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.
472 related articles for article (PubMed ID: 30876530)
1. Variable expression and penetrance in Portuguese families with Familial Hypercholesterolemia with mild phenotype. Gaspar IM; Gaspar A Atheroscler Suppl; 2019 Mar; 36():28-30. PubMed ID: 30876530 [TBL] [Abstract][Full Text] [Related]
2. 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]
3. DIAgnosis and Management Of familial hypercholesterolemia in a Nationwide Design (DIAMOND-FH): Prevalence in Switzerland, clinical characteristics and the diagnostic value of clinical scores. Miserez AR; Martin FJ; Spirk D Atherosclerosis; 2018 Oct; 277():282-288. PubMed ID: 30270060 [TBL] [Abstract][Full Text] [Related]
5. Lipid phenotype and heritage pattern in families with genetic hypercholesterolemia not related to LDLR, APOB, PCSK9, or APOE. Jarauta E; Pérez-Ruiz MR; Pérez-Calahorra S; Mateo-Gallego R; Cenarro A; Cofán M; Ros E; Civeira F; Tejedor MT J Clin Lipidol; 2016; 10(6):1397-1405.e2. PubMed ID: 27919357 [TBL] [Abstract][Full Text] [Related]
6. Mutational analysis of the LDLR gene in a cohort of Colombian families with familial hypercholesterolemia. López G; Bernal LM; Gelvez N; Gómez LF; Nova A; Sánchez AI; Tamayo ML Atherosclerosis; 2018 Oct; 277():434-439. PubMed ID: 30270082 [TBL] [Abstract][Full Text] [Related]
7. Causative mutations and premature cardiovascular disease in patients with heterozygous familial hypercholesterolaemia. Rubba P; Gentile M; Marotta G; Iannuzzi A; Sodano M; De Simone B; Jossa F; Iannuzzo G; Giacobbe C; Di Taranto MD; Fortunato G Eur J Prev Cardiol; 2017 Jul; 24(10):1051-1059. PubMed ID: 28353356 [TBL] [Abstract][Full Text] [Related]
8. The type of mutation in the low density lipoprotein receptor gene influences the cholesterol-lowering response of the HMG-CoA reductase inhibitor simvastatin in patients with heterozygous familial hypercholesterolaemia. Heath KE; Gudnason V; Humphries SE; Seed M Atherosclerosis; 1999 Mar; 143(1):41-54. PubMed ID: 10208479 [TBL] [Abstract][Full Text] [Related]
9. A Chinese homozygote of familial hypercholesterolemia: identification of a novel C263R mutation in the LDL receptor gene. Wang D; Wu B; Li Y; Heng W; Zhong H; Mu Y; Wang J J Hum Genet; 2001; 46(3):152-4. PubMed ID: 11310584 [TBL] [Abstract][Full Text] [Related]
10. Genetics and kinetics of familial hypercholesterolemia, with the special focus on FH-(Marburg) p.W556R. Soufi M; Kurt B; Schweer H; Sattler AM; Klaus G; Zschocke J; Schaefer JR Atheroscler Suppl; 2009 Dec; 10(5):5-11. PubMed ID: 20129366 [TBL] [Abstract][Full Text] [Related]
11. Spectrum of mutations in index patients with familial hypercholesterolemia in Singapore: Single center study. Pek SLT; Dissanayake S; Fong JCW; Lin MX; Chan EZL; Tang JI; Lee CW; Ong HY; Sum CF; Lim SC; Tavintharan S Atherosclerosis; 2018 Feb; 269():106-116. PubMed ID: 29353225 [TBL] [Abstract][Full Text] [Related]
12. First case report of familial hypercholesterolemia in an Omani family due to novel mutation in the low-density lipoprotein receptor gene. Al-Hinai AT; Al-Abri A; Al-Dhuhli H; Al-Waili K; Al-Sabti H; Al-Yaarubi S; Al-Hashmi K; Banerjee Y; Al-Zakwani I; Al-Rasadi K Angiology; 2013 May; 64(4):287-92. PubMed ID: 23162007 [TBL] [Abstract][Full Text] [Related]
14. Cascade screening and genetic diagnosis of familial hypercholesterolemia in clusters of the Southeastern region from Brazil. de Paiva Silvino JP; Jannes CE; Tada MT; Lima IR; Silva IFO; Pereira AC; Gomes KB Mol Biol Rep; 2020 Dec; 47(12):9279-9288. PubMed ID: 33231818 [TBL] [Abstract][Full Text] [Related]
15. Homozygous familial hypercholesterolaemia in Vietnam: Case series, genetics and cascade testing of families. Truong TH; Kim NT; Nguyen MNT; Pang J; Hooper AJ; Watts GF; Do DL Atherosclerosis; 2018 Oct; 277():392-398. PubMed ID: 30270076 [TBL] [Abstract][Full Text] [Related]
16. Novel combined variants of LDLR and LDLRAP1 genes causing severe familial hypercholesterolemia. Alnouri F; Athar M; Al-Allaf FA; Abduljaleel Z; Taher MM; Bouazzaoui A; Al Ammari D; Karrar H; Albabtain M Atherosclerosis; 2018 Oct; 277():425-433. PubMed ID: 30270081 [TBL] [Abstract][Full Text] [Related]
18. Relationship of Familial Hypercholesterolemia and High Low-Density Lipoprotein Cholesterol to Ischemic Stroke: Copenhagen General Population Study. Beheshti S; Madsen CM; Varbo A; Benn M; Nordestgaard BG Circulation; 2018 Aug; 138(6):578-589. PubMed ID: 29593013 [TBL] [Abstract][Full Text] [Related]
19. Low density lipoprotein--receptor (LDL-R) gene mutations among Filipinos with familial hypercholesterolemia. Punzalan FE; Sy RG; Santos RS; Cutiongco EM; Gosiengfiao S; Fadriguilan E; George P; Laurie A J Atheroscler Thromb; 2005; 12(5):276-83. PubMed ID: 16205024 [TBL] [Abstract][Full Text] [Related]
20. [Genotype-phenotype analysis of a homozygous familial hypercholesterolemia pedigree]. Wang DY; Zhang YM; Che FY; Chu JP; Zhang LY; Li H; Liu BL; Yao ZY; Zhao YW Zhonghua Er Ke Za Zhi; 2020 Feb; 58(2):101-106. PubMed ID: 32102145 [No Abstract] [Full Text] [Related] [Next] [New Search]