-
1
-
-
84921911133
-
Familial hypercholesterolemia-epidemiology, diagnosis, and screening
-
Singh, S., and V. Bittner. 2015. Familial hypercholesterolemia-epidemiology, diagnosis, and screening. Curr. Atheroscler. Rep. 17:482-485.
-
(2015)
Curr. Atheroscler. Rep.
, vol.17
, pp. 482-485
-
-
Singh, S.1
Bittner, V.2
-
2
-
-
84949955967
-
Familial hypercholesterolemia: A review of the natural history, diagnosis, and management
-
Najam, O., and K. Ray. 2015. Familial hypercholesterolemia: a review of the natural history, diagnosis, and management. Cardiol. Ther. 4:25-38.
-
(2015)
Cardiol. Ther.
, vol.4
, pp. 25-38
-
-
Najam, O.1
Ray, K.2
-
3
-
-
84966551189
-
Mutations causative of familial hypercholesterolaemia: Screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217
-
Benn, M., G. Watts, A. Tybjarg-Hansen, and B. Nordestgaard. 2016. Mutations causative of familial hypercholesterolaemia: screening of 98 098 individuals from the Copenhagen General Population Study estimated a prevalence of 1 in 217. Eur. Heart J. 37:1384-1394.
-
(2016)
Eur. Heart J.
, vol.37
, pp. 1384-1394
-
-
Benn, M.1
Watts, G.2
Tybjarg-Hansen, A.3
Nordestgaard, B.4
-
4
-
-
84962489955
-
Mutational analysis of a cohort with clinical diagnosis of familial hypercholesterolemia: Considerations for genetic diagnosis improvement
-
Medeiros, A., A. Alves, and M. Bourbon. 2016. Mutational analysis of a cohort with clinical diagnosis of familial hypercholesterolemia: considerations for genetic diagnosis improvement. Genet. Med. 18:316-324.
-
(2016)
Genet. Med.
, vol.18
, pp. 316-324
-
-
Medeiros, A.1
Alves, A.2
Bourbon, M.3
-
5
-
-
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
-
Nordestgaard, B., M. Chapman, S. Humphries, H. Ginsberg, L. Masana, O. Descamps, O. Wiklund, R. Hegele, F. Raal, J. Defesche, et al. 2013. 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. 34:3478-3490a.
-
(2013)
Eur. Heart J.
, vol.34
, pp. 3478-3490a
-
-
Nordestgaard, B.1
Chapman, M.2
Humphries, S.3
Ginsberg, H.4
Masana, L.5
Descamps, O.6
Wiklund, O.7
Hegele, R.8
Raal, F.9
Defesche, J.10
-
6
-
-
84878528941
-
Management of familial heterozygous hypercholesterolemia: Position Paper of the Polish Lipid Expert Forum
-
Rynkiewicz, A., B. Cybulska, M. Banach, K. Filipiak, T. Guzik, B. Idzior-Walu., J. Imiela, P. Jankowski, L. Kosiewicz-Latoszek, J. Limon, et al. 2013. Management of familial heterozygous hypercholesterolemia: Position Paper of the Polish Lipid Expert Forum. J. Clin. Lipidol. 7:217-221.
-
(2013)
J. Clin. Lipidol.
, vol.7
, pp. 217-221
-
-
Rynkiewicz, A.1
Cybulska, B.2
Banach, M.3
Filipiak, K.4
Guzik, T.5
Idzior-Walu, B.6
Imiela, J.7
Jankowski, P.8
Kosiewicz-Latoszek, L.9
Limon, J.10
-
7
-
-
84870847595
-
Severe familial hypercholesterolaemia: Current and future management
-
Farnier, M., and E. Bruckert. 2012. Severe familial hypercholesterolaemia: current and future management. Arch. Cardiovasc. Dis. 105:656-665.
-
(2012)
Arch. Cardiovasc. Dis.
, vol.105
, pp. 656-665
-
-
Farnier, M.1
Bruckert, E.2
-
8
-
-
84922178425
-
The genetics of familial hypercholesterolemia and emerging therapies
-
Vogt, A. 2015. The genetics of familial hypercholesterolemia and emerging therapies. Appl. Clin. Genet. 8:27-36.
-
(2015)
Appl. Clin. Genet.
, vol.8
, pp. 27-36
-
-
Vogt, A.1
-
9
-
-
84945497118
-
Challenges in the diagnosis and treatment of homozygous familial hypercholesterolemia
-
Ito, M., and G. Watts. 2015. Challenges in the diagnosis and treatment of homozygous familial hypercholesterolemia. Drugs. 75:1715-1724.
-
(2015)
Drugs.
, vol.75
, pp. 1715-1724
-
-
Ito, M.1
Watts, G.2
-
10
-
-
84961226154
-
Homozygous familial hypercholesterolemia: Phenotype rules!
-
Santos, R. 2016. Homozygous familial hypercholesterolemia: phenotype rules! Atherosclerosis. 248:252-254.
-
(2016)
Atherosclerosis.
, vol.248
, pp. 252-254
-
-
Santos, R.1
-
11
-
-
84987757912
-
Progress in the care of familial hypercholesterolemia: 2016
-
Bell, D. A., and G. F. Watts. 2016. Progress in the care of familial hypercholesterolemia: 2016. Med. J. Aust. 205:232-236.
-
(2016)
Med. J. Aust.
, vol.205
, pp. 232-236
-
-
Bell, D.A.1
Watts, G.F.2
-
12
-
-
84893873856
-
Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: A study of a cohort of 14, 000 mutation carriers
-
Besseling, J., I. Kindt, M. Hof, J. Kastelein, B. Hutten, and G. Hovingh. 2014. Severe heterozygous familial hypercholesterolemia and risk for cardiovascular disease: a study of a cohort of 14, 000 mutation carriers. Atherosclerosis. 233:219-223.
-
(2014)
Atherosclerosis.
, vol.233
, pp. 219-223
-
-
Besseling, J.1
Kindt, I.2
Hof, M.3
Kastelein, J.4
Hutten, B.5
Hovingh, G.6
-
13
-
-
0015839023
-
Hyperlipidemia in coronary heart disease I. Lipid levels in 500 survivors of myocardial infarction
-
Goldstein, J., W. Hazzard, H. Schrott, E. Bierman, and A. Motulsky. 1973. Hyperlipidemia in coronary heart disease I. Lipid levels in 500 survivors of myocardial infarction. J. Clin. Invest. 52:1533-1543.
-
(1973)
J. Clin. Invest.
, vol.52
, pp. 1533-1543
-
-
Goldstein, J.1
Hazzard, W.2
Schrott, H.3
Bierman, E.4
Motulsky, A.5
-
14
-
-
84919769680
-
Canadian Cardiovascular Society position statement on familial hypercholesterolemia
-
Genest, J., R. Hegele, J. Bergeron, J. Brophy, A. Carpentier, P. Couture, J. Davignon, R. Dufour, J. Frohlich, D. Gaudet, et al. 2014. Canadian Cardiovascular Society position statement on familial hypercholesterolemia. Can. J. Cardiol. 30:1471-1481.
-
(2014)
Can. J. Cardiol.
, vol.30
, pp. 1471-1481
-
-
Genest, J.1
Hegele, R.2
Bergeron, J.3
Brophy, J.4
Carpentier, A.5
Couture, P.6
Davignon, J.7
Dufour, R.8
Frohlich, J.9
Gaudet, D.10
-
15
-
-
84961851444
-
Prevalence of familial hypercholesterolemia in the 1999 to 2012 United States National Health and Nutrition Examination Surveys (NHANES) clinical perspective
-
de Ferranti, S., A. Rodday, M. Mendelson, J. Wong, L. Leslie, and R. Sheldrick. 2016. Prevalence of familial hypercholesterolemia in the 1999 to 2012 United States National Health and Nutrition Examination Surveys (NHANES) clinical perspective. Circulation. 133:1067-1072.
-
(2016)
Circulation.
, vol.133
, pp. 1067-1072
-
-
De Ferranti, S.1
Rodday, A.2
Mendelson, M.3
Wong, J.4
Leslie, L.5
Sheldrick, R.6
-
16
-
-
84961842026
-
Knowing the prevalence of familial hypercholesterolemia matters
-
Goldberg, A., and S. Gidding. 2016. Knowing the prevalence of familial hypercholesterolemia matters. Circulation. 133:1054-1057.
-
(2016)
Circulation.
, vol.133
, pp. 1054-1057
-
-
Goldberg, A.1
Gidding, S.2
-
17
-
-
68049122102
-
Preferred reporting items for systematic reviews and meta-analyses: The PRISMA statement
-
Moher, D., A. Liberati, J. Tetzlaff, and D. Altman. 2009. Preferred Reporting Items for Systematic Reviews and Meta-Analyses: The PRISMA Statement. PLoS Med. 6:e1000097.
-
(2009)
PLoS Med.
, vol.6
, pp. e1000097
-
-
Moher, D.1
Liberati, A.2
Tetzlaff, J.3
Altman, D.4
-
18
-
-
84863524483
-
Uso de ezetimibe en el tratamiento de la hipercolesterolemia
-
Araujo, M., P. Botto, and C. Mazza. 2012. Uso de ezetimibe en el tratamiento de la hipercolesterolemia. An. Pediatr. (Barc.). 77:37-42.
