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.
123 related articles for article (PubMed ID: 10702948)
1. [Clinical manifestations of heterozygote familial hypercholesterolemia in Spain. Study of 301 cases from the central and northern areas]. Garcés C; Rodríguez Artalejo F; Serrano A; González Bonillo J; Almagro F; Garrido JA; Zúñiga M; de Oya M Med Clin (Barc); 2000 Jan; 114(2):50-1. PubMed ID: 10702948 [TBL] [Abstract][Full Text] [Related]
2. Moderate phenotypic expression of familial hypercholesterolemia in Tunisia. Jelassi A; Slimani A; Jguirim I; Najah M; Abid A; Boughamoura L; Mzid J; Fkih M; Maatouk F; Rouis M; Varret M; Slimane MN Clin Chim Acta; 2010 May; 411(9-10):735-8. PubMed ID: 20144596 [TBL] [Abstract][Full Text] [Related]
3. [Diagnostic and functional significance of arcus lipoides in hypercholesterolemia]. Schneider T; Ulbig M Fortschr Ophthalmol; 1991; 88(1):21-4. PubMed ID: 2045021 [TBL] [Abstract][Full Text] [Related]
4. Achilles tendon xanthomas are associated with the presence and burden of subclinical coronary atherosclerosis in heterozygous familial hypercholesterolemia: A pilot study. Mangili LC; Miname MH; Silva PRS; Bittencourt MS; Rocha VZ; Mangili OC; Salgado Filho W; Chacra AP; Jannes CE; Pereira AC; Santos RD Atherosclerosis; 2017 Aug; 263():393-397. PubMed ID: 28499609 [TBL] [Abstract][Full Text] [Related]
5. Familial hypercholesterolaemia: A guide for general practice. Brett T; Arnold-Reed D Aust J Gen Pract; 2019 Sep; 48(9):650-652. PubMed ID: 31476827 [No Abstract] [Full Text] [Related]
6. Polymorphism at the TRIB1 gene modulates plasma lipid levels: insight from the Spanish familial hypercholesterolemia cohort study. Garcia-Rios A; Perez-Martinez P; Mata P; Fuentes F; Lopez-Miranda J; Alonso R; Caballero J; Mata N; Perez-Jimenez F; Ordovas JM Nutr Metab Cardiovasc Dis; 2011 Dec; 21(12):957-63. PubMed ID: 20692138 [TBL] [Abstract][Full Text] [Related]
7. Evaluation of clinical and laboratory parameters used in the identification of index cases for genetic screening of familial hypercholesterolemia in Brazil. Silva PRS; Jannes CE; Oliveira TGM; Miname MH; Rocha VZ; Chacra AP; Gurgel MHC; Montenegro RM; Rodrigues Sobrinho CRM; Bello Moreira AS; Assad MHV; Pinto MRC; Tada MT; Santos RD; Pereira AC; Krieger JE Atherosclerosis; 2017 Aug; 263():257-262. PubMed ID: 28689098 [TBL] [Abstract][Full Text] [Related]
8. Association Between Cholesterol Efflux Capacity and Atherosclerotic Cardiovascular Disease in Patients With Familial Hypercholesterolemia. Ogura M; Hori M; Harada-Shiba M Arterioscler Thromb Vasc Biol; 2016 Jan; 36(1):181-8. PubMed ID: 26543100 [TBL] [Abstract][Full Text] [Related]
9. Corneal arcus and xanthomas in homozygous familial hypercholesterolemia: first report from China. Meng X; Lin J; Gao X; Guo J; Xin C; Wang J Indian J Ophthalmol; 2013 Dec; 61(12):770-1. PubMed ID: 24088637 [TBL] [Abstract][Full Text] [Related]
10. ["Gout tophi" and heart disease in the family]. Widmer Ch; Hättenschwiler A; Gross B; Schulthess G Praxis (Bern 1994); 2003 Nov; 92(45):1912-5. PubMed ID: 14639818 [TBL] [Abstract][Full Text] [Related]
11. Pediatric implications of heterozygous familial hypercholesterolemia. Screening and dietary treatment. Kwiterovich PO Arteriosclerosis; 1989; 9(1 Suppl):I111-20. PubMed ID: 2563219 [TBL] [Abstract][Full Text] [Related]
12. The molecular genetic basis and diagnosis of familial hypercholesterolemia in Denmark. Jensen HK Dan Med Bull; 2002 Nov; 49(4):318-45. PubMed ID: 12553167 [TBL] [Abstract][Full Text] [Related]
13. Differences in characteristics and risk of cardiovascular disease in familial hypercholesterolemia patients with and without tendon xanthomas: a systematic review and meta-analysis. Oosterveer DM; Versmissen J; Yazdanpanah M; Hamza TH; Sijbrands EJ Atherosclerosis; 2009 Dec; 207(2):311-7. PubMed ID: 19439299 [TBL] [Abstract][Full Text] [Related]
14. Selective screening for familial hypercholesterolemia in Austrian children - first year results. Kreissl A; Walleczek N; Espina PR; Hallwirth U; Greber-Platzer S BMC Pediatr; 2019 Jun; 19(1):208. PubMed ID: 31238984 [TBL] [Abstract][Full Text] [Related]
15. Treatment Gaps in Adults With Heterozygous Familial Hypercholesterolemia in the United States: Data From the CASCADE-FH Registry. deGoma EM; Ahmad ZS; O'Brien EC; Kindt I; Shrader P; Newman CB; Pokharel Y; Baum SJ; Hemphill LC; Hudgins LC; Ahmed CD; Gidding SS; Duffy D; Neal W; Wilemon K; Roe MT; Rader DJ; Ballantyne CM; Linton MF; Duell PB; Shapiro MD; Moriarty PM; Knowles JW Circ Cardiovasc Genet; 2016 Jun; 9(3):240-9. PubMed ID: 27013694 [TBL] [Abstract][Full Text] [Related]
16. Long-term probucol treatment results in regression of xanthomas, but in progression of coronary atherosclerosis in a heterozygous patient with familial hypercholesterolemia. Kajinami K; Nishitsuji M; Takeda Y; Shimizu M; Koizumi J; Mabuchi H Atherosclerosis; 1996 Feb; 120(1-2):181-7. PubMed ID: 8645359 [TBL] [Abstract][Full Text] [Related]
17. A keen eye for risk. Ford TJ; Rocchiccioli P BMJ; 2018 Feb; 360():j5884. PubMed ID: 29419393 [No Abstract] [Full Text] [Related]
18. [Homozygous familial hypercholesterolemia: development and a case illustration]. Choukri M; Laaroussi N; Taheri H; Chabraoui L Ann Biol Clin (Paris); 2013; 71(1):99-103. PubMed ID: 23396432 [TBL] [Abstract][Full Text] [Related]
19. Plasma triglycerides related decrease in high-density lipoprotein cholesterol and its association with myocardial infarction in heterozygous familial hypercholesterolemia. Moorjani S; Gagné C; Lupien PJ; Brun D Metabolism; 1986 Apr; 35(4):311-6. PubMed ID: 3959903 [TBL] [Abstract][Full Text] [Related]
20. Homozygous familial hypercholesterolaemia presenting with cutaneous xanthomas: response to liver transplantation. Moyle M; Tate B Australas J Dermatol; 2004 Nov; 45(4):226-8. PubMed ID: 15527434 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]