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1
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84900562085
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What is new with familial hypercholesterolemia?
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COI: 1:CAS:528:DC%2BC2cXnsFeks7o%3D, PID: 24699416, This article comprehensively reviews the underdiagnosed and high-risk nature of familial hypercholesterolemia. It also highlights the FH-associated subclinical disease and novel treatments that will take aim at reducing the burden of severely increased levels of cholesterol
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Santos RD, Maranhao RC. What is new with familial hypercholesterolemia? Curr Opin Lipidol. 2014;25:183–8. This article comprehensively reviews the underdiagnosed and high-risk nature of familial hypercholesterolemia. It also highlights the FH-associated subclinical disease and novel treatments that will take aim at reducing the burden of severely increased levels of cholesterol.
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(2014)
Curr Opin Lipidol
, vol.25
, pp. 183-188
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Santos, R.D.1
Maranhao, R.C.2
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2
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84868628467
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Familial hypercholesterolemia in the Danish population: Prevalence, coronary artery disease, and cholesterol-lowering medication
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COI: 1:CAS:528:DC%2BC38Xhs12kurfL, PID: 22893714
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Benn W, Watts GF, Tybjaerg-Hansen A, Nordestgaard BG. Familial hypercholesterolemia in the Danish population: prevalence, coronary artery disease, and cholesterol-lowering medication. J Clin Endocrinol Metab. 2012;97:3956–64.
-
(2012)
J Clin Endocrinol Metab
, vol.97
, pp. 3956-3964
-
-
Benn, W.1
Watts, G.F.2
Tybjaerg-Hansen, A.3
Nordestgaard, B.G.4
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3
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84900832381
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The severe hypercholesterolemia phenotype: Clinical diagnosis, management, and emerging therapies
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COI: 1:CAS:528:DC%2BC2cXmtFWjtLg%3D, PID: 24632267, In this state of the art paper, experts cover the clinical diagnosis, management, and emerging therapies that are associated with FH. They also recommend ways to efficiently utilize cascade screening and genetic testing to increase the detection of unknown cases of familial hypercholesterolemia
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Sniderman AD, Tsimikas S, Fazio S. The severe hypercholesterolemia phenotype: clinical diagnosis, management, and emerging therapies. J Am Coll Cardiol. 2014;63:1935–47. In this state of the art paper, experts cover the clinical diagnosis, management, and emerging therapies that are associated with FH. They also recommend ways to efficiently utilize cascade screening and genetic testing to increase the detection of unknown cases of familial hypercholesterolemia.
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(2014)
J Am Coll Cardiol
, vol.63
, pp. 1935-1947
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Sniderman, A.D.1
Tsimikas, S.2
Fazio, S.3
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4
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84876167878
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Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolemia: A case-control study
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COI: 1:CAS:528:DC%2BC3sXivFOqs7Y%3D, PID: 23433573, In this study, which genotyped for 12 common LDL-C-raising alleles in order to compare gene score distribution among different participants and controls, mutation negative patients were recognized to have significantly higher LDL-C scores. Also, in patients with FH, but no known mutation, a polygenic cause is considered, and cascade screening procedures should adjust accordingly
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Talmud PJ, Shah S, Whittall R, et al. Use of low-density lipoprotein cholesterol gene score to distinguish patients with polygenic and monogenic familial hypercholesterolemia: a case-control study. Lancet. 2013;381:1293–301. In this study, which genotyped for 12 common LDL-C-raising alleles in order to compare gene score distribution among different participants and controls, mutation negative patients were recognized to have significantly higher LDL-C scores. Also, in patients with FH, but no known mutation, a polygenic cause is considered, and cascade screening procedures should adjust accordingly.
-
(2013)
Lancet
, vol.381
, pp. 1293-1301
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Talmud, P.J.1
Shah, S.2
Whittall, R.3
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5
-
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33748787440
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Diagnosing familial hypercholesterolaemia: The relevance of genetic testing
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PID: 16825289
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Van Aalst-Cohen ES, Jansen AC, Tanck MW. Diagnosing familial hypercholesterolaemia: the relevance of genetic testing. Eur Heart J. 2006;27:2240–6.