-
(2012)
An. Pediatr. (Barc.).
, vol.77
, pp. 37-42
-
-
Araujo, M.1
Botto, P.2
Mazza, C.3
-
19
-
-
80051647496
-
Severe hypercholesterolemia in children. Presentation of two cases and update of the literature
-
e71
-
Araujo, M. B., M. S. Pacce, M. Bravo, A. M. Pugliese, and C. Mazza. 2011. Severe hypercholesterolemia in children. Presentation of two cases and update of the literature. Arch. Argent. Pediatr. 109:e67. e71.
-
(2011)
Arch. Argent. Pediatr.
, vol.109
, pp. e67
-
-
Araujo, M.B.1
Pacce, M.S.2
Bravo, M.3
Pugliese, A.M.4
Mazza, C.5
-
20
-
-
34548665729
-
Combined cardiohepatic transplantation due to severe heterozygous familial hypercholesteremia type II: First case in Argentina.a case report
-
Ahualli, L., A. Stewart-Harris, G. Bastianelli, D. Radlovachki, A. Bartolome, P. Trigo, N. Cejas, G. Aballay Soteras, F. Duek, J. Lendoire, et al. 2007. Combined cardiohepatic transplantation due to severe heterozygous familial hypercholesteremia type II: first case in Argentina.a case report. Transplant. Proc. 39:2449-2453.
-
(2007)
Transplant. Proc.
, vol.39
, pp. 2449-2453
-
-
Ahualli, L.1
Stewart-Harris, A.2
Bastianelli, G.3
Radlovachki, D.4
Bartolome, A.5
Trigo, P.6
Cejas, N.7
Aballay Soteras, G.8
Duek, F.9
Lendoire, J.10
-
21
-
-
0026439760
-
High frequency of the Lebanese allele of the LDLr gene among Brazilian patients with familial hypercholesterolaemia
-
Figueiredo, M., J. Dos Santos, F. Alberto, and M. Zago. 1992. High frequency of the Lebanese allele of the LDLr gene among Brazilian patients with familial hypercholesterolaemia. J. Med. Genet. 29:813-815.
-
(1992)
J. Med. Genet.
, vol.29
, pp. 813-815
-
-
Figueiredo, M.1
Dos Santos, J.2
Alberto, F.3
Zago, M.4
-
22
-
-
0033144184
-
The Lebanese mutation as an important cause of familial hypercholesterolemia in Brazil
-
Alberto, F., M. Figueiredo, M. Zago, A. Araujo, and J. Dos-Santos. 1999. The Lebanese mutation as an important cause of familial hypercholesterolemia in Brazil. Braz. J. Med. Biol. Res. 32:739-745.
-
(1999)
Braz. J. Med. Biol. Res.
, vol.32
, pp. 739-745
-
-
Alberto, F.1
Figueiredo, M.2
Zago, M.3
Araujo, A.4
Dos-Santos, J.5
-
23
-
-
0037357676
-
Identification of a new mutation, S305C, in exon 7 of the low-density lipoprotein receptor gene in a Brazilian family with homozygous familial hypercholesterolemia
-
van de Kerkhof, L., S. Van Eijk, J. Defesche, and J. Dos-Santos. 2003. Identification of a new mutation, S305C, in exon 7 of the low-density lipoprotein receptor gene in a Brazilian family with homozygous familial hypercholesterolemia. Genet. Test. 7:77-79.
-
(2003)
Genet. Test.
, vol.7
, pp. 77-79
-
-
Van De Kerkhof, L.1
Van Eijk, S.2
Defesche, J.3
Dos-Santos, J.4
-
24
-
-
0036551218
-
Molecular basis of familial hypercholesterolemia in Brazil: Identification of seven novel LDLR gene mutations
-
Salazar, L., M. Hirata, S. Cavalli, E. Nakandakare, N. Forti, J. Diament, S. Giannini, M. Bertolami, and R. Hirata. 2002. Molecular basis of familial hypercholesterolemia in Brazil: identification of seven novel LDLR gene mutations. Hum. Mutat. 19:462-463.
-
(2002)
Hum. Mutat.
, vol.19
, pp. 462-463
-
-
Salazar, L.1
Hirata, M.2
Cavalli, S.3
Nakandakare, E.4
Forti, N.5
Diament, J.6
Giannini, S.7
Bertolami, M.8
Hirata, R.9
-
25
-
-
84878002564
-
Extensive xanthomas and severe subclinical atherosclerosis in homozygous familial hypercholesterolemia
-
Rocha, V., A. Chacra, W. Salgado, M. Miname, L. Turolla, A. Gagliardi, E. Ribeiro, R. Rocha, L. Avila, A. Pereira, et al. 2013. Extensive xanthomas and severe subclinical atherosclerosis in homozygous familial hypercholesterolemia. J. Am. Coll. Cardiol. 61:2193.
-
(2013)
J. Am. Coll. Cardiol.
, vol.61
, pp. 2193
-
-
Rocha, V.1
Chacra, A.2
Salgado, W.3
Miname, M.4
Turolla, L.5
Gagliardi, A.6
Ribeiro, E.7
Rocha, R.8
Avila, L.9
Pereira, A.10
-
26
-
-
85002818767
-
A case of severe carotid stenosis in a patient with familial hypercholesterolemia without significant coronary artery disease
-
Barros, M., H. Ferreira-Fernandes, I. Barros, A. Barbosa, and G. Pinto. 2014. A case of severe carotid stenosis in a patient with familial hypercholesterolemia without significant coronary artery disease. Case Rep. Cardiol. 2014:853921.
-
(2014)
Case Rep. Cardiol.
, vol.2014
, pp. 853921
-
-
Barros, M.1
Ferreira-Fernandes, H.2
Barros, I.3
Barbosa, A.4
Pinto, G.5
-
27
-
-
84913582633
-
Familial hypercholesterolemia in Brazil: Cascade screening program, clinical and genetic aspects
-
Jannes, C., R. Santos, P. de Souza Silva, L. Turolla, A. Gagliardi, J. Marsiglia, A. Chacra, M. Miname, V. Rocha, W. Filho, et al. 2015. Familial hypercholesterolemia in Brazil: cascade screening program, clinical and genetic aspects. Atherosclerosis. 238:101-107.
-
(2015)
Atherosclerosis.
, vol.238
, pp. 101-107
-
-
Jannes, C.1
Santos, R.2
De Souza Silva, P.3
Turolla, L.4
Gagliardi, A.5
Marsiglia, J.6
Chacra, A.7
Miname, M.8
Rocha, V.9
Filho, W.10
-
28
-
-
84908140315
-
What are we able to achieve today for our patients with homozygous familial hypercholesterolaemia, and what are the unmet needs?
-
Santos, R. 2014. What are we able to achieve today for our patients with homozygous familial hypercholesterolaemia, and what are the unmet needs? Atheroscler. Suppl. 15:19-25.
-
(2014)
Atheroscler. Suppl.
, vol.15
, pp. 19-25
-
-
Santos, R.1
-
29
-
-
84906960242
-
Association of peripheral arterial and cardiovascular diseases in familial hypercholesterolemia
-
Pereira, C., M. Miname, M. Makdisse, R. Kalil Filho, and R. Santos. 2014. Association of peripheral arterial and cardiovascular diseases in familial hypercholesterolemia. Arq. Bras. Cardiol. 103:118-123.
-
(2014)
Arq. Bras. Cardiol.
, vol.103
, pp. 118-123
-
-
Pereira, C.1
Miname, M.2
Makdisse, M.3
Kalil Filho, R.4
Santos, R.5
-
30
-
-
84884577104
-
First Brazilian guidelines for familial hypercholesterolemia
-
Santos, R., A. Gagliardi, H. Xavier, A. Casella Filho, D. Araujo, F. Cesena, R. Alves, A. Pereira, A. Lottemberg, A. Chacra, et al. 2012. First Brazilian guidelines for familial hypercholesterolemia. Arq. Bras. Cardiol. 99:1-28.
-
(2012)
Arq. Bras. Cardiol.
, vol.99
, pp. 1-28
-
-
Santos, R.1
Gagliardi, A.2
Xavier, H.3
Casella Filho, A.4
Araujo, D.5
Cesena, F.6
Alves, R.7
Pereira, A.8
Lottemberg, A.9
Chacra, A.10
-
31
-
-
33947592022
-
Hipercolesterolemia familiar heterocigota: Diagnostico molecular y terapia combinada
-
Spanish
-
Arteaga, Ll. A., M. A. Cuevas, R. A. Rigotti, F. Gonzalez, S. Castillo, L. P. Mata, and K. R. Alonso. 2007. Hipercolesterolemia familiar heterocigota: diagnostico molecular y terapia combinada. Caso clinico. Rev. Med. Chil. 135:216-220. Spanish.
-
(2007)
Caso Clinico. Rev. Med. Chil.
, vol.135
, pp. 216-220
-
-
Arteaga, L.A.1
Cuevas, M.A.2
Rigotti, R.A.3
Gonzalez, F.4
Castillo, S.5
Mata, L.P.6
Alonso, K.R.7
-
32
-
-
83355173945
-
Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis
-
Huijgen, R., A. Stork, J. Defeschea, J. Petera, R. Alonso, A. Cuevas, J. Kastelein, M. Durand, and E. Stroes. 2012. Extreme xanthomatosis in patients with both familial hypercholesterolemia and cerebrotendinous xanthomatosis. Clin. Genet. 81:24-28.
