Familial high-density lipoprotein deficiency (Tangier disease): the third Italian case.

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作者信息

Bracco G, Dotti G, Levis F, David E, Saracco G, Rizzetto M, Verme G

机构信息

Laboratorio Analisi chimico-cliniche, Ospedale Infantile Regina Margherita, Torino, Italy.

出版信息

J Inherit Metab Dis. 1988;11 Suppl 2:155-7. doi: 10.1007/BF01804223.

DOI:10.1007/BF01804223

PMID:3141697

Abstract

摘要

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Familial high-density lipoprotein deficiency (Tangier disease): the third Italian case.

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Aortic features in Tangier disease and pathogenetic considerations--Part I. Fatty dots and streaks.Tangier病的主动脉特征及发病机制探讨——第一部分。脂肪点和条纹。

Eur J Epidemiol. 1992 May;8 Suppl 1:36-47. doi: 10.1007/BF00145348.

本文引用的文献

Neuropathy in Tangier disease: A clinicopathologic study and a review of the literature.

Acta Neurol Scand. 1985 Nov;72(5):495-505. doi: 10.1111/j.1600-0404.1985.tb00907.x.

Plasma apolipoproteins in Tangier disease, as studied with two-dimensional electrophoresis.用二维电泳法研究丹吉尔病中的血浆载脂蛋白。

Clin Chem. 1987 Jan;33(1):120-2.

Immunochemical study of the plasma low and high density lipoproteins in Tangier disease.丹吉尔病患者血浆低密度和高密度脂蛋白的免疫化学研究

FEBS Lett. 1986 May 26;201(1):163-7. doi: 10.1016/0014-5793(86)80591-9.

Properties of the plasma very low and low density lipoproteins in Tangier disease.丹吉尔病中血浆极低密度脂蛋白和低密度脂蛋白的特性

J Clin Invest. 1978 Jan;61(1):120-32. doi: 10.1172/JCI108910.

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