-
(2006)
Eur Heart J
, vol.27
, pp. 2240-2246
-
-
Van Aalst-Cohen, E.S.1
Jansen, A.C.2
Tanck, M.W.3
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6
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79956278397
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Familial hypercholesterolemias: Prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia
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PID: 21600530
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Hopkins PN, Toth PP, Ballantyne CM, Rader DJ. Familial hypercholesterolemias: prevalence, genetics, diagnosis and screening recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. J Clin Lipidol. 2011;5:S9–17.
-
(2011)
J Clin Lipidol
, vol.5
, pp. S9-S17
-
-
Hopkins, P.N.1
Toth, P.P.2
Ballantyne, C.M.3
Rader, D.J.4
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7
-
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77955053533
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Cholesterol, the central lipid of mammalian cells
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COI: 1:CAS:528:DC%2BC3cXpt12ltL8%3D, PID: 20627678
-
Maxfield FR, van Meer G. Cholesterol, the central lipid of mammalian cells. Curr Opin Cell Biol. 2010;22:422–9.
-
(2010)
Curr Opin Cell Biol
, vol.22
, pp. 422-429
-
-
Maxfield, F.R.1
van Meer, G.2
-
8
-
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84906716305
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A position paper from the Consensus Panel on Familial Hypercholesterolemia of the European Atherosclerosis Society, Eur Heart J:
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Cuchel M, Bruckert E, Ginsberg HN, Raal FJ, Santos RD, Hegele RA, et al. Homozygous familial hypercholesterolemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolemia of the European Atherosclerosis Society. Eur Heart J. 2014.
-
(2014)
Homozygous familial hypercholesterolemia: New insights and guidance for clinicians to improve detection and clinical management
-
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Cuchel, M.1
Bruckert, E.2
Ginsberg, H.N.3
Raal, F.J.4
Santos, R.D.5
Hegele, R.A.6
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9
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84864772507
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Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment
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COI: 1:CAS:528:DC%2BC38XjtlSlsbk%3D, PID: 22398274, This important review discussed the diagnostic criteria for HoFH, as defined in multiple studies. With an emphasis on the history of HoFH, this review covered the effectiveness of current therapy and the excitement surrounding future novel therapies
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Raal FJ, Santos RD. Homozygous familial hypercholesterolemia: current perspectives on diagnosis and treatment. Atherosclerosis. 2012;223:262–8. This important review discussed the diagnostic criteria for HoFH, as defined in multiple studies. With an emphasis on the history of HoFH, this review covered the effectiveness of current therapy and the excitement surrounding future novel therapies.
-
(2012)
Atherosclerosis
, vol.223
, pp. 262-268
-
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Raal, F.J.1
Santos, R.D.2
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10
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84871869008
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Guidelines for the management of familial hypercholesterolemia
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COI: 1:CAS:528:DC%2BC3sXjsFGntL8%3D, PID: 23095242
-
Harada-Shiba M, Arai H, Oikawa S, Ohta T, Okada T, Okamura T, et al. Guidelines for the management of familial hypercholesterolemia. J Atheroscler Thromb. 2012;19(12):1043–60.
-
(2012)
J Atheroscler Thromb
, vol.19
, Issue.12
, pp. 1043-1060
-
-
Harada-Shiba, M.1
Arai, H.2
Oikawa, S.3
Ohta, T.4
Okada, T.5
Okamura, T.6
-
11
-
-
84875919777
-
Imaging biomarkers to track subclinical atherosclerosis in heterozygous familial hypercholesterolemia
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Miname MH, Santos RD. Imaging biomarkers to track subclinical atherosclerosis in heterozygous familial hypercholesterolemia. Clin Lipidol. 2013;8:1–12.
-
(2013)
Clin Lipidol
, vol.8
, pp. 1-12
-
-
Miname, M.H.1
Santos, R.D.2
-
12
-
-
0016373413
-
Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia
-
COI: 1:STN:280:DyaE2c7gtVegsw%3D%3D, PID: 4813182
-
Stone NJ, Levy RI, Fredrickson DS. Coronary artery disease in 116 kindred with familial type II hyperlipoproteinemia. Circulation. 1974;49:476–88.