-
(2012)
Clin. Genet.
, vol.81
, pp. 24-28
-
-
Huijgen, R.1
Stork, A.2
Defeschea, J.3
Petera, J.4
Alonso, R.5
Cuevas, A.6
Kastelein, J.7
Durand, M.8
Stroes, E.9
-
33
-
-
0031418996
-
Novel stop mutation causing familial hypercholesterolemia in a Costa Rican family
-
Thiart, R., O. Loubser, J. de Villiers, M. Santos, and M. Kotze. 1997. Novel stop mutation causing familial hypercholesterolemia in a Costa Rican family. Mol. Cell. Probes. 11:457-458.
-
(1997)
Mol. Cell. Probes.
, vol.11
, pp. 457-458
-
-
Thiart, R.1
Loubser, O.2
De Villiers, J.3
Santos, M.4
Kotze, M.5
-
34
-
-
0029837815
-
Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor gene
-
Kotze, M., R. Thiart, O. Loubser, J. de Villiers, M. Santos, M. Vargas, and A. Peeters. 1996. Mutation analysis reveals an insertional hotspot in exon 4 of the LDL receptor gene. Hum. Genet. 98:476-478.
-
(1996)
Hum. Genet.
, vol.98
, pp. 476-478
-
-
Kotze, M.1
Thiart, R.2
Loubser, O.3
De Villiers, J.4
Santos, M.5
Vargas, M.6
Peeters, A.7
-
35
-
-
0029082090
-
Recurrent and novel LDL receptor gene mutations causing heterozygous familial hypercholesterolemia in La Habana
-
Pereira, E., R. Ferreira, B. Hermelin, G. Thomas, C. Bernard, V. Bertrand, H. Nassiff, D. Del Castillo, G. Bereziat, and P. Benlian. 1995. Recurrent and novel LDL receptor gene mutations causing heterozygous familial hypercholesterolemia in La Habana. Hum. Genet. 96:319-322.
-
(1995)
Hum. Genet.
, vol.96
, pp. 319-322
-
-
Pereira, E.1
Ferreira, R.2
Hermelin, B.3
Thomas, G.4
Bernard, C.5
Bertrand, V.6
Nassiff, H.7
Del Castillo, D.8
Bereziat, G.9
Benlian, P.10
-
36
-
-
0032803444
-
Familial hypercholesterolemia. Acceptor splice site (G-C) mutation in intron 7 of the LDL-R gene: Alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R (Honduras-1) [LDL-R1061 (-1) G-C]
-
Yu, L., E. Heere-Ress, B. Boucher, J. Defesche, J. Kastelein, M. Lavoie, and J. Genest, Jr. 1999. Familial hypercholesterolemia. Acceptor splice site (G-C) mutation in intron 7 of the LDL-R gene: alternate RNA editing causes exon 8 skipping or a premature stop codon in exon 8. LDL-R (Honduras-1) [LDL-R1061 (-1) G-C]. Atherosclerosis. 146:125-131.
-
(1999)
Atherosclerosis.
, vol.146
, pp. 125-131
-
-
Yu, L.1
Heere-Ress, E.2
Boucher, B.3
Defesche, J.4
Kastelein, J.5
Lavoie, M.6
Genest, J.7
-
37
-
-
19944430011
-
A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia
-
Canizales-Quinteros, S., C. Aguilar-Salinas, A. Huertas-Vazquez, M. Ordonez-Sanchez, M. Rodriguez-Torres, J. Venturas-Gallegos, L. Riba, S. Ramirez-Jimenez, R. Salas-Montiel, G. Medina-Palacios, et al. 2005. A novel ARH splice site mutation in a Mexican kindred with autosomal recessive hypercholesterolemia. Hum. Genet. 116:114-120.
-
(2005)
Hum. Genet.
, vol.116
, pp. 114-120
-
-
Canizales-Quinteros, S.1
Aguilar-Salinas, C.2
Huertas-Vazquez, A.3
Ordonez-Sanchez, M.4
Rodriguez-Torres, M.5
Venturas-Gallegos, J.6
Riba, L.7
Ramirez-Jimenez, S.8
Salas-Montiel, R.9
Medina-Palacios, G.10
-
38
-
-
83655192548
-
Hipercolesterolemia familiar homocigota por la mutacion c2271delT del gen del receptor LDL, detectada unicamente en mexicanos
-
Martinez, L., M. Ordonez Sanchez, R. Letona, V. Olvera Sumano, M. Miguel Guerra, M. Tusie-Luna, and C. Aguilar-Salinas. 2011. Hipercolesterolemia familiar homocigota por la mutacion c2271delT del gen del receptor LDL, detectada unicamente en mexicanos. Gac. Med. Mex. 147:525-527.
-
(2011)
Gac. Med. Mex.
, vol.147
, pp. 525-527
-
-
Martinez, L.1
Ordonez Sanchez, M.2
Letona, R.3
Olvera Sumano, V.4
Miguel Guerra, M.5
Tusie-Luna, M.6
Aguilar-Salinas, C.7
-
39
-
-
84908897549
-
Homozygous familial hypercholesterolemia: The c.1055G>A mutation in the LDLR gene and clinical heterogeneity
-
Magana Torres, M., S. Mora-Hernandez, N. Vazquez Cardenas, and A. Gonzalez Jaimes. 2014. Homozygous familial hypercholesterolemia: the c.1055G>A mutation in the LDLR gene and clinical heterogeneity. J. Clin. Lipidol. 8:525-527.
-
(2014)
J. Clin. Lipidol.
, vol.8
, pp. 525-527
-
-
Magana Torres, M.1
Mora-Hernandez, S.2
Vazquez Cardenas, N.3
Gonzalez Jaimes, A.4
-
40
-
-
80053224510
-
Mutational analysis of the LDL receptor and APOB genes in Mexican individuals with autosomal dominant hypercholesterolemia
-
Vaca, G., A. Vazquez, M. Magana, M. Ramirez, I. Davalos, E. Martinez, B. Marin, and G. Carrillo. 2011. Mutational analysis of the LDL receptor and APOB genes in Mexican individuals with autosomal dominant hypercholesterolemia. Atherosclerosis. 218:391-396.
-
(2011)
Atherosclerosis.
, vol.218
, pp. 391-396
-
-
Vaca, G.1
Vazquez, A.2
Magana, M.3
Ramirez, M.4
Davalos, I.5
Martinez, E.6
Marin, B.7
Carrillo, G.8
-
41
-
-
0034908136
-
Familial Hypercholesterolemia
-
Aguilar-Salinas, C. 2001. Familial Hypercholesterolemia. Rev. Invest. Clin. 53:254-265.
-
(2001)
Rev. Invest. Clin.
, vol.53
, pp. 254-265
-
-
Aguilar-Salinas, C.1
-
42
-
-
28444475924
-
Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico
-
Robles-Osorio, L., A. Huerta-Zepeda, M. L. Ordonez, S. Canizales-Quinteros, A. Diaz-Villasenor, R. Gutierrez-Aguilar, L. Riba, A. Huertas-Vazquez, M. Rodriguez-Torres, R. A. Gomez-Diaz, et al. 2006. Genetic heterogeneity of autosomal dominant hypercholesterolemia in Mexico. Arch. Med. Res. 37:102-108.
-
(2006)
Arch. Med. Res.
, vol.37
, pp. 102-108
-
-
Robles-Osorio, L.1
Huerta-Zepeda, A.2
Ordonez, M.L.3
Canizales-Quinteros, S.4
Diaz-Villasenor, A.5
Gutierrez-Aguilar, R.6
Riba, L.7
Huertas-Vazquez, A.8
Rodriguez-Torres, M.9
Gomez-Diaz, R.A.10
-
43
-
-
0037279865
-
Familial hypercholesterolemia due to liganddefective apolipoprotein B100: First case report in a Mexican family
-
Robles-Osorio, L., M. L. Ordonez, C. A. Aguilar-Salinas, M. Auron-Gomez, M. T. Tusie-Luna, F. J. Gomez-Perez, and J. A. Rull-Rodrigo. 2003. Familial hypercholesterolemia due to liganddefective apolipoprotein B100: first case report in a Mexican family. Arch. Med. Res. 34:70-75.
-
(2003)
Arch. Med. Res.
, vol.34
, pp. 70-75
-
-
Robles-Osorio, L.1
Ordonez, M.L.2
Aguilar-Salinas, C.A.3
Auron-Gomez, M.4
Tusie-Luna, M.T.5
Gomez-Perez, F.J.6
Rull-Rodrigo, J.A.7
-
44
-
-
79952367369
-
Visual vignette. Familial hypercholesterolemia
-
Burgos, A., M. Aguilar, and K. de Arias. 2011. Visual vignette. Familial hypercholesterolemia. Endocr. Pract. 17:154.
-
(2011)
Endocr. Pract.
