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Results:
1-8
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Results: 8
Authors:
Benlian, P
Citation: P. Benlian, Familial hypercholesterolemia: Genetic causes and risks in adulthood, ARCH PED, 8, 2001, pp. 511S-512S
Authors:
Viola, S
Benlian, P
Morali, A
Dobbelaere, D
Lacaille, F
Rieu, R
Ginies, EL
Maurage, C
Meyer, M
Lachaux, T
Larchet, M
Lenearts, C
Goulet, O
Sarles, J
Mouterde, O
Girardet, JP
Citation: S. Viola et al., Apolipoprotein B Arg3500Gln mutation prevalence in children with hypercholesterolemia: A French multicenter study, J PED GASTR, 33(2), 2001, pp. 122-126
Authors:
Corpechot, C
Benlian, P
Barbu, V
Chazouilleres, O
Poupon, RE
Poupon, R
Citation: C. Corpechot et al., Apolipoprotein E polymorphism, a marker of disease severity in primary biliary cirrhosis?, J HEPATOL, 35(3), 2001, pp. 324-328
Authors:
Slimane, MN
Lestavel, S
Sun, XM
Maatouk, F
Soutar, AK
Ben Farhat, MH
Clavey, V
Benlian, P
Hammami, M
Citation: Mn. Slimane et al., Fh-Souassi: a founder frameshift mutation in exon 10 of the LDL-receptor gene, associated with a mild phenotype in Tunisian families, ATHEROSCLER, 154(3), 2001, pp. 557-565
Authors:
Benlian, P
Citation: P. Benlian, Recent advances and new tools in the study of molecular genetics of lipoprotein disorders, B ACA N MED, 185(1), 2001, pp. 21-33
Authors:
Benlian, P
Cansier, C
Hennache, G
Khallouf, O
Bayer, P
Duron, F
Carrat, F
Couderc, R
Chazouilleres, O
Bardet, J
Bouchard, P
Poupon, R
Masliah, J
Bereziat, G
Citation: P. Benlian et al., Comparison of a new method for the direct and simultaneous assessment of LDL- and HDL-cholesterol with ultracentrifugation and established methods, CLIN CHEM, 46(4), 2000, pp. 493-505
Authors:
Frenais, R
Ouguerram, K
Maugeais, C
Marchini, JS
Benlian, P
Bard, JM
Magot, T
Krempf, M
Citation: R. Frenais et al., Apolipoprotein A-I kinetics in heterozygous familial hypercholesterolemia:a stable isotope study, J LIPID RES, 40(8), 1999, pp. 1506-1511
Authors:
Teh, EM
Chisholm, JW
Dolphin, PJ
Pouliquen, Y
Savoldelli, M
de Gennes, JL
Benlian, P
Citation: Em. Teh et al., Classical LCAT deficiency resulting from a novel homozygous dinucleotide deletion in exon 4 of the human lecithin: cholesterol acyltransferase gene causing a frameshift and stop codon at residue 144, ATHEROSCLER, 146(1), 1999, pp. 141-151
Risultati:
1-8
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