-
(1974)
Circulation
, vol.49
, pp. 476-488
-
-
Stone, N.J.1
Levy, R.I.2
Fredrickson, D.S.3
-
13
-
-
0014693152
-
Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states
-
COI: 1:STN:280:DyaE3c%2Fms1ajsw%3D%3D, PID: 4188273
-
Slack J. Risks of ischaemic heart-disease in familial hyperlipoproteinaemic states. Lancet. 1969;2:1380–2.
-
(1969)
Lancet
, vol.2
, pp. 1380-1382
-
-
Slack, J.1
-
14
-
-
0021236065
-
Cardiovascular features of homozygous familial hypercholesterolemia: Analysis of 16 patients
-
COI: 1:STN:280:DyaL2c3ltlGhtg%3D%3D, PID: 6331147
-
Sprecher DL, Schaefer EJ, Kent KM, et al. Cardiovascular features of homozygous familial hypercholesterolemia: analysis of 16 patients. Am J Cardiol. 1984;54:20–30.
-
(1984)
Am J Cardiol
, vol.54
, pp. 20-30
-
-
Sprecher, D.L.1
Schaefer, E.J.2
Kent, K.M.3
-
15
-
-
84890461947
-
Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: Guidance for clinicians to prevent coronary heart disease: Consensus statement of the European Atherosclerosis Society
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COI: 1:CAS:528:DC%2BC3sXhvVOqu7vI, PID: 23956253
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Nordestgaard BG, Chapman M, Humphries SE. Familial hypercholesterolaemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: consensus statement of the European Atherosclerosis Society. Eur Heart J. 2013;34:3478–90.
-
(2013)
Eur Heart J
, vol.34
, pp. 3478-3490
-
-
Nordestgaard, B.G.1
Chapman, M.2
Humphries, S.E.3
-
16
-
-
84890403508
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Enhancing physicians use of clinical guidelines
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COI: 1:CAS:528:DC%2BC2cXpvFCnsg%3D%3D, PID: 24310916, This commentary on the importance of checklists convinced us to consolidate the current guidelines into a checklist that highlights FH recommendations
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Pronovost PJ. Enhancing physicians use of clinical guidelines. JAMA. 2013;310:2501–2. This commentary on the importance of checklists convinced us to consolidate the current guidelines into a checklist that highlights FH recommendations.
-
(2013)
JAMA
, vol.310
, pp. 2501-2502
-
-
Pronovost, P.J.1
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17
-
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84893647246
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Integrated guidance on the care of familial hypercholesterolemia from the International FH Foundation
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PID: 24418289, This paper, led by an esteemed group of FH experts, covered the guidelines for detecting, screening, testing, and managing adults and children with familial hypercholesterolemia. Each guideline recommendation also covered the level of evidence and grades of recommendation
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Watts GF, Gidding S, Wierzbicki AS, et al. Integrated guidance on the care of familial hypercholesterolemia from the International FH Foundation. Int J Cardiol. 2014;171:309–25. This paper, led by an esteemed group of FH experts, covered the guidelines for detecting, screening, testing, and managing adults and children with familial hypercholesterolemia. Each guideline recommendation also covered the level of evidence and grades of recommendation.
-
(2014)
Int J Cardiol
, vol.171
, pp. 309-325
-
-
Watts, G.F.1
Gidding, S.2
Wierzbicki, A.S.3
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18
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79956267846
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Familial hypercholesterolemia: Screening, diagnosis and management of pediatric and adult patients: Clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia
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PID: 21600525, This article provided expert US guidance on the expert recommendations for improving screening, detection, and treatment of both adults and children with familial hypercholesterolemia
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Goldberg AC, Hopkins PN, Toth PP. Familial hypercholesterolemia: screening, diagnosis and management of pediatric and adult patients: clinical guidance from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. J Clin Lipidol. 2011;5:S1–8. This article provided expert US guidance on the expert recommendations for improving screening, detection, and treatment of both adults and children with familial hypercholesterolemia.