, vol.17
, pp. 154
-
-
Burgos, A.1
Aguilar, M.2
De Arias, K.3
-
45
-
-
33644940875
-
Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent
-
Cefalu, A., G. Barraco, D. Noto, V. Valenti, C. Barbagallo, G. Elisir, L. Cuniberti, J. Werba, M. Libra, S. Costa, et al. 2006. Six novel mutations of the LDL receptor gene in FH kindred of Sicilian and Paraguayan descent. Int. J. Mol. Med. 17:539-546.
-
(2006)
Int. J. Mol. Med.
, vol.17
, pp. 539-546
-
-
Cefalu, A.1
Barraco, G.2
Noto, D.3
Valenti, V.4
Barbagallo, C.5
Elisir, G.6
Cuniberti, L.7
Werba, J.8
Libra, M.9
Costa, S.10
-
46
-
-
65449165959
-
Una nueva mutacion en el promotor del gen del receptor de las lipoproteinas de baja densidad asociada a hipercolesterolemia familiar en homocigosis y heterocigosis
-
Esperon, P., V. Raggio, and M. Stoll. 2009. Una nueva mutacion en el promotor del gen del receptor de las lipoproteinas de baja densidad asociada a hipercolesterolemia familiar en homocigosis y heterocigosis. Clin. Investig. Arterioscler. 21:51-55.
-
(2009)
Clin. Investig. Arterioscler.
, vol.21
, pp. 51-55
-
-
Esperon, P.1
Raggio, V.2
Stoll, M.3
-
47
-
-
85002676416
-
Previniendo el infarto en el adulto joven: GENYCO, un registro nacional de hipercolesterolemia familiar
-
Stoll, M., M. Lorenzo, V. Raggio, P. Esperon, and M. Zelarayan. 2011. Previniendo el infarto en el adulto joven: GENYCO, un registro nacional de hipercolesterolemia familiar. Revista Uruguaya Cardiologia. 26:16-26.
-
(2011)
Revista Uruguaya Cardiologia.
, vol.26
, pp. 16-26
-
-
Stoll, M.1
Lorenzo, M.2
Raggio, V.3
Esperon, P.4
Zelarayan, M.5
-
48
-
-
85002894212
-
Mutacion en el gen de la apolipoproteina B responsable de hipercolesterolemia familiar: Primeros dos casos clinicos reportados en Uruguay
-
Esperon, P., V. Raggio, M. Lorenzo, and M. Stoll. 2013. Mutacion en el gen de la apolipoproteina B responsable de hipercolesterolemia familiar: primeros dos casos clinicos reportados en Uruguay. Revista Uruguaya de Cardiologia. 28:182-188.
-
(2013)
Revista Uruguaya de Cardiologia.
, vol.28
, pp. 182-188
-
-
Esperon, P.1
Raggio, V.2
Lorenzo, M.3
Stoll, M.4
-
49
-
-
0027026881
-
Molecular genetics of the LDL receptor gene in familial hypercholesterolemia
-
Hobbs, H., M. Brown, and J. Goldstein. 1992. Molecular genetics of the LDL receptor gene in familial hypercholesterolemia. Hum. Mutat. 1:445-466.
-
(1992)
Hum. Mutat.
, vol.1
, pp. 445-466
-
-
Hobbs, H.1
Brown, M.2
Goldstein, J.3
-
50
-
-
0033044612
-
Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia
-
Bertolini, S., S. Cassanelli, R. Garuti, M. Ghisellini, M. Simone, M. Rolleri, P. Masturzo, and S. Calandra. 1999. Analysis of LDL receptor gene mutations in Italian patients with homozygous familial hypercholesterolemia. Arterioscler. Thromb. Vasc. Biol. 19:408-418.
-
(1999)
Arterioscler. Thromb. Vasc. Biol.
, vol.19
, pp. 408-418
-
-
Bertolini, S.1
Cassanelli, S.2
Garuti, R.3
Ghisellini, M.4
Simone, M.5
Rolleri, M.6
Masturzo, P.7
Calandra, S.8
-
51
-
-
0032248337
-
Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia
-
Cenarro, A., H. Jensen, E. Casao, F. Civeira, J. Gonzalez-Bonillo, J. Rodriguez-Rey, N. Gregersen, and M. Pocovi. 1998. Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia. Hum. Mutat. 11:413.
-
(1998)
Hum. Mutat.
, vol.11
, pp. 413
-
-
Cenarro, A.1
Jensen, H.2
Casao, E.3
Civeira, F.4
Gonzalez-Bonillo, J.5
Rodriguez-Rey, J.6
Gregersen, N.7
Pocovi, M.8
-
52
-
-
0024446716
-
Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners
-
Leitersdorf, E., D. Van der Westhuyzen, G. Coetzee, and H. Hobbs. 1989. Two common low density lipoprotein receptor gene mutations cause familial hypercholesterolemia in Afrikaners. J. Clin. Invest. 84:954-961.
-
(1989)
J. Clin. Invest.
, vol.84
, pp. 954-961
-
-
Leitersdorf, E.1
Van Der Westhuyzen, D.2
Coetzee, G.3
Hobbs, H.4
-
53
-
-
0036889631
-
Molecular genetic analysis of familial hypercholesterolemia: Spectrum and regional difference of LDL receptor gene mutations in Japanese population
-
Yu, W., A. Nohara, T. Higashikata, H. Lu, A. Inazu, and H. Mabuchi. 2002. Molecular genetic analysis of familial hypercholesterolemia: spectrum and regional difference of LDL receptor gene mutations in Japanese population. Atherosclerosis. 165:335-342.
-
(2002)
Atherosclerosis.
, vol.165
, pp. 335-342
-
-
Yu, W.1
Nohara, A.2
Higashikata, T.3
Lu, H.4
Inazu, A.5
Mabuchi, H.6
-
54
-
-
0021742599
-
The human LDL receptor: A cysteinerich protein with multiple Alu sequences in its mRNA
-
Yamamoto, T., C. Davis, M. Brown, W. Schneider, M. Casey, J. Goldstein, and D. Russell. 1984. The human LDL receptor: a cysteinerich protein with multiple Alu sequences in its mRNA. Cell. 39:27-38.
-
(1984)
Cell.
, vol.39
, pp. 27-38
-
-
Yamamoto, T.1
Davis, C.2
Brown, M.3
Schneider, W.4
Casey, M.5
Goldstein, J.6
Russell, D.7
-
55
-
-
1242341458
-
Familial hypercholesterolemia in Brazil
-
Dos Santos, J. 2003. Familial hypercholesterolemia in Brazil. Atheroscler. Suppl. 4:1-2.
-
(2003)
Atheroscler. Suppl.
, vol.4
, pp. 1-2
-
-
Dos Santos, J.1
-
56
-
-
0242416622
-
Molecular mechanisms of autosomal recessive hypercholesterolemia
-
Cohen, J., M. Kimmel, A. Polanski, and H. Hobbs. 2003. Molecular mechanisms of autosomal recessive hypercholesterolemia. Curr. Opin. Lipidol. 14:121-127.
-
(2003)
Curr. Opin. Lipidol.
, vol.14
, pp. 121-127
-
-
Cohen, J.1
Kimmel, M.2
Polanski, A.3
Hobbs, H.4
-
57
-
-
18244365633
-
Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene
-
Bednarska-Makaruk, M., M. Bisko, M. Puawska, D. Hoffman-Zacharska, M. Rodo, M. Roszczynko, A. Solik-Tomassi, G. Broda, M. Polakowska, A. Pytlak, et al. 2001. Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene. Eur. J. Hum. Genet. 9:836-842.
-
(2001)
Eur. J. Hum. Genet.
, vol.9
, pp. 836-842
-
-
Bednarska-Makaruk, M.1
Bisko, M.2
Puawska, M.3
Hoffman-Zacharska, D.4
Rodo, M.5
Roszczynko, M.6
Solik-Tomassi, A.7
Broda, G.8
Polakowska, M.9
Pytlak, A.10
-
58
-
-
84857035544
-
Molecular characterization of familial hypercholesterolemia in Spain
-
Palacios, L., L. Grandoso, N. Cuevas, E. Olano-Martin, A. Martinez, D. Tejedor, and M. Stef. 2012. Molecular characterization of familial hypercholesterolemia in Spain. Atherosclerosis. 221:137-142.
-
(2012)
Atherosclerosis.
, vol.221
, pp. 137-142
-
-
Palacios, L.1
Grandoso, L.2
Cuevas, N.3
Olano-Martin, E.4
Martinez, A.5
Tejedor, D.6
Stef, M.7
-
59
-
-
84873929361
-
Low prevalence of mutations in known loci for autosomal dominant hypercholesterolemia in a multiethnic patient cohort
-
Ahmad, Z., B. Adams-Huet, C. Chen, and A. Garg. 2012. Low prevalence of mutations in known loci for autosomal dominant hypercholesterolemia in a multiethnic patient cohort. Circ Cardiovasc Genet. 5:666-675.
-
(2012)
Circ Cardiovasc Genet.
, vol.5
, pp. 666-675
-
-
Ahmad, Z.1
Adams-Huet, B.2
Chen, C.3
Garg, A.4
-
60
-
-
79951550993
-
National, regional, and global trends in serum total cholesterol since 1980: Systematic analysis of health examination surveys and epidemiological studies with 321 country-years and 3'0 million participants
-
Farzadfar, F., M. Finucane, G. Danaei, P. Pelizzari, M. Cowan, C. Paciorek, G. Singh, J. Lin, G. Stevens, L. Riley, et al. 2011. National, regional, and global trends in serum total cholesterol since 1980: systematic analysis of health examination surveys and epidemiological studies with 321 country-years and 3'0 million participants. Lancet. 377:578-586.
