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Artigo de periodico
Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment (2015)
Wiegman, Albert; Gidding, Samuel S.; Watts, Gerald F.; Chapman, M. John; Ginsberg, Henry N.; Cuchel, Marina; Ose, Leiv; Averna, Maurizio; Boileau, Catherine; Borén, Jan; Bruckert, Eric; Catapano, Alberico L.; Defesche, Joep C.; Descamps, Olivier S.; Hegele, Robert A.; Hovingh, G. Kees; Humphries, Steve E.; Kovanen, Petri T.; Kuivenhoven, Jan Albert; Masana, Luis; Nordestgaard, Børge G.; Pajukanta, Päivi; Parhofer, Klaus G.; Raal, Frederick J.; Ray, Kausik K.; Santos, Raul D.; Stalenhoef, Anton F. H.; Steinhagen-Thiessen, Elisabeth; Stroes, Erik S.; Taskinen, Marja-Riitta; Tybjærg-Hansen, Anne; Wiklund, Olov
Fonte: European heart journal. Unidade: FM
Assuntos: ADOLESCENTES, CRIANÇAS, LIPÍDEOS (METABOLISMO), MUTAÇÃO GENÉTICA, HIPERCOLESTEROLEMIA (DIAGNÓSTICO;TERAPIA;TENDÊNCIAS)
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ABNT
WIEGMAN, Albert et al. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment. European heart journal, v. 36, p. 2425-2437, 2015Tradução . . Disponível em: https://doi.org/10.1093/eurheartj/ehv157. Acesso em: 11 nov. 2024.
APA
Wiegman, A., Gidding, S. S., Watts, G. F., Chapman, M. J., Ginsberg, H. N., Cuchel, M., et al. (2015). Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment. European heart journal, 36, 2425-2437. doi:10.1093/eurheartj/ehv157
NLM
Wiegman A, Gidding SS, Watts GF, Chapman MJ, Ginsberg HN, Cuchel M, Ose L, Averna M, Boileau C, Borén J, Bruckert E, Catapano AL, Defesche JC, Descamps OS, Hegele RA, Hovingh GK, Humphries SE, Kovanen PT, Kuivenhoven JA, Masana L, Nordestgaard BG, Pajukanta P, Parhofer KG, Raal FJ, Ray KK, Santos RD, Stalenhoef AFH, Steinhagen-Thiessen E, Stroes ES, Taskinen M-R, Tybjærg-Hansen A, Wiklund O. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment [Internet]. European heart journal. 2015 ; 36 2425-2437.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/eurheartj/ehv157
Vancouver
Wiegman A, Gidding SS, Watts GF, Chapman MJ, Ginsberg HN, Cuchel M, Ose L, Averna M, Boileau C, Borén J, Bruckert E, Catapano AL, Defesche JC, Descamps OS, Hegele RA, Hovingh GK, Humphries SE, Kovanen PT, Kuivenhoven JA, Masana L, Nordestgaard BG, Pajukanta P, Parhofer KG, Raal FJ, Ray KK, Santos RD, Stalenhoef AFH, Steinhagen-Thiessen E, Stroes ES, Taskinen M-R, Tybjærg-Hansen A, Wiklund O. Familial hypercholesterolaemia in children and adolescents: gaining decades of life by optimizing detection and treatment [Internet]. European heart journal. 2015 ; 36 2425-2437.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/eurheartj/ehv157
Artigo de periodico
Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society (2014)
Cuchel, Marina; Bruckert, Eric; Ginsberg, Henry N.; Raal, Frederick J.; Santos, Raul D.; Hegele, Robert A.; Kuivenhoven, Jan Albert; Nordestgaard, Børge G.; Descamps, Olivier S.; Steinhagen-Thiessen, Elisabeth; Tybjærg-Hansen, Anne; Watts, Gerald F.; Averna, Maurizio; Boileau, Catherine; Borén, Jan; Catapano, Alberico L.; Defesche, Joep C.; Hovingh, G. Kees; Humphries, Steve E.; Kovanen, Petri T.; Masana, Luis; Pajukanta, Päivi; Parhofer, Klaus G.; Ray, Kausik K.; Stalenhoef, Anton F. H.; Stroes, Erik; Taskinen, Marja-Riitta; Wiegman, Albert; Wiklund, Olov; Chapman, M. John
Fonte: European heart journal. Unidade: FM
Assuntos: GENÉTICA, LIPOPROTEÍNAS, ARTERIOSCLEROSE, HIPERCOLESTEROLEMIA (DIAGNÓSTICO)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CUCHEL, Marina et al. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. European heart journal, v. 35, n. 32, p. 2146-2157, 2014Tradução . . Disponível em: https://doi.org/10.1093/eurheartj/ehu274. Acesso em: 11 nov. 2024.