-
(2011)
J Clin Lipidol
, vol.5
, pp. S1-S8
-
-
Goldberg, A.C.1
Hopkins, P.N.2
Toth, P.P.3
-
19
-
-
84055213533
-
-
Expert Panel on Integrated Guidelines for Cardiovascular Health and Risk Reduction in Children and Adolescents: summary report
-
Expert Panel on Integrated Guidelines for Cardiovascular Health and Risk Reduction in Children and Adolescents: summary report. Pediatrics. 2011;128:S213.
-
(2011)
Pediatrics
, vol.128
, pp. S213
-
-
-
20
-
-
79956263939
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Pediatric aspects of familial hypercholesterolemias: Recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia
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PID: 21600527, With increased opportunity for improvement, children with FH require dedicated attention and evidence-guided recommendations. In this paper, FH experts consolidated a set of specific recommendations to help improve the prognoses and progression of children with familial hypercholesterolemia
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Daniels SR, Gidding SS, de Ferranti SD. Pediatric aspects of familial hypercholesterolemias: recommendations from the National Lipid Association Expert Panel on Familial Hypercholesterolemia. J Clin Lipidol. 2011;5:S30–7. With increased opportunity for improvement, children with FH require dedicated attention and evidence-guided recommendations. In this paper, FH experts consolidated a set of specific recommendations to help improve the prognoses and progression of children with familial hypercholesterolemia.
-
(2011)
J Clin Lipidol
, vol.5
, pp. S30-S37
-
-
Daniels, S.R.1
Gidding, S.S.2
de Ferranti, S.D.3
-
22
-
-
4444376916
-
Genetic causes of monogenic heterozygous familial hypercholesterolemia: A huge prevalence review
-
PID: 15321837
-
Austin MA, Hutter CM, Zimmern RL, Humprhies SE. Genetic causes of monogenic heterozygous familial hypercholesterolemia: a huge prevalence review. Am J Epidemiol. 2004;160(5):407–20.
-
(2004)
Am J Epidemiol
, vol.160
, Issue.5
, pp. 407-420
-
-
Austin, M.A.1
Hutter, C.M.2
Zimmern, R.L.3
Humprhies, S.E.4
-
23
-
-
0027301629
-
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics
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COI: 1:STN:280:DyaK3szhvVOnuw%3D%3D, PID: 8328379
-
Williams RR, Hunt SC, Schumacher MC, Hegele RA, Leppert MF, Ludwig EH, et al. Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am J Cardiol. 1993;72(2):171–6.
-
(1993)
Am J Cardiol
, vol.72
, Issue.2
, pp. 171-176
-
-
Williams, R.R.1
Hunt, S.C.2
Schumacher, M.C.3
Hegele, R.A.4
Leppert, M.F.5
Ludwig, E.H.6
-
24
-
-
84876161625
-
Polygenic familial hypercholesterolemia: Does it matter?
-
PID: 23433574
-
Stein EA, Raal FJ. Polygenic familial hypercholesterolemia: does it matter? Lancet. 2013;381:1255–7.
-
(2013)
Lancet
, vol.381
, pp. 1255-1257
-
-
Stein, E.A.1
Raal, F.J.2
-
25
-
-
79959332777
-
Efficacy of statins in familial hypercholesterolaemia: A long term cohort study
-
PID: 19001495
-
Versmissen J, Oosterveer DM, Yazdanpanah M. Efficacy of statins in familial hypercholesterolaemia: a long term cohort study. BMJ. 2008;337:a2423.
-
(2008)
BMJ
, vol.337
, pp. a2423
-
-
Versmissen, J.1
Oosterveer, D.M.2
Yazdanpanah, M.3
-
26
-
-
79959747118
-
Atheroprotective reverse cholesterol transport pathway is defective in familial hypercholesterolemia
-
COI: 1:CAS:528:DC%2BC3MXnslSgurY%3D, PID: 21527752
-
Bellanger N, Orsoni A, Julia Z, et al. Atheroprotective reverse cholesterol transport pathway is defective in familial hypercholesterolemia. Arterioscler Thromb Vasc Biol. 2011;31:1675–81.
