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Artigo de periodico
Sailing the Uncharted Waters of Familial Hypercholesterolemia LDL Receptor Genetic-Related Variants Land in Sight? (2023)
Santos Filho, Raul Dias dos
Source: Jacc-basic to translational science. Unidade: FM
Subjects: COLESTEROL, HIPERCOLESTEROLEMIA, DOENÇAS HEREDITÁRIAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS FILHO, Raul Dias dos. Sailing the Uncharted Waters of Familial Hypercholesterolemia LDL Receptor Genetic-Related Variants Land in Sight?. Jacc-basic to translational science, v. 8, n. 8, p. 1022-1024, 2023Tradução . . Disponível em: https://observatorio.fm.usp.br/handle/OPI/56005. Acesso em: 19 nov. 2024.
APA
Santos Filho, R. D. dos. (2023). Sailing the Uncharted Waters of Familial Hypercholesterolemia LDL Receptor Genetic-Related Variants Land in Sight? Jacc-basic to translational science, 8( 8), 1022-1024. doi:10.1016/j.jacbts.2023.05.014
NLM
Santos Filho RD dos. Sailing the Uncharted Waters of Familial Hypercholesterolemia LDL Receptor Genetic-Related Variants Land in Sight? [Internet]. Jacc-basic to translational science. 2023 ; 8( 8): 1022-1024.[citado 2024 nov. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56005
Vancouver
Santos Filho RD dos. Sailing the Uncharted Waters of Familial Hypercholesterolemia LDL Receptor Genetic-Related Variants Land in Sight? [Internet]. Jacc-basic to translational science. 2023 ; 8( 8): 1022-1024.[citado 2024 nov. 19 ] Available from: https://observatorio.fm.usp.br/handle/OPI/56005
Artigo de periodico
Homozygous familial hypercholesterolemia: phenotype rules! (2016)
Santos, Raul D.
Source: Atherosclerosis. Unidade: FM
Subjects: COLESTEROL, GENÓTIPOS, DOENÇAS HEREDITÁRIAS, HIPERCOLESTEROLEMIA, ARTERIOSCLEROSE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Raul D. Homozygous familial hypercholesterolemia: phenotype rules!. Atherosclerosis, v. 248, n. 1, p. 252-254, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.atherosclerosis.2016.03.009. Acesso em: 19 nov. 2024.
APA
Santos, R. D. (2016). Homozygous familial hypercholesterolemia: phenotype rules!. Atherosclerosis, 248( 1), 252-254. doi:10.1016/j.atherosclerosis.2016.03.009
NLM
Santos RD. Homozygous familial hypercholesterolemia: phenotype rules! [Internet]. Atherosclerosis. 2016 ; 248( 1): 252-254.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2016.03.009
Vancouver
Santos RD. Homozygous familial hypercholesterolemia: phenotype rules! [Internet]. Atherosclerosis. 2016 ; 248( 1): 252-254.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2016.03.009
Artigo de periodico
The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions (2012)
Carneiro, Marcia M.; Miname, Marcio H.; Gagliardi, Ana C.; Pereira, Carolina; Pereira, Alexandre C.; Krieger, José Eduardo; Maranhão, Raul Cavalcante ; Santos, Raul D.
Source: Atherosclerosis. Unidades: FM, FCF
Subjects: PLASMA, HIPERCOLESTEROLEMIA (GENÉTICA;METABOLISMO), DOENÇAS HEREDITÁRIAS, LIPOPROTEÍNAS LDL, EMULSÕES (FORMAS FARMACÊUTICAS)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARNEIRO, Marcia M. et al. The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions. Atherosclerosis, v. 221, n. 1, p. 268-274, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.atherosclerosis.2011.12.033. Acesso em: 19 nov. 2024.
