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

Familial LCAT Deficiency Report of Two Patients from a Canadian Family of Italian and Swedish Descent

J. Frohlich Departments of Pathology and Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada
, M.D.,
W. J. Godolphin Departments of Pathology and Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada
,
C. E. Reeve Departments of Pathology and Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada
&
K. A. Evelyn Departments of Pathology and Medicine, Vancouver General Hospital, University of British Columbia, Vancouver, BC, Canada
Pages 156-161 | Published online: 14 Feb 2011

Citations (12)

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Read on this site (2)

K. G. Varma, L. A. Soloff & J. Frohlich. (1978) Immunological Evaluation of LCAT Deficiency. Scandinavian Journal of Clinical and Laboratory Investigation 38:sup150, pages 6-11.
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D. V. Godin, G. R. Gray & J. Frohlich. (1978) Erythrocyte Membrane Alterations in Lecithin: Cholesterol Acyltransferase Deficiency. Scandinavian Journal of Clinical and Laboratory Investigation 38:sup150, pages 162-167.
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Articles from other publishers (10)

Cecilia Vitali, Archna Bajaj, Christina Nguyen, Jill Schnall, Jinbo Chen, Kostas Stylianou, Daniel J. Rader & Marina Cuchel. (2022) A systematic review of the natural history and biomarkers of primary lecithin:cholesterol acyltransferase deficiency. Journal of Lipid Research 63:3, pages 100169.
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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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K Moriyama, J Sasaki, F Arakawa, N Takami, E Maeda, A Matsunaga, Y Takada, K Midorikawa, T Yanase & G Yoshino. (1995) Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344–>Ser). Journal of Lipid Research 36:11, pages 2329-2343.
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T OhtaS HattoriR NakamuraS HoriuchiJ FrohlichK TakataY IkedaY SaitoI Matsuda. (1994) Characterization of subspecies of apolipoprotein A-I-containing lipoprotein in homozygotes for familial lecithin:cholesterol acyltransferase deficiency.. Arteriosclerosis and Thrombosis: A Journal of Vascular Biology 14:7, pages 1137-1145.
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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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Y I Parmar, D L Sparks, J Frohlich, P R Cullis & P H Pritchard. (1989) Detection of vesicular lipoproteins in lecithin:cholesterol acyltransferase-deficient plasma by 1H-NMR spectroscopy.. Journal of Lipid Research 30:5, pages 765-771.
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J T Buckley, R McLeod & J Frohlich. (1984) Action of a microbial glycerophospholipid:cholesterol acyltransferase on plasma from normal and LCAT-deficient subjects.. Journal of Lipid Research 25:9, pages 913-918.
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Roger McLeod, C. Edward Reeve & Jiri Frohlich. (1984) Plasma lipoproteins and lecithin:cholesterol acyltransferase distribution in patients on dialysis. Kidney International 25:4, pages 683-688.
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C H Chen & J J Albers. (1982) Characterization of proteoliposomes containing apoprotein A-I: a new substrate for the measurement of lecithin: cholesterol acyltransferase activity.. Journal of Lipid Research 23:5, pages 680-691.
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