-
(2011)
Arterioscler Thromb Vasc Biol
, vol.31
, pp. 1675-1681
-
-
Bellanger, N.1
Orsoni, A.2
Julia, Z.3
-
27
-
-
84902576469
-
2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: A report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines
-
Stone NJ, Robinson J, Lichtenstein AH, Bairey Merz CN, Blum CB, Eckel RH, et al. 2013 ACC/AHA Guideline on the Treatment of Blood Cholesterol to Reduce Atherosclerotic Cardiovascular Risk in Adults: a report of the American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Circulation. 2013;63(25 Pt B):2889–934.
-
(2013)
Circulation
, vol.63
, pp. 2889-2934
-
-
Stone, N.J.1
Robinson, J.2
Lichtenstein, A.H.3
Bairey Merz, C.N.4
Blum, C.B.5
Eckel, R.H.6
-
28
-
-
79956277910
-
Management of familial hypercholesterolemia’s in adult patients: Recommendations from the National Lipid Association Expert Panel on Familial Hyperchoelsterolemia
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PID: 21600528
-
Ito MK, McGowan MP, Moriarty PM. Management of familial hypercholesterolemia’s in adult patients: recommendations from the National Lipid Association Expert Panel on Familial Hyperchoelsterolemia. J Clin Lipidol. 2011;5:S38–45.
-
(2011)
J Clin Lipidol
, vol.5
, pp. S38-S45
-
-
Ito, M.K.1
McGowan, M.P.2
Moriarty, P.M.3
-
29
-
-
84890461947
-
Familial hypercholesterolemia is underdiagnosed and undertreated in the general population: Guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society
-
COI: 1:CAS:528:DC%2BC3sXhvVOqu7vI, PID: 23956253
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Nordestgaard BG, Chapman MJ, Humphries SE, et al. Familial hypercholesterolemia is underdiagnosed and undertreated in the general population: guidance for clinicians to prevent coronary heart disease: Consensus Statement of the European Atherosclerosis Society. Eur Heart J. 2013;34:3478–90.
-
(2013)
Eur Heart J
, vol.34
, pp. 3478-3490
-
-
Nordestgaard, B.G.1
Chapman, M.J.2
Humphries, S.E.3
-
30
-
-
0242544064
-
Comparison of rosuvastatin versus atorvastatin in patients with heterozygous familial hypercholesterolemia
-
COI: 1:CAS:528:DC%2BD3sXptVWnsbc%3D, PID: 14636905
-
Stein EA, Strutt K, Southworth H, Diggle PJ, Miller E. Comparison of rosuvastatin versus atorvastatin in patients with heterozygous familial hypercholesterolemia. Am J Cardiol. 2003;92:1287–93.
-
(2003)
Am J Cardiol
, vol.92
, pp. 1287-1293
-
-
Stein, E.A.1
Strutt, K.2
Southworth, H.3
Diggle, P.J.4
Miller, E.5
-
31
-
-
0025685469
-
Regression of coronary atherosclerosis during treatment of familial hypercholesterolemia with combined drug regimens
-
COI: 1:STN:280:DyaK3M%2Fls1Knuw%3D%3D, PID: 2243428
-
Kane JP, Malloy MJ, Ports TA, Phillips NR, Diehl JC, Havel RJ. Regression of coronary atherosclerosis during treatment of familial hypercholesterolemia with combined drug regimens. JAMA. 1990;264:3007–12.
-
(1990)
JAMA
, vol.264
, pp. 3007-3012
-
-
Kane, J.P.1
Malloy, M.J.2
Ports, T.A.3
Phillips, N.R.4
Diehl, J.C.5
Havel, R.J.6
-
32
-
-
53449088738
-
Efficacy and safety of coadministration of ezetimibe and simvastatin in adolescents with heterozygous familial hypercholesterolemia
-
PID: 18940534
-
Van der Graaf A, Cuffie-Jackson C, Vissers MN, et al. Efficacy and safety of coadministration of ezetimibe and simvastatin in adolescents with heterozygous familial hypercholesterolemia. J Am Coll Cardiol. 2008;52:1421–9.
