Late Onset Diabetes Mellitus in Patients with Hereditary Aceruloplasminemia.

MIYAJIMA H; TAKAHASHI Y; SHIMIZU H; SAKAI N; KAMATA T; KANEKO E

Art

J-GLOBAL ID：200902173285191452 Reference number：96A0929946

Late Onset Diabetes Mellitus in Patients with Hereditary Aceruloplasminemia.

遺伝性セルロプラスミン欠乏症を持つ患者における晩期発生糖尿病

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Material：
Volume： 35 Issue： 8 Page： 641-645 Publication year： Aug. 1996
JST Material Number： Z0157B ISSN： 0918-2918 Document type： Article
Article type：短報 Country of issue： Japan (JPN) Language： ENGLISH (EN)

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Metabolic diseases,nutritional diseases in general.

Reference (19)：

1) Miyajima H, Nishimura Y, Mizoguchi K, Sakamoto M, Shimizu T, Honda N. Familial apoceruloplasmin deficiency associated with blepharospasm and retinal degeneration. Neurology 37: 761, 1987.
3) Morita H, Ikeda S, Yamamoto K, et al. Hereditary ceruloplasmin deficiency with hemosiderosis: A clinicopathological study of a Japanese family. Ann Neurol 37: 646, 1995.
4) Harris ZL, Takahashi Y, Miyajima H, Serizawa M, MacGillivray RTA, Gitlin ID. Aceruloplasminemia: molecular characterization of this disorder of iron metabolism. Proc Natl Acad Sci USA 92: 2539, 1995.
5) Yoshida K, Furihata K, Takeda S, et al. A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans. Nat Genet 9: 267, 1995.
6) Daimon M, Kato T, Kawanami T, et al. A nonsense mutation of the ceruloplasmin gene in hereditary ceruloplasmin deficiency with diabetes mellitus. Biochem Biophys Res Commun 217: 89, 1995.

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