These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

113 related articles for article (PubMed ID: 6320428)

  • 1. [Genetic hypolipoproteinemias].
    Bakir R; Chanu B; Rouffy J
    Sem Hop; 1983 Dec; 59(49):3456-60. PubMed ID: 6320428
    [TBL] [Abstract][Full Text] [Related]  

  • 2. [Genetic hypolipoproteinemia].
    Bakir R; Chanu B; Rouffy J
    Pathol Biol (Paris); 1983 Sep; 31(7):601-5. PubMed ID: 6355992
    [TBL] [Abstract][Full Text] [Related]  

  • 3. [Familial alpha lipoprotein deficiency. Tangier disease, familial hypoalphalipoproteinemia and familial deficiency of lecithin cholesterol acyltransferase deficiency].
    Dioguardi N; Vergani C
    Minerva Med; 1983 Mar; 74(12):585-94. PubMed ID: 6835549
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genetic disorders of high-density lipoprotein metabolism and atherosclerosis--what can we learn?
    Utermann G
    Eur J Clin Invest; 1982 Feb; 12(1):5-7. PubMed ID: 6802652
    [No Abstract]   [Full Text] [Related]  

  • 5. Corneal opacification and familial disorders affecting plasma high-density lipoprotein.
    Winder AF; Borysiewicz LK
    Birth Defects Orig Artic Ser; 1982; 18(6):433-40. PubMed ID: 7171769
    [No Abstract]   [Full Text] [Related]  

  • 6. 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; 210(1-2):3-6. PubMed ID: 7293825
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Lipoprotein abnormalities associated with a viral syndrome.
    Friedland ML; Herbert PN
    JAMA; 1982 Jul; 248(1):82. PubMed ID: 6283187
    [No Abstract]   [Full Text] [Related]  

  • 8. Familial lecithin cholesterol acyltransferase (LCAT) deficiency.
    Gjone E
    Birth Defects Orig Artic Ser; 1982; 18(6):423-31. PubMed ID: 7171768
    [No Abstract]   [Full Text] [Related]  

  • 9. [Practical value of the selective precipitation of LDL, LDL-phospholipids and the molar ratio of cholesterol to LDL-phospholipids in lecithin-cholesterol-acyltransferase deficiency].
    Alcindor LG; Aalam H; Piot MC
    Ann Biol Clin (Paris); 1983; 41(5):311-4. PubMed ID: 6666872
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Hereditary lecithin-cholesterol acyltransferase deficiency. Report of 2 new cases and review of the literature.
    Shojania AM; Jain SK; Shohet SB
    Clin Invest Med; 1983; 6(1):49-55. PubMed ID: 6831794
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Case of familial lecithin: cholesterol acyltransferase deficiency].
    Kato K; Murayama N; Fujita T; Asano Y; Hosoda S; Maesawa M; Sakamoto Y; Murase T; Akanuma Y
    Nihon Naika Gakkai Zasshi; 1983 Dec; 72(12):1774-82. PubMed ID: 6676434
    [No Abstract]   [Full Text] [Related]  

  • 12. [Gastroenterologic diagnosis of hypolipoproteinemias with special emphasis on Tangier disease].
    Gheorghiu T; Assmann G; Mies R; Schaefer HE
    Verh Dtsch Ges Inn Med; 1978; (84):1050-3. PubMed ID: 217188
    [No Abstract]   [Full Text] [Related]  

  • 13. Identification of lipoprotein families in a variant of human plasma apolipoprotein A deficiency.
    Gustafson A; McConathy WJ; Alaupovic P; Curry MD; Persson B
    Scand J Clin Lab Invest; 1979 Jun; 39(4):377-87. PubMed ID: 230573
    [No Abstract]   [Full Text] [Related]  

  • 14. [Familial lecithin cholesterol acyltransferase deficiencies].
    Kinoshita M; Teramoto T
    Nihon Rinsho; 1983 Aug; 41(8):1832-7. PubMed ID: 6632292
    [No Abstract]   [Full Text] [Related]  

  • 15. 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]  

  • 16. [Familial lecithin cholesterol acyltransferase deficiency].
    Itakura H
    Tanpakushitsu Kakusan Koso; 1988 Apr; 33(5):791-3. PubMed ID: 3270894
    [No Abstract]   [Full Text] [Related]  

  • 17. [Both the enzymatic defect and the localization of the genetic defect has been clarified in the metabolic disease lecithin cholesterol acetyltransferase deficiency].
    Hamnström B
    Lakartidningen; 1983 Jun; 80(24):2490-3. PubMed ID: 6888097
    [No Abstract]   [Full Text] [Related]  

  • 18. Familial lecithin:cholesterol acyltransferase deficiency. Further studies on plasma lipoproteins and plasma postheparin lipase activity of a patient with normal renal function.
    Blomhoff JP; Holme R; Sauar J; Gjone E
    Scand J Clin Lab Invest Suppl; 1978; 150():177-82. PubMed ID: 218275
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual.
    Shojania AM; McAlpine PJ; Ray M
    Am J Med Genet; 1983 Mar; 14(3):479-85. PubMed ID: 6859101
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Familial lecithin:cholesterol acyltransferase deficiency - a new metabolic disease with renal involvement.
    Gjone E
    Adv Nephrol Necker Hosp; 1981; 10():167-85. PubMed ID: 6791468
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 6.