-
(2008)
J Am Coll Cardiol
, vol.52
, pp. 1421-1429
-
-
Van der Graaf, A.1
Cuffie-Jackson, C.2
Vissers, M.N.3
-
33
-
-
84887164358
-
Effect of proprotein convertase subtillisin/kexin 9 monoclonal antibody, AMG 145, in homozygous familial hypercholesterolemia
-
COI: 1:CAS:528:DC%2BC3sXhslaqu7fI, PID: 24014831
-
Stein EA, Honarpour N, Wasserman SM, Xu F, Scott R, Raal RJ. Effect of proprotein convertase subtillisin/kexin 9 monoclonal antibody, AMG 145, in homozygous familial hypercholesterolemia. Circulation. 2013;128:2113–20.
-
(2013)
Circulation
, vol.128
, pp. 2113-2120
-
-
Stein, E.A.1
Honarpour, N.2
Wasserman, S.M.3
Xu, F.4
Scott, R.5
Raal, R.J.6
-
34
-
-
84863494422
-
Effect of a monoclonal antibody to PCSK9, REGN727/SAR236553, to reduce low-density lipoprotein cholesterol in patients with heterozygous familial hypercholesterolaemia on stable statin dose with or without ezetimibe therapy: A phase 2 randomised controlled trial
-
COI: 1:CAS:528:DC%2BC38XnslShu7s%3D, PID: 22633824
-
Stein EA, Gipe D, Bergeron J, et al. Effect of a monoclonal antibody to PCSK9, REGN727/SAR236553, to reduce low-density lipoprotein cholesterol in patients with heterozygous familial hypercholesterolaemia on stable statin dose with or without ezetimibe therapy: a phase 2 randomised controlled trial. Lancet. 2012;380:29–36.
-
(2012)
Lancet
, vol.380
, pp. 29-36
-
-
Stein, E.A.1
Gipe, D.2
Bergeron, J.3
-
35
-
-
84869220345
-
Low-density lipoprotein cholesterol-lowering effects of AMG 145, a monoclonal antibody to proprotein convertase subtilisin/kexin type 9 serine protease in patients with heterozygous familial hypercholesterolemia: The Reduction of LDL-C with PCSK9 Inhibition in Heterozygous Familial Hypercholesterolemia Disorder (RUTHERFORD) randomized trial
-
COI: 1:CAS:528:DC%2BC38Xhs1Oltb7P, PID: 23129602
-
Raal F, Scott R, Somaratne R, et al. Low-density lipoprotein cholesterol-lowering effects of AMG 145, a monoclonal antibody to proprotein convertase subtilisin/kexin type 9 serine protease in patients with heterozygous familial hypercholesterolemia: the Reduction of LDL-C with PCSK9 Inhibition in Heterozygous Familial Hypercholesterolemia Disorder (RUTHERFORD) randomized trial. Circulation. 2012;126:2408–17.
-
(2012)
Circulation
, vol.126
, pp. 2408-2417
-
-
Raal, F.1
Scott, R.2
Somaratne, R.3
-
36
-
-
84890904215
-
Lipoprotein apheresis in patients with maximally tolerated lipid-lowering therapy, lipoprotein(a)-hyperlipoproteinemia and progressive cardiovascular disease: Prospective observational multicenter study
-
COI: 1:CAS:528:DC%2BC3sXhvF2ktLzF, PID: 24056686
-
Leebmann J, Roeseler E, Julius U, for the Pro(a)LiFe Study Group. Lipoprotein apheresis in patients with maximally tolerated lipid-lowering therapy, lipoprotein(a)-hyperlipoproteinemia and progressive cardiovascular disease: prospective observational multicenter study. Circulation. 2013;128:2567–76.
-
(2013)
Circulation
, vol.128
, pp. 2567-2576
-
-
Leebmann, J.1
Roeseler, E.2
-
38
-
-
0032535310
-
Long term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia. Hokuriku-FH-LDL-Apheresis Study Group
-
COI: 1:STN:280:DyaK1M%2FovFCnuw%3D%3D, PID: 9874053
-
Mabuchi H, Koizumi J, Chimizu M, et al. Long term efficacy of low-density lipoprotein apheresis on coronary heart disease in familial hypercholesterolemia. Hokuriku-FH-LDL-Apheresis Study Group. Am J Cardiol. 1998;82:1489–95.