APA
Cuchel, M., Bruckert, E., Ginsberg, H. N., Raal, F. J., Santos, R. D., Hegele, R. A., et al. (2014). Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society. European heart journal, 35( 32), 2146-2157. doi:10.1093/eurheartj/ehu274
NLM
Cuchel M, Bruckert E, Ginsberg HN, Raal FJ, Santos RD, Hegele RA, Kuivenhoven JA, Nordestgaard BG, Descamps OS, Steinhagen-Thiessen E, Tybjærg-Hansen A, Watts GF, Averna M, Boileau C, Borén J, Catapano AL, Defesche JC, Hovingh GK, Humphries SE, Kovanen PT, Masana L, Pajukanta P, Parhofer KG, Ray KK, Stalenhoef AFH, Stroes E, Taskinen M-R, Wiegman A, Wiklund O, Chapman MJ. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society [Internet]. European heart journal. 2014 ; 35( 32): 2146-2157.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/eurheartj/ehu274
Vancouver
Cuchel M, Bruckert E, Ginsberg HN, Raal FJ, Santos RD, Hegele RA, Kuivenhoven JA, Nordestgaard BG, Descamps OS, Steinhagen-Thiessen E, Tybjærg-Hansen A, Watts GF, Averna M, Boileau C, Borén J, Catapano AL, Defesche JC, Hovingh GK, Humphries SE, Kovanen PT, Masana L, Pajukanta P, Parhofer KG, Ray KK, Stalenhoef AFH, Stroes E, Taskinen M-R, Wiegman A, Wiklund O, Chapman MJ. Homozygous familial hypercholesterolaemia: new insights and guidance for clinicians to improve detection and clinical management. A position paper from the Consensus Panel on Familial Hypercholesterolaemia of the European Atherosclerosis Society [Internet]. European heart journal. 2014 ; 35( 32): 2146-2157.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1093/eurheartj/ehu274
Artigo de periodico
Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency (2008)
Santos, Raul D.; Schaefer, Ernst J.; Asztalos, Bela F.; Polisecki, Eliana; Wang, Jian; Hegele, Robert A.; Martinez, Lilton R. C.; Miname, Marcio H.; Rochitte, Carlos E.; Luz, Protasio Da; Maranhão, Raul Cavalcante
Fonte: Journal of Lipid Research. Unidades: FM, FCF
Assuntos: LIPOPROTEÍNAS (GENÉTICA), APOLIPROTEÍNAS (GENÉTICA), CORONARIOPATIA (PATOLOGIA), CARDIOPATIAS (PATOLOGIA), ARTERIOSCLEROSE CORONÁRIA (ETIOLOGIA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Raul D. et al. Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency. Journal of Lipid Research, v. 49, n. 2, p. 349-357, 2008Tradução . . Disponível em: https://doi.org/10.1194/jlr.M700362-JLR200. Acesso em: 11 nov. 2024.
APA
Santos, R. D., Schaefer, E. J., Asztalos, B. F., Polisecki, E., Wang, J., Hegele, R. A., et al. (2008). Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency. Journal of Lipid Research, 49( 2), 349-357. doi:10.1194/jlr.M700362-JLR200
NLM
Santos RD, Schaefer EJ, Asztalos BF, Polisecki E, Wang J, Hegele RA, Martinez LRC, Miname MH, Rochitte CE, Luz PD, Maranhão RC. Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency [Internet]. Journal of Lipid Research. 2008 ; 49( 2): 349-357.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1194/jlr.M700362-JLR200
Vancouver
Santos RD, Schaefer EJ, Asztalos BF, Polisecki E, Wang J, Hegele RA, Martinez LRC, Miname MH, Rochitte CE, Luz PD, Maranhão RC. Characterization of high density lipoprotein particles in familial apolipoprotein A-I deficiency [Internet]. Journal of Lipid Research. 2008 ; 49( 2): 349-357.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1194/jlr.M700362-JLR200
Artigo de periodico
Cockayne syndrome type A: novel mutations in eight typical patients (2006)
Bertola, Debora R.; Cao, Henian; Albano, Lilian M. J.; Kok, Fernando; Marques-Dias, Maria Joaquina; Kim, Chong A.; Hegele, Robert A.
Fonte: Journal of human genetics. Unidade: FM
Assuntos: MUTAÇÃO GENÉTICA, GENÓTIPOS, FENÓTIPOS, DOENÇAS NEURODEGENERATIVAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERTOLA, Debora R. et al. Cockayne syndrome type A: novel mutations in eight typical patients. Journal of human genetics, v. 51, n. 8, p. 701-705, 2006Tradução . . Disponível em: https://doi.org/10.1007/s10038-006-0011-7. Acesso em: 11 nov. 2024.
APA
Bertola, D. R., Cao, H., Albano, L. M. J., Kok, F., Marques-Dias, M. J., Kim, C. A., & Hegele, R. A. (2006). Cockayne syndrome type A: novel mutations in eight typical patients. Journal of human genetics, 51( 8), 701-705. doi:10.1007/s10038-006-0011-7
NLM
Bertola DR, Cao H, Albano LMJ, Kok F, Marques-Dias MJ, Kim CA, Hegele RA. Cockayne syndrome type A: novel mutations in eight typical patients [Internet]. Journal of human genetics. 2006 ;51( 8): 701-705.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10038-006-0011-7
Vancouver
Bertola DR, Cao H, Albano LMJ, Kok F, Marques-Dias MJ, Kim CA, Hegele RA. Cockayne syndrome type A: novel mutations in eight typical patients [Internet]. Journal of human genetics. 2006 ;51( 8): 701-705.[citado 2024 nov. 11 ] Available from: https://doi.org/10.1007/s10038-006-0011-7

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