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22. Unusual xanthomas in a young patient with heterozygous familial hypercholesterolemia and type III hyperlipoproteinemia. Feussner G; Dobmeyer J; Nissen H; Hansen TS Am J Med Genet; 1996 Oct; 65(2):149-54. PubMed ID: 8911609 [TBL] [Abstract][Full Text] [Related]
23. Severe familial hypercholesterolaemia: current and future management. Farnier M; Bruckert E Arch Cardiovasc Dis; 2012 Dec; 105(12):656-65. PubMed ID: 23199621 [TBL] [Abstract][Full Text] [Related]
24. [Familial hypercholesterolemia: A largely underestimated cardiovascular risk]. Ferrières J; Bruckert É; Béliard S; Rabès JP; Farnier M; Krempf M; Cariou B; Danchin N Ann Cardiol Angeiol (Paris); 2018 Feb; 67(1):1-8. PubMed ID: 28576280 [TBL] [Abstract][Full Text] [Related]
26. Sonographic detection of xanthomas in normal-sized Achilles' tendons of individuals with heterozygous familial hypercholesterolemia. Bude RO; Nesbitt SD; Adler RS; Rubenfire M AJR Am J Roentgenol; 1998 Mar; 170(3):621-5. PubMed ID: 9490941 [TBL] [Abstract][Full Text] [Related]
27. Multiple Ligation-dependent Probe Amplification Along with Whole Exome Sequencing Should be Required for the Diagnosis of Structural Heterozygous Familial Hypercholesteremia. Saotome M; Maekawa Y Intern Med; 2022; 61(19):2829-2830. PubMed ID: 36184533 [No Abstract] [Full Text] [Related]
29. Guidelines for the diagnosis and management of heterozygous familial hypercholesterolemia. Civeira F; Atherosclerosis; 2004 Mar; 173(1):55-68. PubMed ID: 15177124 [TBL] [Abstract][Full Text] [Related]
30. Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study. Pirillo A; Garlaschelli K; Arca M; Averna M; Bertolini S; Calandra S; Tarugi P; Catapano AL; Atheroscler Suppl; 2017 Oct; 29():17-24. PubMed ID: 28965616 [TBL] [Abstract][Full Text] [Related]
34. Seven-year clinical follow-up of a Chinese homozygous familial hypercholesterolemia child with premature xanthomas and coronary artery disease--a need for early diagnosis and aggressive treatment. Jiang L; Gao F; Hu LB; Sun LY; Pan XD; Lin J; Zhang HB; Yong Q; Wang Q; Yang Y; Wang CM; Yang SW; Zhang F; Wang LY Int J Cardiol; 2014 Nov; 177(1):188-91. PubMed ID: 25499375 [No Abstract] [Full Text] [Related]
35. Hypolipidemic treatment of heterozygous familial hypercholesterolemia: a lifelong challenge. Vuorio AF; Kovanen PT; Gylling H Expert Rev Cardiovasc Ther; 2004 May; 2(3):405-15. PubMed ID: 15151486 [TBL] [Abstract][Full Text] [Related]
36. Double-filtration plasmapheresis in heterozygous familial hypercholesterolemia: our experience over 25 treatments. Candrina R; Spandrio S; Di Stefano O; Scalvini T; Cotelli M; Tosoni M; Giustina G Beitr Infusionsther; 1988; 23():189-90. PubMed ID: 2484776 [No Abstract] [Full Text] [Related]
37. Genetic risk factors in the development of heart disease: familial hypercholesterolemia and hyperhomocysteinemia. LaCharity LA AACN Clin Issues; 1998 Nov; 9(4):531-8. PubMed ID: 9855863 [TBL] [Abstract][Full Text] [Related]
38. Familial hypercholesterolemia: current treatment and advances in management. Huijgen R; Vissers MN; Defesche JC; Lansberg PJ; Kastelein JJ; Hutten BA Expert Rev Cardiovasc Ther; 2008 Apr; 6(4):567-81. PubMed ID: 18402545 [TBL] [Abstract][Full Text] [Related]