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Usefulness of the genetic risk score to identify phenocopies in families with familial hypercholesterolemia?
Ghaleb Y, Elbitar S, El Khoury P, Bruckert E, Carreau V, Carrié A, Moulin P, Di-Filippo M, Charriere S, Iliozer H, Farnier M, Luc G, Rabès JP, Boileau C, Abifadel M, Varret M. Ghaleb Y, et al. Among authors: bruckert e. Eur J Hum Genet. 2018 Apr;26(4):570-578. doi: 10.1038/s41431-017-0078-y. Epub 2018 Jan 26. Eur J Hum Genet. 2018. PMID: 29374275 Free PMC article.
[Dietetics of hypercholesterolemia].
Bruckert E. Bruckert E. Servir. 1999 May-Jun;47(3):122-6. Servir. 1999. PMID: 12035150 Portuguese. No abstract available.
Molecular spectrum of autosomal dominant hypercholesterolemia in France.
Marduel M, Carrié A, Sassolas A, Devillers M, Carreau V, Di Filippo M, Erlich D, Abifadel M, Marques-Pinheiro A, Munnich A, Junien C; French ADH Research Network; Boileau C, Varret M, Rabès JP. Marduel M, et al. Hum Mutat. 2010 Nov;31(11):E1811-24. doi: 10.1002/humu.21348. Hum Mutat. 2010. PMID: 20809525 Free PMC article.
Molecular analysis and intestinal expression of SAR1 genes and proteins in Anderson's disease (Chylomicron retention disease).
Georges A, Bonneau J, Bonnefont-Rousselot D, Champigneulle J, Rabès JP, Abifadel M, Aparicio T, Guenedet JC, Bruckert E, Boileau C, Morali A, Varret M, Aggerbeck LP, Samson-Bouma ME. Georges A, et al. Among authors: bruckert e. Orphanet J Rare Dis. 2011 Jan 14;6:1. doi: 10.1186/1750-1172-6-1. Orphanet J Rare Dis. 2011. PMID: 21235735 Free PMC article.
[Recommendations for hypercholesterolemic children].
Luc G, Girardet JP, Bruckert É, Rieu D, Farnier M, Darmaun D; Nouvelle Société Française d’Athérosclérose; Société Française de Pédiatrie. Luc G, et al. Among authors: bruckert e. Presse Med. 2011 Feb;40(2):138-50. doi: 10.1016/j.lpm.2010.12.001. Presse Med. 2011. PMID: 21391309 French.
464 results