-
(2011)
Lancet.
, vol.377
, pp. 578-586
-
-
Farzadfar, F.1
Finucane, M.2
Danaei, G.3
Pelizzari, P.4
Cowan, M.5
Paciorek, C.6
Singh, G.7
Lin, J.8
Stevens, G.9
Riley, L.10
-
61
-
-
84950321185
-
Reflections on the conceptualization and measurement of access to health services in Argentina: The case of the National Survey of Risk Factors 2009
-
Ballesteros, M. S., and B. Freidin. 2015. Reflections on the conceptualization and measurement of access to health services in Argentina: the case of the National Survey of Risk Factors 2009. Salud Colect. 11:523-535.
-
(2015)
Salud Colect.
, vol.11
, pp. 523-535
-
-
Ballesteros, M.S.1
Freidin, B.2
-
62
-
-
84961253120
-
Risk and protective factors for chronic diseases by telephone survey in capitals of Brazil, Vigitel 2014
-
Malta, D. C., S. R. Stopa, B. P. Iser, R. T. Bernal, R. M. Claro, A. C. Nardi, A. A. Dos Reis, and C. A. Monteiro. 2015. Risk and protective factors for chronic diseases by telephone survey in capitals of Brazil, Vigitel 2014. Rev. Bras. Epidemiol. 18(Suppl 2):238-255.
-
(2015)
Rev. Bras. Epidemiol.
, vol.18
, pp. 238-255
-
-
Malta, D.C.1
Stopa, S.R.2
Iser, B.P.3
Bernal, R.T.4
Claro, R.M.5
Nardi, A.C.6
Dos Reis, A.A.7
Monteiro, C.A.8
-
63
-
-
84958260552
-
Prevalence, awareness, treatment, and control of high low-density lipoprotein cholesterol in Brazil: Baseline of the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil)
-
Lotufo, P., R. Santos, R. Figueiredo, A. Pereira, J. Mill, S. Alvim, M. Fonseca, M. Almeida, M. Molina, D. Chor, et al. 2016. Prevalence, awareness, treatment, and control of high low-density lipoprotein cholesterol in Brazil: Baseline of the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil). J. Clin. Lipidol. 10:568-576.
-
(2016)
J. Clin. Lipidol.
, vol.10
, pp. 568-576
-
-
Lotufo, P.1
Santos, R.2
Figueiredo, R.3
Pereira, A.4
Mill, J.5
Alvim, S.6
Fonseca, M.7
Almeida, M.8
Molina, M.9
Chor, D.10
-
64
-
-
84964694396
-
The National Health Survey of Chile gives useful information to health policy planning: Analysis of diabetic nephropathy as an index of potential saving
-
Cabrera, S., M. Alvo, J. S. Mindell, and C. Ferro. 2015. The National Health Survey of Chile gives useful information to health policy planning: analysis of diabetic nephropathy as an index of potential saving. Rev. Med. Chil. 143:679-681.
-
(2015)
Rev. Med. Chil.
, vol.143
, pp. 679-681
-
-
Cabrera, S.1
Alvo, M.2
Mindell, J.S.3
Ferro, C.4
-
65
-
-
84945474198
-
Ecuador's National Health and Nutrition Survey: Objectives, design, and methods
-
Freire, W. B., P. Belmont, D. F. López-Cevallos, and W. Waters. 2015. Ecuador's National Health and Nutrition Survey: objectives, design, and methods. Ann. Epidemiol. 25:877-878.
-
(2015)
Ann. Epidemiol.
, vol.25
, pp. 877-878
-
-
Freire, W.B.1
Belmont, P.2
López-Cevallos, D.F.3
Waters, W.4
-
66
-
-
84881503207
-
Type 2 diabetes and frequency of prevention and control measures
-
Jiménez-Corona, A., C. A. Aguilar-Salinas, R. Rojas-Martínez, and M. Hernández-Ávila. 2013. Type 2 diabetes and frequency of prevention and control measures. Salud Publica Mex. 55(Suppl 2):S137-S143.
-
(2013)
Salud Publica Mex.
, vol.55
, pp. S137-S143
-
-
Jiménez-Corona, A.1
Aguilar-Salinas, C.A.2
Rojas-Martínez, R.3
Hernández-Ávila, M.4
-
67
-
-
78349296834
-
Prevalence of dyslipidemias in the Mexican National Health and Nutrition Survey 2006
-
Aguilar-Salinas, C., F. Gómez-Pérez, J. Rull, S. Villalpando, S. Barquera, and R. Rojas. 2010. Prevalence of dyslipidemias in the Mexican National Health and Nutrition Survey 2006. Salud Publica Mex. 52:S44-S53.
-
(2010)
Salud Publica Mex.
, vol.52
, pp. S44-S53
-
-
Aguilar-Salinas, C.1
Gómez-Pérez, F.2
Rull, J.3
Villalpando, S.4
Barquera, S.5
Rojas, R.6
-
68
-
-
78349289673
-
Prevention of cardiovascular disease based on lipid lowering treatment: A challenge for the Mexican health system
-
Gómez-Pérez, F., R. Rojas, S. Villalpando, S. Barquera, J. Rull, and C. Aguilar-Salinas. 2010. Prevention of cardiovascular disease based on lipid lowering treatment: a challenge for the Mexican health system. Salud Publica Mex. 52(Suppl 1):S54-S62.
-
(2010)
Salud Publica Mex.
, vol.52
, pp. S54-S62
-
-
Gómez-Pérez, F.1
Rojas, R.2
Villalpando, S.3
Barquera, S.4
Rull, J.5
Aguilar-Salinas, C.6
-
69
-
-
84969596203
-
Diagnostic yield and clinical utility of sequencing familial hypercholesterolemia genes in patients with severe hypercholesterolemia
-
Khera, A., H. Won, G. Peloso, K. Lawson, T. Bartz, X. Deng, E. van Leeuwen, P. Natarajan, C. Emdin, A. Bick, et al. 2016. Diagnostic yield and clinical utility of sequencing familial hypercholesterolemia genes in patients with severe hypercholesterolemia. J. Am. Coll. Cardiol. 67:2578-2589.
-
(2016)
J. Am. Coll. Cardiol.
, vol.67
, pp. 2578-2589
-
-
Khera, A.1
Won, H.2
Peloso, G.3
Lawson, K.4
Bartz, T.5
Deng, X.6
Van Leeuwen, E.7
Natarajan, P.8
Emdin, C.9
Bick, A.10
-
70
-
-
0022571020
-
Causes of death in patients with familial hypercholesterolemia
-
Mabuchi, H., S. Miyamoto, K. Ueda, M. Oota, T. Takegoshi, T. Wakasugi, and R. Takeda. 1986. Causes of death in patients with familial hypercholesterolemia. Atherosclerosis. 61:1-6.
-
(1986)
Atherosclerosis.
, vol.61
, pp. 1-6
-
-
Mabuchi, H.1
Miyamoto, S.2
Ueda, K.3
Oota, M.4
Takegoshi, T.5
Wakasugi, T.6
Takeda, R.7
-
71
-
-
0025944056
-
Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group
-
1991. Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. BMJ. 303:893-896.
-
(1991)
BMJ.
, vol.303
, pp. 893-896
-
-
-
72
-
-
0842309234
-
Cardiovascular disease and mortality in statin-treated patients with familial hypercholesterolemia
-
Mohrschladt, M., R. Westendorp, J. Gevers Leuven, and A. Smelt. 2004. Cardiovascular disease and mortality in statin-treated patients with familial hypercholesterolemia. Atherosclerosis. 172:329-335.
-
(2004)
Atherosclerosis.
, vol.172
, pp. 329-335
-
-
Mohrschladt, M.1
Westendorp, R.2
Gevers Leuven, J.3
Smelt, A.4
-
73
-
-
84931028781
-
Mortality among patients with familial hypercholesterolemia: A registry-based study in Norway, 1992-2010
-
Mundal, L., M. Sarancic, L. Ose, P. Iversen, J. Borgan, M. Veierod, T. Leren, and K. Retterstol. 2014. Mortality among patients with familial hypercholesterolemia: a registry-based study in Norway, 1992-2010. J. Am. Heart Assoc. 3:e001236.
-
(2014)
J. Am. Heart Assoc.
, vol.3
, pp. e001236
-
-
Mundal, L.1
Sarancic, M.2
Ose, L.3
Iversen, P.4
Borgan, J.5
Veierod, M.6
Leren, T.7
Retterstol, K.8
-
74
-
-
79958166529
-
Clinical characteristics and evaluation of LDL-cholesterol treatment of the Spanish Familial Hypercholesterolemia Longitudinal Cohort Study (SAFEHEART)
-
Mata, N., R. Alonso, L. Badimón, T. Padró, F. Fuentes, O. Muñiz, F. Perez-Jiménez, J. López-Miranda, J. Díaz, J. Vidal, et al. 2011. Clinical characteristics and evaluation of LDL-cholesterol treatment of the Spanish Familial Hypercholesterolemia Longitudinal Cohort Study (SAFEHEART). Lipids Health Dis. 10:94.
