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Sulfur amino acid metabolism in cystinuria: A biochemical and clinical study of patients

✍ Scribed by Mårtensson, Johannes; Denneberg, Torsten; Lindell, Åke; Textorius, Ola

Book ID
109881549
Publisher
Nature Publishing Group
Year
1990
Tongue
English
Weight
732 KB
Volume
37
Category
Article
ISSN
0085-2538

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Biochemical and clinical studies in Liby
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✍ Pras, Elon; Kochba, Ilan; Lubetzky, Aharon; Pras, Mordechai; Sidi, Yechezkel; Ka 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 16 KB 👁 2 views

Cystinuria is a hereditary disorder manifested by the development of kidney stones. Three subtypes of the disease have been described, based on urinary excretion of cystine and the dibasic amino acids in heterozygotes, and oral loading tests in homozygotes. Cystinuria is very common among Libyan Jew