Familial hypercholesterolaemia: a global call to arms

Familial Hypercholesterolaemia (FH) is the commonest autosomal co-dominantly inherited condition affecting man. It is caused by mutation in one of three genes, encoding the low-density lipoprotein (LDL) receptor, or the gene for apolipoprotein B (which is the major protein component of the LDL parti...

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Detalhes bibliográficos
Autor principal: Vallejo-Vaz, A.J. (author)
Outros Autores: Kondapally Seshasai, S.R. (author), Cole, D. (author), Hovingh, G.K. (author), Kastelein, J.J. (author), Mata, P. (author), Raal, F.J. (author), Santos, R.D. (author), Soran, H. (author), Watts, G.F. (author), Abifadel, M. (author), Aguilar-Salinas, C.A. (author), Akram, A. (author), Alnouri, F. (author), Alonso, R. (author), Al-Rasadi, K. (author), Banach, M. (author), Bogsrud, M.P. (author), Bourbon, M. (author), Bruckert, E. (author), Car, J. (author), Corral, P. (author), Descamps, O. (author), Dieplinger, H. (author), Durst, R. (author), Freiberger, T. (author), Gaspar, I.M. (author), Genest, J. (author), Harada-Shiba, M. (author), Jiang, L. (author), Kayikcioglu, M. (author), Lam, C.S. (author), Latkovskis, G. (author), Laufs, U. (author), Liberopoulos, E. (author), Nilsson, L. (author), Nordestgaard, B.G. (author), O'Donoghue, J.M. (author), Sahebkar, A. (author), Schunkert, H. (author), Shehab, A. (author), Stoll, M. (author), Su, TC (author), Susekov, A. (author), Widén, E. (author), Catapano, A.L. (author), Ray, K.K. (author)
Formato: article
Idioma:eng
Publicado em: 2015
Assuntos:
Familial Hypercholesterolaemia
Doenças Cardio e Cérebro-vasculares
Texto completo:http://hdl.handle.net/10400.18/3174
País:Portugal
Oai:oai:repositorio.insa.pt:10400.18/3174

Texto Completo

http://hdl.handle.net/10400.18/3174

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