-
(2011)
Lipids Health Dis.
, vol.10
, pp. 94
-
-
Mata, N.1
Alonso, R.2
Badimón, L.3
Padró, T.4
Fuentes, F.5
Muñiz, O.6
Perez-Jiménez, F.7
López-Miranda, J.8
Díaz, J.9
Vidal, J.10
-
75
-
-
84896696778
-
Rationale and design of the familial hypercholesterolemia foundation cascade screening for awareness and detection of familial hypercholesterolemia registry
-
e17
-
O'Brien, E., M. Roe, E. Fraulo, E. Peterson, C. Ballantyne, J. Genest, S. Gidding, E. Hammond, L. Hemphill, L. Hudgins, et al. 2014. Rationale and design of the familial hypercholesterolemia foundation cascade screening for awareness and detection of familial hypercholesterolemia registry. Am. Heart J. 167:342-349. e17.
-
(2014)
Am. Heart J.
, vol.167
, pp. 342-349
-
-
O'Brien, E.1
Roe, M.2
Fraulo, E.3
Peterson, E.4
Ballantyne, C.5
Genest, J.6
Gidding, S.7
Hammond, E.8
Hemphill, L.9
Hudgins, L.10
-
76
-
-
84941657356
-
Cascade screening in familial hypercholesterolemia: Advancing forward
-
Santos, R., T. Frauches, and A. Chacra. 2015. Cascade screening in familial hypercholesterolemia: advancing forward. J. Atheroscler. Thromb. 22:869-880.
-
(2015)
J. Atheroscler. Thromb.
, vol.22
, pp. 869-880
-
-
Santos, R.1
Frauches, T.2
Chacra, A.3
-
77
-
-
84963649271
-
A systematic review of current studies in patients with familial hypercholesterolemia by use of national familial hypercholesterolemia registries
-
Mundal, L., and K. Retterstl. 2016. A systematic review of current studies in patients with familial hypercholesterolemia by use of national familial hypercholesterolemia registries. Curr. Opin. Lipidol. 27:388-397.
-
(2016)
Curr. Opin. Lipidol.
, vol.27
, pp. 388-397
-
-
Mundal, L.1
Retterstl, K.2
-
78
-
-
0032890205
-
Mortality in treated heterozygous familial hypercholesterolaemia: Implications for clinical management. Scientific Steering Committee on behalf of the Simon Broome Register Group
-
1999. Mortality in treated heterozygous familial hypercholesterolaemia: implications for clinical management. Scientific Steering Committee on behalf of the Simon Broome Register Group. Atherosclerosis. 142:105-112.
-
(1999)
Atherosclerosis.
, vol.142
, pp. 105-112
-
-
-
79
-
-
84966642427
-
Patients with familial hypercholesterolaemia are characterized by presence of cardiovascular disease at the time of death
-
Krogh, H., L. Mundal, K. Holven, and K. Retterstøl. 2016. Patients with familial hypercholesterolaemia are characterized by presence of cardiovascular disease at the time of death. Eur. Heart J. 37:1398-1405.
-
(2016)
Eur. Heart J.
, vol.37
, pp. 1398-1405
-
-
Krogh, H.1
Mundal, L.2
Holven, K.3
Retterstøl, K.4
-
80
-
-
52049109169
-
Cardiovascular disease in familial hypercholesterolaemia: Influence of low-density lipoprotein receptor mutation type and classic risk factors
-
Alonso, R., N. Mata, S. Castillo, F. Fuentes, P. Saenz, O. Muñiz, J. Galiana, R. Figueras, J. Diaz, P. Gomez-Enterría, et al. 2008. Cardiovascular disease in familial hypercholesterolaemia: influence of low-density lipoprotein receptor mutation type and classic risk factors. Atherosclerosis. 200:315-321.
-
(2008)
Atherosclerosis.
, vol.200
, pp. 315-321
-
-
Alonso, R.1
Mata, N.2
Castillo, S.3
Fuentes, F.4
Saenz, P.5
Muñiz, O.6
Galiana, J.7
Figueras, R.8
Diaz, J.9
Gomez-Enterría, P.10
-
81
-
-
82955189685
-
Maternal inheritance of familial hypercholesterolemia caused by the V408M low-density lipoprotein receptor mutation increases mortality
-
Versmissen, J., I. Botden, R. Huijgen, D. Oosterveer, J. Defesche, T. Heil, A. Muntz, J. Langendonk, A. Schinkel, J. Kastelein, et al. 2011. Maternal inheritance of familial hypercholesterolemia caused by the V408M low-density lipoprotein receptor mutation increases mortality. Atherosclerosis. 219:690-693.
-
(2011)
Atherosclerosis.
, vol.219
, pp. 690-693
-
-
Versmissen, J.1
Botden, I.2
Huijgen, R.3
Oosterveer, D.4
Defesche, J.5
Heil, T.6
Muntz, A.7
Langendonk, J.8
Schinkel, A.9
Kastelein, J.10
-
82
-
-
84942509791
-
Familial hypercholesterolaemia: A global call to arms
-
Vallejo-Vaz, A., S. Kondapally Seshasai, D. Cole, G. Hovingh, J. Kastelein, P. Mata, F. Raal, R. Santos, H. Soran, G. Watts, et al. 2015. Familial hypercholesterolaemia: a global call to arms. Atherosclerosis. 243:257-259.
-
(2015)
Atherosclerosis.
, vol.243
, pp. 257-259
-
-
Vallejo-Vaz, A.1
Kondapally Seshasai, S.2
Cole, D.3
Hovingh, G.4
Kastelein, J.5
Mata, P.6
Raal, F.7
Santos, R.8
Soran, H.9
Watts, G.10
-
83
-
-
84857619617
-
Cascade screening for familial hypercholesterolemia (FH)
-
Ned, R., and E. Sijbrands. 2011. Cascade screening for familial hypercholesterolemia (FH). PLoS Curr. 3: RRN1238.
-
(2011)
PLoS Curr.
, vol.3
, pp. RRN1238
-
-
Ned, R.1
Sijbrands, E.2
-
84
-
-
44849083647
-
-
National Collaborating Centre for Primary Care and Royal College of General Practitioners, London
-
DeMott, K., L. Nherera, EJ. Shaw, R. Minhas, SE. Humphries, M. Kathoria, G. Ritchie, V. Nunes, D. Davies, P. Lee, et al. 2008. Clinical Guidelines and Evidence Review for Familial Hypercholesterolaemia: the identification and management of adults and children with familial hypercholesterolaemia.. National Collaborating Centre for Primary Care and Royal College of General Practitioners, London.
-
(2008)
Clinical Guidelines and Evidence Review for Familial Hypercholesterolaemia: The Identification and Management of Adults and Children with Familial hypercholesterolaemia..
-
-
DeMott, K.1
Nherera, L.2
Shaw, E.J.3
Minhas, R.4
Humphries, S.E.5
Kathoria, M.6
Ritchie, G.7
Nunes, V.8
Davies, D.9
Lee, P.10
-
85
-
-
84978736631
-
Diagnostic scoring for familial hypercholesterolaemia in practice
-
Haralambos, K., P. Ashfield-Watt, and I. McDowell. 2016. Diagnostic scoring for familial hypercholesterolaemia in practice. Curr. Opin. Lipidol. 27:367-374.
-
(2016)
Curr. Opin. Lipidol.
, vol.27
, pp. 367-374
-
-
Haralambos, K.1
Ashfield-Watt, P.2
McDowell, I.3
-
86
-
-
0025944056
-
Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group
-
1991. Risk of fatal coronary heart disease in familial hypercholesterolaemia. Scientific Steering Committee on behalf of the Simon Broome Register Group. BMJ. 303:893-896.
-
(1991)
BMJ.
, vol.303
, pp. 893-896
-
-
-
87
-
-
0027301629
-
Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics
-
Williams, R., S. Hunt, M. Schumacher, R. Hegele, M. Leppert, E. Ludwig, and P. Hopkins. 1993. Diagnosing heterozygous familial hypercholesterolemia using new practical criteria validated by molecular genetics. Am. J. Cardiol. 72:171-176.
-
(1993)
Am. J. Cardiol.
, vol.72
, pp. 171-176
-
-
Williams, R.1
Hunt, S.2
Schumacher, M.3
Hegele, R.4
Leppert, M.5
Ludwig, E.6
Hopkins, P.7
-
88
-
-
0002798531
-
-
WHO Human Genetics Programme, Geneva, 4 September, World Health Organization, Geneva. Accessed September 20, 2016
-
WHO Human Genetics Programme. 1999. Familial hypercholesterolaemia (FH): report of a second WHO consultation, Geneva, 4 September 1998. World Health Organization, Geneva. Accessed September 20, 2016, at http://www.who.int/iris/handle/10665/66346.
-
(1998)
Familial Hypercholesterolaemia (FH): Report of a Second WHO Consultation
-
-
-
89
-
-
84924965687
-
Clinical experience of scoring criteria for familial hypercholesterolaemia (FH) genetic testing in Wales
-
Haralambos, K., S. D. Whatley, R. Edwards, R. Gingell, D. Townsend, P. Ashfield-Watt, P. Lansberg, D. B. Datta, and I. F. McDowell. 2015. Clinical experience of scoring criteria for familial hypercholesterolaemia (FH) genetic testing in Wales. Atherosclerosis. 240:190-196.