APA
Carneiro, M. M., Miname, M. H., Gagliardi, A. C., Pereira, C., Pereira, A. C., Krieger, J. E., et al. (2012). The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions. Atherosclerosis, 221( 1), 268-274. doi:10.1016/j.atherosclerosis.2011.12.033
NLM
Carneiro MM, Miname MH, Gagliardi AC, Pereira C, Pereira AC, Krieger JE, Maranhão RC, Santos RD. The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions [Internet]. Atherosclerosis. 2012 ; 221( 1): 268-274.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2011.12.033
Vancouver
Carneiro MM, Miname MH, Gagliardi AC, Pereira C, Pereira AC, Krieger JE, Maranhão RC, Santos RD. The removal from plasma of chylomicrons and remnants is reduced in heterozygous familial hypercholesterolemia subjects with identified LDL receptor mutations: Study with artificial emulsions [Internet]. Atherosclerosis. 2012 ; 221( 1): 268-274.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2011.12.033
Artigo de periodico
Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment (2012)
Raal, Frederick J.; Santos, Raul D.
Source: Atherosclerosis. Unidade: FM
Subjects: DOENÇAS HEREDITÁRIAS, LIPOPROTEÍNAS, HIPERCOLESTEROLEMIA (DIAGNÓSTICO;TERAPIA), APOLIPOPROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RAAL, Frederick J. e SANTOS, Raul D. Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment. Atherosclerosis, v. 223, n. 2, p. 262-268, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.atherosclerosis.2012.02.019. Acesso em: 19 nov. 2024.
APA
Raal, F. J., & Santos, R. D. (2012). Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment. Atherosclerosis, 223( 2), 262-268. doi:10.1016/j.atherosclerosis.2012.02.019
NLM
Raal FJ, Santos RD. Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment [Internet]. Atherosclerosis. 2012 ; 223( 2): 262-268.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2012.02.019
Vancouver
Raal FJ, Santos RD. Homozygous familial hypercholesterolemia: Current perspectives on diagnosis and treatment [Internet]. Atherosclerosis. 2012 ; 223( 2): 262-268.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1016/j.atherosclerosis.2012.02.019
Artigo de periodico
Haemodynamic, metabolic and neuro-humoral abnormalities in young normotensive women at high familial risk for hypertension (2010)
Ciolac, E. G.; Bocchi, E. A.; Bortolotto, L. A.; Carvalho, V. O.; J M D Greve, J. M. D.; Guimarães, G. V.
Source: Journal of Human Hypertension. Unidade: FM
Subjects: HEMODINÂMICA, ENDOTÉLIO VASCULAR, DOENÇAS HEREDITÁRIAS, INSULINA, FATORES DE RISCO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CIOLAC, E. G. et al. Haemodynamic, metabolic and neuro-humoral abnormalities in young normotensive women at high familial risk for hypertension. Journal of Human Hypertension, v. 24, n. 12, p. 814-822, 2010Tradução . . Disponível em: https://doi.org/10.1038/jhh.2010.21. Acesso em: 19 nov. 2024.
APA
Ciolac, E. G., Bocchi, E. A., Bortolotto, L. A., Carvalho, V. O., J M D Greve, J. M. D., & Guimarães, G. V. (2010). Haemodynamic, metabolic and neuro-humoral abnormalities in young normotensive women at high familial risk for hypertension. Journal of Human Hypertension, 24( 12), 814-822. doi:10.1038/jhh.2010.21
NLM
Ciolac EG, Bocchi EA, Bortolotto LA, Carvalho VO, J M D Greve JMD, Guimarães GV. Haemodynamic, metabolic and neuro-humoral abnormalities in young normotensive women at high familial risk for hypertension [Internet]. Journal of Human Hypertension. 2010 ; 24( 12): 814-822.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/jhh.2010.21
Vancouver
Ciolac EG, Bocchi EA, Bortolotto LA, Carvalho VO, J M D Greve JMD, Guimarães GV. Haemodynamic, metabolic and neuro-humoral abnormalities in young normotensive women at high familial risk for hypertension [Internet]. Journal of Human Hypertension. 2010 ; 24( 12): 814-822.[citado 2024 nov. 19 ] Available from: https://doi.org/10.1038/jhh.2010.21

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