Zobrazeno 1 - 10
of 637
pro vyhledávání: '"Santos RD"'
Autor:
Watts, GF, Gidding, SS, Hegele, RA, Raal, FJ, Sturm, AC, Jones, LK, Sarkies, MN, Al-Rasadi, K, Blom, DJ, Daccord, M, De Ferranti, SD, Folco, E, Libby, P, Mata, P, Nawawi, HM, Ramaswami, U, Ray, KK, Stefanutti, C, Yamashita, S, Pang, J, Thompson, GR, Santos, RD
This contemporary, international, evidence-informed guidance aims to achieve the greatest good for the greatest number of people with familial hypercholesterolaemia (FH) across different countries. FH, a family of monogenic defects in the hepatic LDL
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::178f2780d50a40cd0f8c2395f65be6ce
http://hdl.handle.net/10044/1/105073
http://hdl.handle.net/10044/1/105073
Publikováno v:
Liver International. 42:1772-1782
Background and aims:Even as several pharmacological treatments for non-alcoholic steatohepatitis (NASH) are in development, the incidence of NASH is increasing on an international scale. We aim to assess clinical practice gaps and challenges of hepat
Autor:
Zorzo RA, Suen VMM, Santos JE, null Silva-Jr, Suazo VK, Honorato ALSC, Santos RD, Jannes CE, A Pereira, Krieger JE, null Liberatore-Jr
Familial hypercholesterolemia (FH) is characterized by high low-density lipoprotein cholesterol (LDL-C) levels and a high risk of early coronary heart disease. Structural alterations in the LDLR, APOB, and PCSK9 genes were not found in 20–40% of pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::146e71a053e9c9f8bf00c6640f09e1ac
https://doi.org/10.21203/rs.3.rs-2268996/v1
https://doi.org/10.21203/rs.3.rs-2268996/v1
Autor:
Flávia Moraes Silva, Júlia Lima Rd, Victoria Silva Chites Rd, Carolina Oliveira dos Santos Rd, Camila Ferri Burgel
Publikováno v:
Journal of Parenteral and Enteral Nutrition. 46:887-895
BACKGROUND "Gold standard" methods for muscle mass (MM) assessment are expensive and difficult to use in clinical practice. The present study aimed to evaluate the association between easy-to-apply and low-cost indicators of MM and clinical outcomes
Autor:
Nepomuceno, LS, Bessa, AKM, Araújo, LMDSR, Santos, RD, Oliveira, JSR, Calegare, SR, Alves, ST
Publikováno v:
In Hematology, Transfusion and Cell Therapy October 2023 45 Supplement 4:S607-S607
Autor:
dos Santos RD, Carolina Oliveira, Burgel, Camila Ferri, Chites RD, Victoria Silva, Lima RD, Júlia, Silva PhD, Flávia Moraes
Publikováno v:
JPEN Journal of Parenteral & Enteral Nutrition; May2022, Vol. 46 Issue 4, p887-895, 9p
Autor:
Wilemon, KA, Patel, J, Aguilar-Salinas, C, Ahmed, CD, Alkhnifsawi, M, Almahmeed, W, Alonso, R, Al-Rasadi, K, Badimon, L, Bernal, LM, Bogsrud, MP, Braun, LT, Brunham, L, Catapano, AL, Cillikova, K, Corral, P, Cuevas, R, Defesche, JC, Descamps, OS, de Ferranti, S, Eisele, JL, Elikir, G, Folco, E, Freiberger, T, Fuggetta, F, Gaspar, IM, Gesztes, AG, Groselj, U, Hamilton-Craig, I, Hanauer-Mader, G, Harada-Shiba, M, Hastings, G, Hovingh, GK, Izar, MC, Jamison, A, Karlsson, GN, Kayikcioglu, M, Koob, S, Koseki, M, Lane, S, Lima-Martinez, MM, Lopez, G, Martinez, TL, Marais, D, Marion, L, Mata, P, Maurina, I, Maxwell, D, Mehta, R, Mensah, GA, Miserez, AR, Neely, D, Nicholls, SJ, Nohara, A, Nordestgaard, BG, Ose, L, Pallidis, A, Pang, J, Payne, J, Peterson, AL, Popescu, MP, Puri, R, Ray, KK, Reda, A, Sampietro, T, Santos, RD, Schalkers, I, Schreier, L, Shapiro, MD, Sijbrands, E, Soffer, D, Stefanutti, C, Stoll, M, Sy, RG, Tamayo, ML, Tilney, MK, Tokgozoglu, L, Tomlinson, B, Vallejo-Vaz, AJ, Vazquez-Cardenas, A, de Luca, PV, Wald, DS, Watts, GF, Wenger, NK, Wolf, M, Wood, D, Zegerius, A, Gaziano, TA, Gidding, SS, Global Familial
