Similar articles

• Decreased xanthine oxidase activities and increased urinary oxypurines in heterozygotes for hereditary xanthinuria.

  Kawachi M, Kono N, Mineo I, Yamada Y, Tarui S. Kawachi M, et al. Clin Chim Acta. 1990 Apr 30;188(2):137-46. doi: 10.1016/0009-8981(90)90158-o. Clin Chim Acta. 1990. PMID: 2379312
• Asymptomatic hereditary xanthinuria: a case report.

  Nagae A, Murakami E, Hiwada K, Sato Y, Kawachi M, Kono N. Nagae A, et al. Jpn J Med. 1990 May-Jun;29(3):287-91. doi: 10.2169/internalmedicine1962.29.287. Jpn J Med. 1990. PMID: 2273608 Review.
• A xanthinuric family--the proposita having immunologically reactive xanthine oxidase but no xanthine oxidase activity.

  Yamamoto T, Moriwaki Y, Takahashi S, Hada T, Suda M, Imanishi H, Agbedana OE, Nanahoshi M, Higashino K. Yamamoto T, et al. Adv Exp Med Biol. 1991;309A:369-72. doi: 10.1007/978-1-4899-2638-8_84. Adv Exp Med Biol. 1991. PMID: 1789246
• A case of xanthinuria: a study on the metabolism of pyrazinamide and allopurinol.

  Yamamoto T, Kario K, Suda M, Moriwaki Y, Takahashi S, Higashino K. Yamamoto T, et al. Jpn J Med. 1991 Sep-Oct;30(5):430-4. doi: 10.2169/internalmedicine1962.30.430. Jpn J Med. 1991. PMID: 1803043
• [Xanthine oxidase deficiency (hereditary xanthinuria), molybdenum cofactor deficiency].

  Sumi S, Wada Y. Sumi S, et al. Nihon Rinsho. 1996 Dec;54(12):3333-6. Nihon Rinsho. 1996. PMID: 8976115 Review. Japanese.