-
(1998)
Am J Cardiol
, vol.82
, pp. 1489-1495
-
-
Mabuchi, H.1
Koizumi, J.2
Chimizu, M.3
-
41
-
-
84924366648
-
Homozygous autosomal dominant hypercholesterolemia in the Netherlands: Prevalence, genotype-phenotype relationship, and clinical outcome
-
PID: 24585268
-
Sjouke B, Kusters DM, Kindt I, et al. Homozygous autosomal dominant hypercholesterolemia in the Netherlands: prevalence, genotype-phenotype relationship, and clinical outcome. Eur Heart J. 2014. doi:10.1093/eurheartj/ehu058.
-
(2014)
Eur Heart J
-
-
Sjouke, B.1
Kusters, D.M.2
Kindt, I.3
-
42
-
-
84911433299
-
-
Statistics Netherlands (in Dutch: Centraal Bureau voor de Statistiek). (31 October 2012)
-
Statistics Netherlands (in Dutch: Centraal Bureau voor de Statistiek). https://www.cbs.nl (31 October 2012).
-
-
-
-
43
-
-
0015796295
-
Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia
-
COI: 1:STN:280:DyaE3s3itVGnsQ%3D%3D, PID: 4718953
-
Goldstein JL, Schrott HG, Hazzard WR, Bierman EL, Motulsky AG. Hyperlipidemia in coronary heart disease. II. Genetic analysis of lipid levels in 176 families and delineation of a new inherited disorder, combined hyperlipidemia. J Clin Invest. 1973;52:1544–68.
-
(1973)
J Clin Invest
, vol.52
, pp. 1544-1568
-
-
Goldstein, J.L.1
Schrott, H.G.2
Hazzard, W.R.3
Bierman, E.L.4
Motulsky, A.G.5
-
44
-
-
84856235603
-
Management of familial hypercholesterolemia during pregnancy: Case series and discussion
-
PID: 22264579
-
Eapen DJ, Valiani K, Reddy S, Sperling L. Management of familial hypercholesterolemia during pregnancy: case series and discussion. J Clin Lipidol. 2011;6:88–91.
-
(2011)
J Clin Lipidol
, vol.6
, pp. 88-91
-
-
Eapen, D.J.1
Valiani, K.2
Reddy, S.3
Sperling, L.4
-
45
-
-
33750978670
-
Marked changes in plasma lipids and lipoproteins during pregnancy in women with familial hypercholesterolemia
-
Amunsen AL, Khoury J, Iversen PO, Bergei C, Ose L, Tonstad S, et al. Marked changes in plasma lipids and lipoproteins during pregnancy in women with familial hypercholesterolemia. Atherosclerosis. 2006;189:451–7.
-
(2006)
Atherosclerosis
, vol.189
, pp. 451-457
-
-
Amunsen, A.L.1
Khoury, J.2
Iversen, P.O.3
Bergei, C.4
Ose, L.5
Tonstad, S.6
-
46
-
-
0029899325
-
Pregnancy related changes in some cardiovascular risk factors
-
COI: 1:STN:280:DyaK283otVShsA%3D%3D, PID: 8677767
-
Berge LN, Arnesen E, Forsdahl A. Pregnancy related changes in some cardiovascular risk factors. Acta Obstet Gynecol Scand. 1996;75:439–42.
-
(1996)
Acta Obstet Gynecol Scand
, vol.75
, pp. 439-442
-
-
Berge, L.N.1
Arnesen, E.2
Forsdahl, A.3
-
47
-
-
77957744393
-
Dilemmas in treatment of women with familial hypercholesterolaemia during pregnancy
-
COI: 1:STN:280:DC%2BC3cjnsFWqtQ%3D%3D, PID: 20739726
-
Kusters DM, Homsma SJM, Hutten BA, Twickler MTB, Avis HJ, van der Post JA, et al. Dilemmas in treatment of women with familial hypercholesterolaemia during pregnancy. Neth J Med. 2010;68:299–303.
-
(2010)
Neth J Med
, vol.68
, pp. 299-303
-
-
Kusters, D.M.1
Homsma, S.J.M.2
Hutten, B.A.3
Twickler, M.T.B.4
Avis, H.J.5
van der Post, J.A.6
-
48
-
-
0023624926
-
Hypertriglyceridemia: A contraindication for use of bile acid binding resins
-
PID: 3618626
-
Crouse JR. Hypertriglyceridemia: a contraindication for use of bile acid binding resins. Am J Med. 1987;83:243–8.