Publikováno v:
JAMA Cardiology
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
ImportanceFamilial hypercholesterolemia (FH) is an underdiagnosed and undertreated genetic disorder that leads to premature morbidity and mortality due to atherosclerotic cardiovascular disease. Familial hypercholesterolemia affects 1 in 200 to 250 p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=RECOLECTA___::02f2867a3320f79afe99cde908232413
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=2046
https://iibsantpau.fundanetsuite.com/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=2046
Autor:
Wilemon, KA, Patel, J, Aguilar-Salinas, C, Ahmed, CD, Alkhnifsawi, M, Almahmeed, W, Alonso, R, Al-Rasadi, K, Badimon, L, Bernal, LM, Bogsrud, MP, Braun, LT, Brunham, L, Catapano, AL, Cillíková, K, Corral, P, Cuevas, R, Defesche, JC, Descamps, OS, De Ferranti, S, Eiselé, J-L, Elikir, G, Folco, E, Freiberger, T, Fuggetta, F, Gaspar, IM, Gesztes, ÁG, Grošelj, U, Hamilton-Craig, I, Hanauer-Mader, G, Harada-Shiba, M, Hastings, G, Hovingh, GK, Izar, MC, Jamison, A, Karlsson, GN, Kayikçioglu, M, Koob, S, Koseki, M, Lane, S, Lima-Martinez, MM, López, G, Martinez, TL, Marais, D, Marion, L, Mata, P, Maurina, I, Maxwell, D, Mehta, R, Mensah, GA, Miserez, AR, Neely, D, Nicholls, SJ, Nohara, A, Nordestgaard, BG, Ose, L, Pallidis, A, Pang, J, Payne, J, Peterson, AL, Popescu, MP, Puri, R, Ray, KK, Reda, A, Sampietro, T, Santos, RD, Schalkers, I, Schreier, L, Shapiro, MD, Sijbrands, E, Soffer, D, Stefanutti, C, Stoll, M, Sy, RG, Tamayo, ML, Tilney, MK, Tokgözoglu, L, Tomlinson, B, Vallejo-Vaz, AJ, Vazquez-Cárdenas, A, De Luca, PV, Wald, DS, Watts, GF, Wenger, NK, Wolf, M, Wood, D, Zegerius, A, Gaziano, TA, Gidding, SS
Importance Familial hypercholesterolemia (FH) is an underdiagnosed and undertreated genetic disorder that leads to premature morbidity and mortality due to atherosclerotic cardiovascular disease. Familial hypercholesterolemia affects 1 in 200 to 250
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1032::4e6b2e513615db903a218c6cf941805c
http://hdl.handle.net/10044/1/78721
http://hdl.handle.net/10044/1/78721
Autor:
Alves, ST, Nepomuceno, LS, Bessa, AKM, Araújo, LMDSR, Santos, RD, Silva, ADG, Cruz, AC, Alves, ECF, Oliveira, JSR
Publikováno v:
In Hematology, Transfusion and Cell Therapy October 2022 44 Supplement 2:S500-S500
Autor:
Santos, RD, Gidding, SS, Hegele, RA, Cuchel, MA, Barter, PJ, Watts, GF, Baum, SJ, Catapano, AL, Chapman, MJ, Defesche, JC, Folco, E, Freiberger, T, Genest, J, Hovingh, GK, Harada-Shiba, M, Humphries, SE, Jackson, AS, Mata, P, Moriarty, PM, Raal, FJ, Al-Rasadi, K, Ray, KK, Reiner, Z, Sijbrands, EJ, Yamashita, S, International Atherosclerosis Society Severe Familial Hypercholesterolemia Panel
Publikováno v:
The Lancet Diabetes & Endocrinology, 4(10), 850-61. Elsevier
Familial hypercholesterolaemia is common in individuals who had a myocardial infarction at a young age. As many as one in 200 people could have heterozygous familial hypercholesterolaemia, and up to one in 300 000 individuals could be homozygous. The