-month-old girl with absence of mutations in the SLC3A1 and SLC7A9 Genes;Indian Journal of Nephrology;2018

2. Etiology of Urolithiasis;Urolithiasis in Clinical Practice;2017

3. Cystinuria Associated with Different SLC7A9 Gene Variants in the Cat;PLOS ONE;2016-07-12

4. CKD and Its Risk Factors among Patients with Cystinuria;Clinical Journal of the American Society of Nephrology;2015-02-25

5. Evaluation and Medical Management of Urinary Lithiasis;Campbell-Walsh Urology;2012

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