-
(1987)
Am J Med
, vol.83
, pp. 243-248
-
-
Crouse, J.R.1
-
49
-
-
84883204563
-
Inheritance pattern of familial hypercholesterolemia and markers of cardiovascular risk
-
COI: 1:CAS:528:DC%2BC3sXht1aqtrzK, PID: 23833242
-
Kusters DM, Avis HJ, Braamskamp MJ, et al. Inheritance pattern of familial hypercholesterolemia and markers of cardiovascular risk. J Lipid Res. 2013;54:2543–9.
-
(2013)
J Lipid Res
, vol.54
, pp. 2543-2549
-
-
Kusters, D.M.1
Avis, H.J.2
Braamskamp, M.J.3
-
50
-
-
78650352422
-
Dyslipidemia of mothers with familial hypercholesterolemia deteriorates lipids in adult offspring
-
PID: 20864670
-
Van der Graaf A, Vissers MN, Gaudet D, et al. Dyslipidemia of mothers with familial hypercholesterolemia deteriorates lipids in adult offspring. Arterioscler Thromb Vasc Biol. 2010;30:2673–7.
-
(2010)
Arterioscler Thromb Vasc Biol
, vol.30
, pp. 2673-2677
-
-
Van der Graaf, A.1
Vissers, M.N.2
Gaudet, D.3
-
51
-
-
0033539313
-
Influence of maternal hypercholesterolemia during pregnancy on progression of early atherosclerotic lesions in childhood: Fate of Early Lesions in Children (FELIC) study
-
COI: 1:STN:280:DyaK1MvkvV2nsw%3D%3D, PID: 10520631
-
Napoli C, Glass CK, Witztum JL, et al. Influence of maternal hypercholesterolemia during pregnancy on progression of early atherosclerotic lesions in childhood: Fate of Early Lesions in Children (FELIC) study. Lancet. 1999;354:1234–41.
-
(1999)
Lancet
, vol.354
, pp. 1234-1241
-
-
Napoli, C.1
Glass, C.K.2
Witztum, J.L.3
-
52
-
-
77949485460
-
Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familiar hypercholesterolemia: A randomized, double-blind, placebo-controlled trial
-
COI: 1:CAS:528:DC%2BC3cXjs1ait74%3D, PID: 20227758
-
Raal FJ, Santos RD, Blom DJ, et al. Mipomersen, an apolipoprotein B synthesis inhibitor, for lowering of LDL cholesterol concentrations in patients with homozygous familiar hypercholesterolemia: a randomized, double-blind, placebo-controlled trial. Lancet. 2010;375:998–1006.
-
(2010)
Lancet
, vol.375
, pp. 998-1006
-
-
Raal, F.J.1
Santos, R.D.2
Blom, D.J.3
-
53
-
-
84924415690
-
Long-term efficacy and safety of mipomersen in patients with familial hypercholesterolemia: 2-year interim results of an open-label extension
-
Santos RD, Duell PB, East C, et al. Long-term efficacy and safety of mipomersen in patients with familial hypercholesterolemia: 2-year interim results of an open-label extension. Eur Heart J. 2013. doi:10.1093/eurheart/eht549.
-
(2013)
Eur Heart J
-
-
Santos, R.D.1
Duell, P.B.2
East, C.3
-
54
-
-
84871945617
-
Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolemia: A single-arm, open-label, phase 3 study
-
COI: 1:CAS:528:DC%2BC38Xhs1ajsb%2FM, PID: 23122768
-
Cuchel M, Meagher EA, du Toit Theron H, et al. Efficacy and safety of a microsomal triglyceride transfer protein inhibitor in patients with homozygous familial hypercholesterolemia: a single-arm, open-label, phase 3 study. Lancet. 2013;381:40–6.
-
(2013)
Lancet
, vol.381
, pp. 40-46
-
-
Cuchel, M.1
Meagher, E.A.2
du Toit Theron, H.3
|