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Original Article

Familial Lecithin: Cholesterol Acyltransferase Deficiency: Report of a Third Norwegian Family with Two Afflicted Members

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Pages 101-105 | Published online: 28 Aug 2009

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S. Chapelle, C. Franclois & J. M. Chantraine. (1982) Abnormalities of erythrocyte stromal lipids in atresia of the intrahepatic bile ducts. Archives Internationales de Physiologie et de Biochimie 90:1, pages 35-48.
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C. Naito, T. Teramoto, H. Kato, T. Watanabe, T. Yamanaka & A. Iwamoto. (1978) Lipid Compositions of Plasma Major Lipoproteins and Lipoprotein Lipase Activity in Hypolipidemic and Hyperlipidemic Siblings with Familial LCAT Deficiency. Scandinavian Journal of Clinical and Laboratory Investigation 38:sup150, pages 168-176.
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Ståle Ritland. (1975) The Abnormal ‘Lipoprotein of Cholestasis’, Lipoprotein-X. Scandinavian Journal of Gastroenterology 10:8, pages 785-789.
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John A. Glomset, Kaare R. Norum, Alex V. Nichols, Weiling C. King, Carolyn D. Mitchell, Kenneth R. Applegate, Elaine L. Gong & Egil Gjone. (1975) Plasma Lipoproteins in Familial Lecithin:Cholesterol Acyltransferase Deficiency: Effects of Dietary Manipulation. Scandinavian Journal of Clinical and Laboratory Investigation 35:sup142, pages 3-30.
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T. Hovig & E. Gjone. (1974) Familial Lecithin: Cholesterol Acyltransferase Deficiency: Ultrastructural Studies on Lipid Deposition and Tissue Reactions. Scandinavian Journal of Clinical and Laboratory Investigation 33:sup137, pages 135-146.
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Egil Gjone. (1974) Familial Lecithin: Cholesterol Acyltransferase Deficiency — A Clinical Survey. Scandinavian Journal of Clinical and Laboratory Investigation 33:sup137, pages 73-82.
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Kaare R. Norum & Egil Gjone. (1974) Editorial: Lecithin: Cholesterol Acyltransferase Recent Research on Biochemistry and Physiology of the Enzyme. Scandinavian Journal of Clinical and Laboratory Investigation 33:3, pages 191-197.
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Articles from other publishers (9)

Erwin Garcia, Irina Shalaurova, Steven P. Matyus, Lita A. Freeman, Edward B. Neufeld, Maureen L. Sampson, Rafael Zubirán, Anna Wolska, Alan T. Remaley, James D. Otvos & Margery A. Connelly. (2024) A High-Throughput NMR Method for Lipoprotein-X Quantification. Molecules 29:3, pages 564.
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Edward G. Lynn, Yaw L. Siow, Jiri Frohlich, Giselle T.Y. Cheung & O. Karmin. (2001) Lipoprotein-X stimulates monocyte chemoattractant protein-1 expression in mesangial cells via nuclear factor-κB. Kidney International 60:2, pages 520-532.
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J A Kuivenhoven, H Pritchard, J Hill, J Frohlich, G Assmann & J Kastelein. (1997) The molecular pathology of lecithin:cholesterol acyltransferase (LCAT) deficiency syndromes. Journal of Lipid Research 38:2, pages 191-205.
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H G Klein, P Lohse, N Duverger, J J Albers, D J Rader, L A Zech, S Santamarina-Fojo & HB BrewerJrJr. (1993) Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83–>stop) and LCAT (tyr156–>asn).. Journal of Lipid Research 34:1, pages 49-58.
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Grethe Skretting, Jan P. Blomhoff, Jorun Solheim & Hans Prydz. (2001) The genetic defect of the original Norwegian lecithin:cholesterol acyltransferase deficiency families. FEBS Letters 309:3, pages 307-310.
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Stanley Meizel. (2005) Molecules that initiate or help stimulate the acrosome reaction by their interaction with the mammalian sperm surface. American Journal of Anatomy 174:3, pages 285-302.
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C Chen, K Applegate, W C King, J A Glomset, K R Norum & E Gjone. (1984) A study of the small spherical high density lipoproteins of patients afflicted with familial lecithin: cholesterol acyltransferase deficiency.. Journal of Lipid Research 25:3, pages 269-282.
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J A Glomset, K Applegate, T Forte, W C King, C D Mitchell, K R Norum & E Gjone. (1980) Abnormalities in lipoproteins of d < 1.006 g/ml in familial lecithin:cholesterol acyltransferase deficiency. Journal of Lipid Research 21:8, pages 1116-1127.
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A. Weizel & M. Liersch. 1976. Fettstoffwechsel. Fettstoffwechsel 37 96 .

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