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46. Lipaemia retinalis in a 29-day-old infant with type 1 hyperlipoproteinaemia. Hayasaka S; Fukuyo T; Kitaoka M; Suzuki H; Omura K; Kondo Y; Nakagawa M Br J Ophthalmol; 1985 Apr; 69(4):280-2. PubMed ID: 3994945 [TBL] [Abstract][Full Text] [Related]
47. Hyperlipoproteinaemia and dietary fat modification in haemodialysis and renal transplant patients. Wahlqvist ML; Hurley BP Med J Aust; 1977 Aug; 2(7):207-8. PubMed ID: 333248 [TBL] [Abstract][Full Text] [Related]
48. Changes in endogenous plasma triglycerides during alimentary lipaemia in man studies with a density gradient. Fröberg S; Hallberg D J Atheroscler Res; 1968; 8(6):991-4. PubMed ID: 5707807 [No Abstract] [Full Text] [Related]
49. Classification of hyperlipoproteinaemias by computer interpretation. Loughlin JF; Leung FY; Henderson AR Ann Clin Biochem; 1984 Jul; 21 ( Pt 4)():326-31. PubMed ID: 6486708 [TBL] [Abstract][Full Text] [Related]
51. Letter: A plea for early diagnosis of hyperlipoproteinaemia. Watermeyer G S Afr Med J; 1976 May; 50(20):759. PubMed ID: 935946 [No Abstract] [Full Text] [Related]
52. Fundoscopic characteristics in three cases of familial hyperchylomicronaemia. López-Herrero F; Trujillo-Berraquero L; Franco-Ruedas C; Martínez-Borrego A; De Las Morenas-Iglesias J; Sánchez-Vicente JL Arch Soc Esp Oftalmol (Engl Ed); 2020 Dec; 95(12):611-614. PubMed ID: 32593602 [TBL] [Abstract][Full Text] [Related]
53. Phenotypic expression of heterozygous lipoprotein lipase deficiency in the extended pedigree of a proband homozygous for a missense mutation. Wilson DE; Emi M; Iverius PH; Hata A; Wu LL; Hillas E; Williams RR; Lalouel JM J Clin Invest; 1990 Sep; 86(3):735-50. PubMed ID: 2394828 [TBL] [Abstract][Full Text] [Related]
54. A missense mutation at codon 188 of the human lipoprotein lipase gene is a frequent cause of lipoprotein lipase deficiency in persons of different ancestries. Monsalve MV; Henderson H; Roederer G; Julien P; Deeb S; Kastelein JJ; Peritz L; Devlin R; Bruin T; Murthy MR J Clin Invest; 1990 Sep; 86(3):728-34. PubMed ID: 1975597 [TBL] [Abstract][Full Text] [Related]
55. The lipoprotein lipase Gly188----Glu mutation in South Africans of Indian descent: evidence suggesting common origins and an increased frequency. Henderson HE; Hassan F; Berger GM; Hayden MR J Med Genet; 1992 Feb; 29(2):119-22. PubMed ID: 1351946 [TBL] [Abstract][Full Text] [Related]
56. Familial hyperchylomicronaemia in four families. Problems in diagnosis, management, and aetiology reviewed. Berger GM; Bonnici F S Afr Med J; 1977 Apr; 51(18):623-8. PubMed ID: 867182 [TBL] [Abstract][Full Text] [Related]
57. Chylomicron and very-low-density lipoprotein levels in type I hyperlipoproteinaemia. The role of the liver in determining biochemical phenotype. Berger GM; Van der Westhuyzen JH; Huskisson J; Bonnici F; Henderson HE S Afr Med J; 1982 Feb; 61(8):266-72. PubMed ID: 7058458 [TBL] [Abstract][Full Text] [Related]
58. Evidence for a common, saturable, triglyceride removal mechanism for chylomicrons and very low density lipoproteins in man. Brunzell JD; Hazzard WR; Porte D; Bierman EL J Clin Invest; 1973 Jul; 52(7):1578-85. PubMed ID: 4352459 [TBL] [Abstract][Full Text] [Related]
59. Selective protamine sulphate inactivation of lipoprotein lipase and hepatic lipase in human post-heparin plasma: specific lipase levels in normals and in type I hyperlipoproteinaemia. Berger GM; Abraham PR Clin Chim Acta; 1977 Dec; 81(3):219-28. PubMed ID: 923094 [TBL] [Abstract][Full Text] [Related]