-
(2015)
Atherosclerosis.
, vol.240
, pp. 190-196
-
-
Haralambos, K.1
Whatley, S.D.2
Edwards, R.3
Gingell, R.4
Townsend, D.5
Ashfield-Watt, P.6
Lansberg, P.7
Datta, D.B.8
McDowell, I.F.9
-
90
-
-
0035915685
-
Review of first 5 years of screening for familial hypercholesterolemia in the Netherlands
-
Umans-Eckenhausen, M. A., J. C. Defesche, E. J. Sijbrands, R. L. Scheerder, and J. J. Kastelein. 2001. Review of first 5 years of screening for familial hypercholesterolemia in the Netherlands. Lancet. 357:165-168.
-
(2001)
Lancet.
, vol.357
, pp. 165-168
-
-
Umans-Eckenhausen, M.A.1
Defesche, J.C.2
Sijbrands, E.J.3
Scheerder, R.L.4
Kastelein, J.J.5
-
91
-
-
77957880779
-
Defining the challenges of FH screening for familial hypercholesterolemia
-
Defesche, J. 2010. Defining the challenges of FH screening for familial hypercholesterolemia. J. Clin. Lipidol. 4:338-341.
-
(2010)
J. Clin. Lipidol.
, vol.4
, pp. 338-341
-
-
Defesche, J.1
-
92
-
-
84920160399
-
Improving identification of familial hypercholesterolaemia in primary care: Derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT)
-
Weng, S., J. Kai, H. Andrew Neil, S. Humphries, and N. Qureshi. 2015. Improving identification of familial hypercholesterolaemia in primary care: derivation and validation of the familial hypercholesterolaemia case ascertainment tool (FAMCAT). Atherosclerosis. 238:336-343.
-
(2015)
Atherosclerosis.
, vol.238
, pp. 336-343
-
-
Weng, S.1
Kai, J.2
Andrew Neil, H.3
Humphries, S.4
Qureshi, N.5
-
93
-
-
84966373141
-
Cardiovascular risk stratification in familial hypercholesterolaemia
-
Sharifi, M., R. Rakhit, S. Humphries, and D. Nair. 2016. Cardiovascular risk stratification in familial hypercholesterolaemia. Heart. 102:1003-1008.
-
(2016)
Heart.
, vol.102
, pp. 1003-1008
-
-
Sharifi, M.1
Rakhit, R.2
Humphries, S.3
Nair, D.4
-
94
-
-
84908397421
-
National Lipid Association recommendations for patient-centered management of dyslipidemia: Part 1-executive summary
-
Jacobson, T. A., M. K. Ito, K. C. Maki, C. E. Orringer, H. E. Bays, P. H. Jones, J. M. McKenney, S. M. Grundy, E. A. Gill, R. A. Wild, et al. 2014. National Lipid Association recommendations for patient-centered management of dyslipidemia: part 1-executive summary. J. Clin. Lipidol. 8:473-488.
-
(2014)
J. Clin. Lipidol.
, vol.8
, pp. 473-488
-
-
Jacobson, T.A.1
Ito, M.K.2
Maki, K.C.3
Orringer, C.E.4
Bays, H.E.5
Jones, P.H.6
McKenney, J.M.7
Grundy, S.M.8
Gill, E.A.9
Wild, R.A.10
-
95
-
-
84988672681
-
2016 European Guidelines on cardiovascular disease prevention in clinical practice
-
The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR)
-
M. F. Piepoli, A. W. Hoes, S. Agewall, C. Albus, C. Brotons, A. L. Catapano, M. T. Cooney, U. Corrà, B. Cosyns, C. Deaton, et al. 2016. 2016 European Guidelines on cardiovascular disease prevention in clinical practice: The Sixth Joint Task Force of the European Society of Cardiology and Other Societies on Cardiovascular Disease Prevention in Clinical Practice (constituted by representatives of 10 societies and by invited experts) Developed with the special contribution of the European Association for Cardiovascular Prevention & Rehabilitation (EACPR). Atherosclerosis. 252:207-274.
-
(2016)
Atherosclerosis.
, vol.252
, pp. 207-274
-
-
Piepoli, M.F.1
Hoes, A.W.2
Agewall, S.3
Albus, C.4
Brotons, C.5
Catapano, A.L.6
Cooney, M.T.7
Corrà, U.8
Cosyns, B.9
Deaton, C.10
-
96
-
-
84893647246
-
Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation
-
Watts, G., S. Gidding, A. Wierzbicki, P. Toth, R. Alonso, W. Brown, E. Bruckert, J. Defesche, K. Lin, M. Livingston, et al. 2014. Integrated guidance on the care of familial hypercholesterolaemia from the International FH Foundation. Int. J. Cardiol. 171:309-325.
-
(2014)
Int. J. Cardiol.
, vol.171
, pp. 309-325
-
-
Watts, G.1
Gidding, S.2
Wierzbicki, A.3
Toth, P.4
Alonso, R.5
Brown, W.6
Bruckert, E.7
Defesche, J.8
Lin, K.9
Livingston, M.10
-
97
-
-
84872376838
-
Statin treatment of children with familial hypercholesterolemia-trying to balance incomplete evidence of longterm safety and clinical accountability: Are we approaching a consensus?
-
Vuorio, A., K. Docherty, S. Humphries, J. Kuoppala, and P. Kovanen. 2013. Statin treatment of children with familial hypercholesterolemia-trying to balance incomplete evidence of longterm safety and clinical accountability: Are we approaching a consensus? Atherosclerosis. 226:315-320.
-
(2013)
Atherosclerosis.
, vol.226
, pp. 315-320
-
-
Vuorio, A.1
Docherty, K.2
Humphries, S.3
Kuoppala, J.4
Kovanen, P.5
-
98
-
-
55749088063
-
Reductions in allcause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: A prospective registry study
-
Neil, A., J. Cooper, J. Betteridge, N. Capps, I. McDowell, P. Durrington, M. Seed, and S. Humphries. 2008. Reductions in allcause, cancer, and coronary mortality in statin-treated patients with heterozygous familial hypercholesterolaemia: a prospective registry study. Eur. Heart J. 29:2625-2633.
-
(2008)
Eur. Heart J.
, vol.29
, pp. 2625-2633
-
-
Neil, A.1
Cooper, J.2
Betteridge, J.3
Capps, N.4
McDowell, I.5
Durrington, P.6
Seed, M.7
Humphries, S.8
-
99
-
-
77955779223
-
Impact of statin treatment on the clinical fate of heterozygous familial hypercholesterolemia
-
Harada-Shiba, M., T. Sugisawa, H. Makino, M. Abe, M. Tsushima, Y. Yoshimasa, T. Yamashita, Y. Miyamoto, A. Yamamoto, H. Tomoike, et al. 2010. Impact of statin treatment on the clinical fate of heterozygous familial hypercholesterolemia. J. Atheroscler. Thromb. 17:667-674.
-
(2010)
J. Atheroscler. Thromb.
, vol.17
, pp. 667-674
-
-
Harada-Shiba, M.1
Sugisawa, T.2
Makino, H.3
Abe, M.4
Tsushima, M.5
Yoshimasa, Y.6
Yamashita, T.7
Miyamoto, Y.8
Yamamoto, A.9
Tomoike, H.10
-
100
-
-
84973523741
-
Cardiovascular disease risk associated with familial hypercholesterolemia: A systematic review of the literature
-
Wong, B., G. Kruse, L. Kutikova, K. Ray, P. Mata, and E. Bruckert. 2016. Cardiovascular disease risk associated with familial hypercholesterolemia: a systematic review of the literature. Clin. Ther. 38:1696-1709.
-
(2016)
Clin. Ther.
, vol.38
, pp. 1696-1709
-
-
Wong, B.1
Kruse, G.2
Kutikova, L.3
Ray, K.4
Mata, P.5
Bruckert, E.6
-
102
-
-
84964378012
-
Identifying familial hypercholesterolemia in acute coronary syndrome
-
Gencera, B., and D. Nanchen. 2016. Identifying familial hypercholesterolemia in acute coronary syndrome. Curr. Opin. Lipidol. 27:375-381.
-
(2016)
Curr. Opin. Lipidol.
, vol.27
, pp. 375-381
-
-
Gencera, B.1
Nanchen, D.2
-
103
-
-
77049105368
-
Evaluation of cholesterol lowering treatment of patients with familial hypercholesterolemia: A large cross-sectional study in The Netherlands
-
Pijlman, A. H., R. Huijgen, S. N. Verhagen, B. P. Imholz, A. H. Liam, J. J. Kastelein, E. J. Abbink, A. F. Stalenhoef, and F. L. Visseren. 2010. Evaluation of cholesterol lowering treatment of patients with familial hypercholesterolemia: a large cross-sectional study in The Netherlands. Atherosclerosis. 209:189-194.
-
(2010)
Atherosclerosis.
