BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

211 related articles for article (PubMed ID: 1630033)

  • 1. [A case of familial lecithin: cholesterol acyltransferase deficiency].
    Baba Y; Hamada F; Aozaki S; Hagihara R; Ohashi T; Yasumoto Y; Ohsaki K; Yamashita W; Harada R; Arima T
    Nihon Jinzo Gakkai Shi; 1992 Mar; 34(3):309-16. PubMed ID: 1630033
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Membrane cholesterol and insulin receptor in erythrocytes].
    Maehara K
    Fukuoka Igaku Zasshi; 1991 Nov; 82(11):586-602. PubMed ID: 1774014
    [TBL] [Abstract][Full Text] [Related]  

  • 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
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 18(1):132. PubMed ID: 31164121
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Renal failure in familial lecithin: cholesterol acyltransferase deficiency.
    Borysiewicz LK; Soutar AK; Evans DJ; Thompson GR; Rees AJ
    Q J Med; 1982; 51(204):411-26. PubMed ID: 7156322
    [TBL] [Abstract][Full Text] [Related]  

  • 7. LCAT deficiency: molecular and phenotypic characterization of an Italian family.
    Gigante M; Ranieri E; Cerullo G; Calabresi L; Iolascon A; Assmann G; Morrone L; Pisciotta L; Schena FP; Gesualdo L
    J Nephrol; 2006; 19(3):375-81. PubMed ID: 16874701
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Compound heterozygosity (G71R/R140H) in the lecithin:cholesterol acyltransferase (LCAT) gene results in an intermediate phenotype between LCAT-deficiency and fish-eye disease.
    Hörl G; Kroisel PM; Wagner E; Tiran B; Petek E; Steyrer E
    Atherosclerosis; 2006 Jul; 187(1):101-9. PubMed ID: 16216249
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Familial lecithin-cholesterol acyltransferase deficiency.
    Jahanzad I; Amoueian S; Attaranzadeh A
    Arch Iran Med; 2009 Mar; 12(2):179-81. PubMed ID: 19249891
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 212(4):225-32. PubMed ID: 7148518
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 99(6):816-26. PubMed ID: 7077125
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 228(1):193-7. PubMed ID: 23522979
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Spin label studies of erythrocytes with abnormal lipid composition: comparison of red cells in a hereditary hemolytic syndrome and lecithin: cholesterol acyltransferase deficiency.
    Godin DV; Herring FG
    J Supramol Struct Cell Biochem; 1981; 15(3):213-8. PubMed ID: 6267314
    [TBL] [Abstract][Full Text] [Related]  

  • 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; 74(4):510-522. PubMed ID: 31103331
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Point mutation (C to T) of the LCAT gene resulting in A140C substitution.
    Hirashio S; Izumi K; Ueno T; Arakawa T; Naito T; Taguchi T; Yorioka N
    J Atheroscler Thromb; 2010 Dec; 17(12):1297-301. PubMed ID: 20938102
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Familial LCAT deficiency--clinical picture. Case report].
    Idzior-Waluś B; Sieradzki J; Rostworowski W; Hartwich J; Kaczmarski F; Dubiel-Bigaj M; Dabroś W
    Pol Arch Med Wewn; 2000 Sep; 104(3):591-6. PubMed ID: 11392166
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Study of erythrocytes in a hereditary hemolytic syndrome (HHS): comparison with erythrocytes in lecithin:cholesterol acyltransferase (LCAT) deficiency.
    Godin DV; Gray GR; Frohlich J
    Scand J Haematol; 1980 Feb; 24(2):122-30. PubMed ID: 6246569
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Splenomegaly with sea-blue histiocytosis, dyslipidemia, and nephropathy in a patient with lecithin-cholesterol acyltransferase deficiency: a clinicopathologic correlation.
    Naghashpour M; Cualing H
    Metabolism; 2009 Oct; 58(10):1459-64. PubMed ID: 19592052
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hypocomplementemic type II membranoproliferative glomerulonephritis in a male patient with familial lecithin-cholesterol acyltransferase deficiency due to two different allelic mutations.
    Sessa A; Battini G; Meroni M; Daidone G; Carnera I; Brambilla PL; Viganò G; Giordano F; Pallotti F; Torri Tarelli L; Calabresi L; Rolleri M; Bertolini S
    Nephron; 2001 Jul; 88(3):268-72. PubMed ID: 11423760
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Proteinuria in early childhood due to familial LCAT deficiency caused by loss of a disulfide bond in lecithin:cholesterol acyl transferase.
    Holleboom AG; Kuivenhoven JA; van Olden CC; Peter J; Schimmel AW; Levels JH; Valentijn RM; Vos P; Defesche JC; Kastelein JJ; Hovingh GK; Stroes ES; Hollak CE
    Atherosclerosis; 2011 May; 216(1):161-5. PubMed ID: 21315357
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 11.