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Scandinavian Journal of Clinical and Laboratory Investigation Volume 38, 1978 - Issue sup150
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Original

Erythrocyte Membrane Alterations in Lecithin: Cholesterol Acyltransferase Deficiency

D. V. Godin Departments of Pharmacology and Pathology, University of British Columbia, Vancouver, Canada
,
G. R. Gray Departments of Pharmacology and Pathology, University of British Columbia, Vancouver, Canada
&
J. Frohlich Departments of Pharmacology and Pathology, University of British Columbia, Vancouver, Canada
Pages 162-167 | Published online: 14 Feb 2011

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G. Arienti, E. Carlini, L. Scionti, E. Puxeddu & P. Brunetti. (1995) Liver Alcoholic Cirrhosis and Spur-Cell (Acanthocytic) Anaemia: A Study of Erythrocyte Ghost Composition and Fluidity. Scandinavian Journal of Gastroenterology 30:12, pages 1204-1209.
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J. Frohlich, W. J. Godolphin, C. E. Reeve & K. A. Evelyn. (1978) Familial LCAT Deficiency Report of Two Patients from a Canadian Family of Italian and Swedish Descent. Scandinavian Journal of Clinical and Laboratory Investigation 38:sup150, pages 156-161.
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Articles from other publishers (9)

Xuechun Bai, Tianfu Yang, Austin M. Putz, Zhiquan Wang, Changxi Li, Frédéric Fortin, John C. S. Harding, Michael K. Dyck, Jack C. M. Dekkers, Catherine J. Field & Graham S. Plastow. (2021) Investigating the genetic architecture of disease resilience in pigs by genome-wide association studies of complete blood count traits collected from a natural disease challenge model. BMC Genomics 22:1.
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Masayuki Kuroda, Hideaki Bujo, Koutaro Yokote, Takeyoshi Murano, Takashi Yamaguchi, Masatsune Ogura, Katsunori Ikewaki, Masahiro Koseki, Yasuo Takeuchi, Atsuko Nakatsuka, Mika Hori, Kota Matsuki, Takashi Miida, Shinji Yokoyama, Jun Wada & Mariko Harada-Shiba. (2021) Current Status of Familial LCAT Deficiency in Japan. Journal of Atherosclerosis and Thrombosis 28:7, pages 679-691.
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Gilles Lambert, Naohiko Sakai, Boris L. Vaisman, Edward B. Neufeld, Benoit Marteyn, Chi-Chao Chan, Beverly Paigen, Enrico Lupia, Alton Thomas, Liliane J. Striker, Joan Blanchette-Mackie, Gyorgy Csako, John N. Brady, Rene Costello, Gary E. Striker, Alan T. Remaley, H. Bryan BrewerJr.Jr. & Silvia Santamarina-Fojo. (2001) Analysis of Glomerulosclerosis and Atherosclerosis in Lecithin Cholesterol Acyltransferase-deficient Mice. Journal of Biological Chemistry 276:18, pages 15090-15098.
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Shiro JimiNoriko UesugiKeijiro SakuHiroyuki ItabeBo ZhangKikuo ArakawaShigeo Takebayashi. (1999) Possible Induction of Renal Dysfunction in Patients With Lecithin:Cholesterol Acyltransferase Deficiency by Oxidized Phosphatidylcholine in Glomeruli. Arteriosclerosis, Thrombosis, and Vascular Biology 19:3, pages 794-801.
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H.E. MiettinenH. GyllingJ. TenhunenJ. VirtamoM. JauhiainenJ.K. HuttunenI. KantolaT.A. MiettinenK. Kontula. (1998) Molecular Genetic Study of Finns With Hypoalphalipoproteinemia and Hyperalphalipoproteinemia. Arteriosclerosis, Thrombosis, and Vascular Biology 18:4, pages 591-598.
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H. MiettinenH. GyllingI. UlmanenT. A. MiettinenK. Kontula. (1995) Two Different Allelic Mutations in a Finnish Family With Lecithin:Cholesterol Acyltransferase Deficiency. Arteriosclerosis, Thrombosis, and Vascular Biology 15:4, pages 460-467.
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N. BIZZARO, I. PIAZZA, G. BALDO & A. BARITUSSIO. (2008) Alcohol induced burr cell (echinocytic) haemolytic anaemia and haemochromatosis. Clinical & Laboratory Haematology 15:2, pages 93-102.
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Bernard Cantin, Louis-Daniel Brun, Claude Gagné, M.R.Ven Murthy, Paul-J. Lupien & Pierre Julien. (1992) Alterations in erythrocyte membrane lipid composition and fluidity in primary lipoprotein lipase deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease 1139:1-2, pages 25-31.
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A F Winder, A Garner, G A Sheraidah & P Barry. (1985) Familial lecithin:cholesterol acyltransferase deficiency. Biochemistry of the cornea.. Journal of Lipid Research 26:3, pages 283-287.
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