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Journal Abstract Search

204 related items for PubMed ID: 91022

  • 1. Fish-eye disease. A new familial condition with massive corneal opacities and dyslipoproteinaemia.
    Carlson LA, Philipson B.
    Lancet; 1979 Nov 03; 2(8149):922-4. PubMed ID: 91022
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  • 3. Fish-eye disease: Another under-recognized cause of familial corneal opacification.
    Kapoor S.
    Ophthalmic Genet; 2016 Sep 03; 37(3):349. PubMed ID: 26854387
    [No Abstract] [Full Text] [Related]

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  • 5. Cholesteryl ester transfer activity in plasma of patients with familial high-density lipoprotein deficiency.
    Sparks DL, Frohlich J, Pritchard PH.
    Clin Chem; 1988 Sep 03; 34(9):1812-5. PubMed ID: 3416429
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  • 6. In vitro normalization of cholesteryl ester content and particle size of fish eye disease high density lipoproteins.
    Holmquist L, Carlson LA.
    Acta Med Scand; 1987 Sep 03; 221(3):283-9. PubMed ID: 3591466
    [Abstract] [Full Text] [Related]

  • 7. 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 Sep 03; 222(4):345-50. PubMed ID: 3425387
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  • 8. Lecithin:cholesterol acyltransferase activity in relation to lipoprotein concentration and lipid composition.
    Leiss O, Murawski U, Egge H.
    Scand J Clin Lab Invest Suppl; 1978 Sep 03; 150():77-84. PubMed ID: 218279
    [No Abstract] [Full Text] [Related]

  • 9. 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 Sep 03; 218(2):189-96. PubMed ID: 4061122
    [Abstract] [Full Text] [Related]

  • 10. The role of high density lipoproteins in lecithin:cholesterol acyltransferase activity: perspectives from Tangier disease.
    Assmann G, Schmitz G, Heckers H.
    Scand J Clin Lab Invest Suppl; 1978 Sep 03; 150():98-102. PubMed ID: 218282
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  • 11. The molecular basis of lecithin:cholesterol acyltransferase deficiency syndromes: a comprehensive study of molecular and biochemical findings in 13 unrelated Italian families.
    Calabresi L, Pisciotta L, Costantin A, Frigerio I, Eberini I, Alessandrini P, Arca M, Bon GB, Boscutti G, Busnach G, Frascà G, Gesualdo L, Gigante M, Lupattelli G, Montali A, Pizzolitto S, Rabbone I, Rolleri M, Ruotolo G, Sampietro T, Sessa A, Vaudo G, Cantafora A, Veglia F, Calandra S, Bertolini S, Franceschini G.
    Arterioscler Thromb Vasc Biol; 2005 Sep 03; 25(9):1972-8. PubMed ID: 15994445
    [Abstract] [Full Text] [Related]

  • 12. A kindred with fish eye disease, corneal opacities, marked high-density lipoprotein deficiency, and statin therapy.
    Dimick SM, Sallee B, Asztalos BF, Pritchard PH, Frohlich J, Schaefer EJ.
    J Clin Lipidol; 2014 Sep 03; 8(2):223-30. PubMed ID: 24636183
    [Abstract] [Full Text] [Related]

  • 13. Two different allelic mutations in the lecithin-cholesterol acyltransferase gene associated with the fish eye syndrome. Lecithin-cholesterol acyltransferase (Thr123----Ile) and lecithin-cholesterol acyltransferase (Thr347----Met).
    Klein HG, Lohse P, Pritchard PH, Bojanovski D, Schmidt H, Brewer HB.
    J Clin Invest; 1992 Feb 03; 89(2):499-506. PubMed ID: 1737840
    [Abstract] [Full Text] [Related]

  • 14. Plasma lipid transfer in fish-eye disease.
    Calvert GD, Carlson LA.
    Acta Med Scand; 1983 Feb 03; 213(4):253-4. PubMed ID: 6613682
    [Abstract] [Full Text] [Related]

  • 15. Plasma lecithin:cholesterol acyltransferase activity in hypophysectomized rats.
    Manninen V, Mälkönen M, Blomhoff JP, Gjone E.
    Scand J Clin Lab Invest Suppl; 1978 Feb 03; 150():147-50. PubMed ID: 218273
    [Abstract] [Full Text] [Related]

  • 16. Biochemical studies in a patient with a Tangier syndrome.
    Yao JK, Herbert PN, Fredrickson DS, Ellefson RD, Heinen RJ, Forte T, Dyck PJ.
    J Neuropathol Exp Neurol; 1978 Feb 03; 37(2):138-54. PubMed ID: 632844
    [Abstract] [Full Text] [Related]

  • 17. Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from northwestern Norway.
    Gjone E, Blomhoff JP, Holme R, Hovig T, Olaisen B, Skarbøvik AJ, Teisberg P.
    Acta Med Scand; 1981 Feb 03; 210(1-2):3-6. PubMed ID: 7293825
    [Abstract] [Full Text] [Related]

  • 18. Abnormal plasma lipoproteins and lecithin-cholesterol acyltransferase deficiency in alcoholic liver disease.
    Sabesin SM, Hawkins HL, Kuiken L, Ragland JB.
    Gastroenterology; 1977 Mar 03; 72(3):510-8. PubMed ID: 188710
    [Abstract] [Full Text] [Related]

  • 19. Hypoalphalipoproteinemia resembling fish eye disease.
    Frohlich J, Hoag G, McLeod R, Hayden M, Godin DV, Wadsworth LD, Critchley JD, Pritchard PH.
    Acta Med Scand; 1987 Mar 03; 221(3):291-8. PubMed ID: 3591467
    [Abstract] [Full Text] [Related]

  • 20. A first British case of fish-eye disease presenting at age 75 years: a double heterozygote for defined and new mutations affecting LCAT structure and expression.
    Winder AF, Owen JS, Pritchard PH, Lloyd-Jones D, Vallance DT, White P, Wray R.
    J Clin Pathol; 1999 Mar 03; 52(3):228-30. PubMed ID: 10450185
    [Abstract] [Full Text] [Related]

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