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Journal Abstract Search

210 related items for PubMed ID: 1630033

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  • 2. Alterations in erythrocyte membrane lipid and its fragility in a patient with familial lecithin:cholesterol acyltrasferase (LCAT) deficiency.
    Suda T, Akamatsu A, Nakaya Y, Masuda Y, Desaki J.
    J Med Invest; 2002 Aug; 49(3-4):147-55. PubMed ID: 12323004
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  • 3. [Membrane cholesterol and insulin receptor in erythrocytes].
    Maehara K.
    Fukuoka Igaku Zasshi; 1991 Nov; 82(11):586-602. PubMed ID: 1774014
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  • 4. Hereditary lecithin-cholesterol acyltransferase deficiency. Case report of a German patient.
    Weber P, Owen JS, Desai K, Clemens MR.
    Am J Clin Pathol; 1987 Oct; 88(4):510-6. PubMed ID: 3661502
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  • 5. 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
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  • 9. Familial lecithin-cholesterol acyltransferase deficiency.
    Jahanzad I, Amoueian S, Attaranzadeh A.
    Arch Iran Med; 2009 Mar 05; 12(2):179-81. PubMed ID: 19249891
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  • 10. Familial plasma lecithin: cholesterol acyltransferase deficiency. A new family with partial LCAT activity.
    Sakuma M, Akanuma Y, Kodama T, Yamada N, Murata S, Murase T, Itakura H, Kosaka K.
    Acta Med Scand; 1982 Mar 05; 212(4):225-32. PubMed ID: 7148518
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  • 11. Hereditary plasma lecithin-cholesterol acyl transferase deficiency: a heterozygous variant with erythrocyte membrane abnormalities.
    Jain SK, Mohandas N, Sensabaugh GF, Shojania AM, Shohet SB.
    J Lab Clin Med; 1982 Jun 05; 99(6):816-26. PubMed ID: 7077125
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  • 12. Amelioration of circulating lipoprotein profile and proteinuria in a patient with LCAT deficiency due to a novel mutation (Cys74Tyr) in the lid region of LCAT under a fat-restricted diet and ARB treatment.
    Naito S, Kamata M, Furuya M, Hayashi M, Kuroda M, Bujo H, Kamata K.
    Atherosclerosis; 2013 May 05; 228(1):193-7. PubMed ID: 23522979
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  • 14. The P274S Mutation of Lecithin-Cholesterol Acyltransferase (LCAT) and Its Clinical Manifestations in a Large Kindred.
    Fountoulakis N, Lioudaki E, Lygerou D, Dermitzaki EK, Papakitsou I, Kounali V, Holleboom AG, Stratigis S, Belogianni C, Syngelaki P, Stratakis S, Evangeliou A, Gakiopoulou H, Kuivenhoven JA, Wevers R, Dafnis E, Stylianou K.
    Am J Kidney Dis; 2019 Oct 05; 74(4):510-522. PubMed ID: 31103331
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