✦ LIBER ✦

T07-P-004 Phenotype comparison in children with familial defective apolipoprotein B and familial hypercholesterolemia

✍ Scribed by Grombuikova, H.; Kopalkova, L.; Urbanova, Z.; Samanek, M.; Kuhrova, V.; Kozak, L.; Freiberger, T.

Book ID: 118633751
Publisher: Elsevier Science
Year: 2005
Tongue: English
Weight: 135 KB
Volume: 6
Category: Article
ISSN: 1567-5688
DOI: 10.1016/s1567-5688(05)80670-1

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Comparison of apolipoprotein B metabolis

Comparison of apolipoprotein B metabolism in familial defective apolipoprotein B and heterogeneous familial hypercholesterolemia

✍ Dairena Gaffney; Lorne Forster; Muriel J. Caslake; Dorothy Bedford; J.Philip Ste 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 144 KB

98 Familial hypercholesterolemia and fam

98 Familial hypercholesterolemia and familial defective apolipoprotein B in Belgium

✍ O. Descamps; J-C Hondekijn; P. Vanacker; J-P Deslypere; F.R. Heller 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 152 KB

Phenotypic expression in double heterozy

Phenotypic expression in double heterozygotes for familial hypercholesterolemia and familial defective apolipoprotein B-100

✍ Pascale Benlian; Jean Luc de Gennes; François Dairou; Brigitte Hermelin; Isabell 📂 Article 📅 1996 🏛 John Wiley and Sons 🌐 English ⚖ 554 KB

## Communicated by Michel Goossens Variability in the expression of monogenic lipid disorders may be observed in patients carrying the same DNA mutation, suggesting possible genetic or environmental interactions. Our objective was to investigate the genotype-phenotype relationships in two unrelate

Lipid levels and their genetic regulatio

Lipid levels and their genetic regulation in patients with familial hypercholesterolemia and familial defective apolipoprotein B-100: the MEDPED Slovakia Project

✍ Vohnout, B 📂 Article 📅 2003 🏛 Elsevier Science 🌐 English ⚖ 51 KB

1.P.258 Mutation screening in patients w

1.P.258 Mutation screening in patients with a phenotype of familial hypercholesterolemia and normal values in a functional LDL receptor/apolipoprotein B assay

✍ H. Nissen; S. Lestavel; T.S. Hansen; G. Luc; E. Bruckert; V. Clavey 📂 Article 📅 1997 🏛 Elsevier Science 🌐 English ⚖ 195 KB

Absence of familial defective apolipopro

Absence of familial defective apolipoprotein B-100 in Israeli patients with dominantly inherited hypercholesterolemia and in offspring with parental history of myocardial infarction

✍ Yechiel Friedlander; Eldad J. Dann; Eran Leitersdorf 📂 Article 📅 1993 🏛 Springer 🌐 English ⚖ 200 KB