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Page 1
Mutations in PCSK9 cause autosomal dominant hypercholesterolemia.
Abifadel M, Varret M, Rabès JP, Allard D, Ouguerram K, Devillers M, Cruaud C, Benjannet S, Wickham L, Erlich D, Derré A, Villéger L, Farnier M, Beucler I, Bruckert E, Chambaz J, Chanu B, Lecerf JM, Luc G, Moulin P, Weissenbach J, Prat A, Krempf M, Junien C, Seidah NG, Boileau C. Abifadel M, et al. Among authors: beucler i. Nat Genet. 2003 Jun;34(2):154-6. doi: 10.1038/ng1161. Nat Genet. 2003. PMID: 12730697
Magnitude of HDL cholesterol variation after high-dose atorvastatin is genetically determined at the LDL receptor locus in patients with homozygous familial hypercholesterolemia.
Sposito AC, Gonbert S, Bruckert E, Atassi M, Beucler I, Amsellem S, Khallouf O, Benlian P, Turpin G. Sposito AC, et al. Among authors: beucler i. Arterioscler Thromb Vasc Biol. 2003 Nov 1;23(11):2078-82. doi: 10.1161/01.ATV.0000097768.51278.91. Epub 2003 Sep 25. Arterioscler Thromb Vasc Biol. 2003. PMID: 14512370 Clinical Trial.
Genetic exclusion of apo-B gene in recessive abetalipoproteinemia.
Pessah M, Beucler I, Loux N, Navarro J, Guillerd X, Dulac O, Lequeux J, Junien C, Infante R. Pessah M, et al. Among authors: beucler i. Biochem Biophys Res Commun. 1993 Jan 15;190(1):97-103. doi: 10.1006/bbrc.1993.1016. Biochem Biophys Res Commun. 1993. PMID: 8422264
APOE: a potential marker of disease progression in ALS.
Lacomblez L, Doppler V, Beucler I, Costes G, Salachas F, Raisonnier A, Le Forestier N, Pradat PF, Bruckert E, Meininger V. Lacomblez L, et al. Among authors: beucler i. Neurology. 2002 Apr 9;58(7):1112-4. doi: 10.1212/wnl.58.7.1112. Neurology. 2002. PMID: 11940705
58 results