, vol.209
, pp. 189-194
-
-
Pijlman, A.H.1
Huijgen, R.2
Verhagen, S.N.3
Imholz, B.P.4
Liam, A.H.5
Kastelein, J.J.6
Abbink, E.J.7
Stalenhoef, A.F.8
Visseren, F.L.9
-
104
-
-
84975728140
-
Treatment gaps in adults with heterozygous familial hypercholesterolemia in the United States
-
deGoma, E., Z. Ahmad, E. O'Brien, I. Kindt, P. Shrader, C. Newman, Y. Pokharel, S. Baum, L. Hemphill, L. Hudgins, et al. 2016. Treatment gaps in adults with heterozygous familial hypercholesterolemia in the United States. Circ Cardiovasc Genet. 9:240-249.
-
(2016)
Circ Cardiovasc Genet.
, vol.9
, pp. 240-249
-
-
DeGoma, E.1
Ahmad, Z.2
O'Brien, E.3
Kindt, I.4
Shrader, P.5
Newman, C.6
Pokharel, Y.7
Baum, S.8
Hemphill, L.9
Hudgins, L.10
-
105
-
-
44149123549
-
Recommendations for the use of LDL apheresis
-
Thompson, G. 2008. Recommendations for the use of LDL apheresis. Atherosclerosis. 198:247-255.
-
(2008)
Atherosclerosis.
, vol.198
, pp. 247-255
-
-
Thompson, G.1
-
106
-
-
84949321606
-
The agenda for familial hypercholesterolemia
-
Gidding, S., M. Ann Champagne, S. de Ferranti, J. Defesche, M. Ito, J. Knowles, B. McCrindle, F. Raal, D. Rader, R. Santos, et al. 2015. The agenda for familial hypercholesterolemia. Circulation. 132:2167-2192.
-
(2015)
Circulation.
, vol.132
, pp. 2167-2192
-
-
Gidding, S.1
Ann Champagne, M.2
De Ferranti, S.3
Defesche, J.4
Ito, M.5
Knowles, J.6
McCrindle, B.7
Raal, F.8
Rader, D.9
Santos, R.10
-
107
-
-
84969962145
-
Defining severe familial hypercholesterolaemia and the implications for clinical management: A consensus statement from the International Atherosclerosis Society Severe Familial Hypercholesterolemia Panel
-
Santos, R., S. Gidding, R. Hegele, M. Cuchel, P. Barter, G. Watts, S. Baum, A. Catapano, M. Chapman, J. Defesche, et al. 2016. Defining severe familial hypercholesterolaemia and the implications for clinical management: a consensus statement from the International Atherosclerosis Society Severe Familial Hypercholesterolemia Panel. Lancet Diabetes Endocrinol. 4:850-861.
-
(2016)
Lancet Diabetes Endocrinol.
, vol.4
, pp. 850-861
-
-
Santos, R.1
Gidding, S.2
Hegele, R.3
Cuchel, M.4
Barter, P.5
Watts, G.6
Baum, S.7
Catapano, A.8
Chapman, M.9
Defesche, J.10
-
108
-
-
77953370879
-
Encuesta sobre el manejo de dislipidemia con estatinas en México: Porcentaje de pacientes que alcanzan las metas establecidas por el Programa Nacional de Educación en Colesterol (National Cholesterol Education Program [NCEP])
-
González, C. A., A. Pavía, F. J. Redding, J. L. Zacarías, M. A. Ramírez, M. Alpízar, J. Aspe, J. Carranza, R. Barba, J. C. Ramírez, et al. 2009. Encuesta sobre el manejo de dislipidemia con estatinas en México: Porcentaje de pacientes que alcanzan las metas establecidas por el Programa Nacional de Educación en Colesterol (National Cholesterol Education Program [NCEP]). Rev Mex Cardiol. 20:18-22.
-
(2009)
Rev Mex Cardiol.
, vol.20
, pp. 18-22
-
-
González, C.A.1
Pavía, A.2
Redding, F.J.3
Zacarías, J.L.4
Ramírez, M.A.5
Alpízar, M.6
Aspe, J.7
Carranza, J.8
Barba, R.9
Ramírez, J.C.10
-
109
-
-
84943166318
-
Availability and affordability of new medicines in Latin American countries where pivotal clinical trials were conducted
-
Homedes, N., and A. Ugalde. 2015. Availability and affordability of new medicines in Latin American countries where pivotal clinical trials were conducted. Bull. World Health Organ. 93:674-683.
-
(2015)
Bull. World Health Organ.
, vol.93
, pp. 674-683
-
-
Homedes, N.1
Ugalde, A.2
-
110
-
-
11144312891
-
-
WHO Environmental Burden of Disease Series, No. 1. World Health Organization, Geneva, Switzerland
-
Prüss-Üstün A., C. Mathers, C. Corvalán, and A. Woodward. 2003. Introduction and methods: assessing the environmental burden of disease at national and local levels.. WHO Environmental Burden of Disease Series, No. 1. World Health Organization, Geneva, Switzerland.
-
(2003)
Introduction and Methods: Assessing the Environmental Burden of Disease at National and Local levels..
-
-
Prüss-Üstün, A.1
Mathers, C.2
Corvalán, C.3
Woodward, A.4
-
111
-
-
79959347897
-
Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies
-
Nherera, L., D. Marks, R. Minhas, M. Thorogood, and S. Humphries. 2011. Probabilistic cost-effectiveness analysis of cascade screening for familial hypercholesterolaemia using alternative diagnostic and identification strategies. Heart. 97:1175-1181.
-
(2011)
Heart.
, vol.97
, pp. 1175-1181
-
-
Nherera, L.1
Marks, D.2
Minhas, R.3
Thorogood, M.4
Humphries, S.5
-
112
-
-
84908129423
-
Daily life, experience and needs of persons suffering from homozygous familial hypercholesterolaemia: Insights from a patient survey
-
Bruckert, E., S. Saheb, J. Bonté, and C. Coudray-Omnès. 2014. Daily life, experience and needs of persons suffering from homozygous familial hypercholesterolaemia: Insights from a patient survey. Atheroscler. Suppl. 15:46-51.
-
(2014)
Atheroscler. Suppl.
, vol.15
, pp. 46-51
-
-
Bruckert, E.1
Saheb, S.2
Bonté, J.3
Coudray-Omnès, C.4
-
113
-
-
84897456270
-
Quality of life in a cohort of familial hypercholesterolemia patients from the south of Europe
-
Mata, N., R. Alonso, J. Banegas, D. Zambon, A. Brea, and P. Mata. 2014. Quality of life in a cohort of familial hypercholesterolemia patients from the south of Europe. Eur. J. Public Health. 24:221-225.
-
(2014)
Eur. J. Public Health.
, vol.24
, pp. 221-225
-
-
Mata, N.1
Alonso, R.2
Banegas, J.3
Zambon, D.4
Brea, A.5
Mata, P.6
-
114
-
-
19444387758
-
Familial hypercholesterolemia: Ethical, practical and psychological problems from the perspective of patients
-
Ågård, A., I. Bolmsjö, G. Hermerén, and J. Wahlstöm. 2005. Familial hypercholesterolemia: ethical, practical and psychological problems from the perspective of patients. Patient Educ. Couns. 57:162-167.
-
(2005)
Patient Educ. Couns.
, vol.57
, pp. 162-167
-
-
Ågård, A.1
Bolmsjö, I.2
Hermerén, G.3
Wahlstöm, J.4
-
115
-
-
84964808487
-
Familial hypercholesterolaemia reduces the quality of life of patients not reaching treatment targets
-
Mortensen, G. L., I. B. Madsen, C. Kruse, and H. Bundgaard. 2016. Familial hypercholesterolaemia reduces the quality of life of patients not reaching treatment targets. Dan. Med. J. 63:A5224.
-
(2016)
Dan. Med. J.
, vol.63
, pp. A5224
-
-
Mortensen, G.L.1
Madsen, I.B.2
Kruse, C.3
Bundgaard, H.4
-
116
-
-
84975217721
-
Hipercolesterolemia familiar: Artículo de revisión
-
Merchán, A., A. J. Ruiz, R. Campo, C. E. Prada, J. M. Toro, R. Sánchez, J. E. Gómez, N. I. Jaramillo, D. I. Molina, H. Vargas-Uricoechea, et al. 2016. Hipercolesterolemia familiar: artículo de revisión. Rev. Colomb. Cardiol. 23(S4):4-26.
-
(2016)
Rev. Colomb. Cardiol.
, vol.23
, Issue.S4
, pp. 4-26
-
-
Merchán, A.1
Ruiz, A.J.2
Campo, R.3
Prada, C.E.4
Toro, J.M.5
Sánchez, R.6
Gómez, J.E.7
Jaramillo, N.I.8
Molina, D.I.9
Vargas-Uricoechea, H.10
-
117
-
-
84855501197
-
Familial hypercholesterolaemia: A model of care for Australasia
-
Watts, G., D. Sullivan, N. Poplawski, F. van Bockxmeer, I. Hamilton-Craig, P. Clifton, R. O'Brien, W. Bishop, P. George, P. Barter, et al. 2011. Familial hypercholesterolaemia: A model of care for Australasia. Atheroscler. Suppl. 12:221-263.
-
(2011)
Atheroscler. Suppl.
, vol.12
, pp. 221-263
-
-
Watts, G.1
Sullivan, D.2
Poplawski, N.3
Van Bockxmeer, F.4
Hamilton-Craig, I.5
Clifton, P.6
O'Brien, R.7
Bishop, W.8
George, P.9
Barter, P.10
|