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Journal Abstract Search

237 related items for PubMed ID: 3141686

  • 1. Familial LCAT deficiency and fish-eye disease.
    McIntyre N.
    J Inherit Metab Dis; 1988; 11 Suppl 1():45-56. PubMed ID: 3141686
    [Abstract] [Full Text] [Related]

  • 2. Evidence for deficiency of high density lipoprotein lecithin: cholesterol acyltransferase activity (alpha-LCAT) in fish eye disease.
    Carlson LA, Holmquist L.
    Acta Med Scand; 1985; 218(2):189-96. PubMed ID: 4061122
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  • 3. [Familial LCAT deficiency].
    Kinoshita M.
    Nihon Rinsho; 1994 Dec; 52(12):3210-5. PubMed ID: 7853712
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  • 5. Alpha-lecithin:cholesterol acyltransferase deficiency. Lack of both phospholipase A2 and acyltransferase activities characteristic of high density lipoprotein lecithin:cholesterol acyltransferase in fish eye disease.
    Holmquist L, Carlson LA.
    Acta Med Scand; 1987 Dec; 222(1):23-6. PubMed ID: 3630775
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  • 6. Familial lecithin: cholesterol acyltransferase (LCAT) deficiency. An updated review Spring 1988.
    Gjone E.
    Ophthalmic Paediatr Genet; 1988 Nov; 9(3):167-9. PubMed ID: 3068599
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  • 7. Familial high-density-lipoprotein deficiency causing corneal opacities (fish eye disease) in a family of Dutch descent.
    Kastelein JJ, Pritchard PH, Erkelens DW, Kuivenhoven JA, Albers JJ, Frohlich JJ.
    J Intern Med; 1992 Apr; 231(4):413-9. PubMed ID: 1588268
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  • 8. Inhibitory effect of normal high density lipoproteins on lecithin:cholesterol acyltransferase activity in fish eye disease plasma.
    Holmquist L, Carlson LA.
    Acta Med Scand; 1987 Apr; 222(1):15-21. PubMed ID: 3630774
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  • 9. [Lecithin: cholesterol acyltransferase (LCAT)--the genetic analysis of familial LCAT deficiency and fish eye disease].
    Bujo H, Saito Y.
    Nihon Rinsho; 1995 May; 53(5):1260-6. PubMed ID: 7602789
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  • 10. Current Status of Familial LCAT Deficiency in Japan.
    Kuroda M, Bujo H, Yokote K, Murano T, Yamaguchi T, Ogura M, Ikewaki K, Koseki M, Takeuchi Y, Nakatsuka A, Hori M, Matsuki K, Miida T, Yokoyama S, Wada J, Harada-Shiba M.
    J Atheroscler Thromb; 2021 Jul 01; 28(7):679-691. PubMed ID: 33867422
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  • 11. Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
    Borysiewicz LK, Soutar AK, Evans DJ, Thompson GR, Rees AJ.
    Q J Med; 1982 Jul 01; 51(204):411-26. PubMed ID: 7156322
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  • 13. Different substrate specificities of plasma lecithin: cholesterol acyl transferase in fish eye disease and Tangier disease.
    Carlson LA, Holmquist L, Assmann G.
    Acta Med Scand; 1987 Jul 01; 222(4):345-50. PubMed ID: 3425387
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  • 14. Study of the components of reverse cholesterol transport in lecithin:cholesterol acyltransferase deficiency.
    Park MS, Kudchodkar BJ, Frohlich J, Pritchard H, Lacko AG.
    Arch Biochem Biophys; 1987 Nov 01; 258(2):545-54. PubMed ID: 3674887
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  • 15. Fish eye syndrome: a molecular defect in the lecithin-cholesterol acyltransferase (LCAT) gene associated with normal alpha-LCAT-specific activity. Implications for classification and prognosis.
    Klein HG, Santamarina-Fojo S, Duverger N, Clerc M, Dumon MF, Albers JJ, Marcovina S, Brewer HB.
    J Clin Invest; 1993 Jul 01; 92(1):479-85. PubMed ID: 8326012
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  • 17. Identification and functional analysis of missense mutations in the lecithin cholesterol acyltransferase gene in a Chilean patient with hypoalphalipoproteinemia.
    Tobar HE, Cataldo LR, González T, Rodríguez R, Serrano V, Arteaga A, Álvarez-Mercado A, Lagos CF, Vicuña L, Miranda JP, Pereira A, Bravo C, Aguilera CM, Eyheramendy S, Uauy R, Martínez Á, Gil Á, Francone O, Rigotti A, Santos JL.
    Lipids Health Dis; 2019 Jun 05; 18(1):132. PubMed ID: 31164121
    [Abstract] [Full Text] [Related]

  • 18. Recombinant human LCAT normalizes plasma lipoprotein profile in LCAT deficiency.
    Simonelli S, Tinti C, Salvini L, Tinti L, Ossoli A, Vitali C, Sousa V, Orsini G, Nolli ML, Franceschini G, Calabresi L.
    Biologicals; 2013 Nov 05; 41(6):446-9. PubMed ID: 24140107
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