J.P. Van Biervliet

An Absence of Cutaneous Neurofibromas Associated with a 3-bp Inframe Deletion in Exon 17 of the NF1 Gene (c.2970-2972 delAAT): Evidence of a Clinically Significant NF1 Genotype-Phenotype Correlation

Meena Upadhyaya, Susan Huson, D. M. Davies et al. · The American Journal of Human Genetics · 2006 · 360 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetic Epidemiology +8

Catalytic triad residue mutation (Asp156—-Gly) causing familial lipoprotein lipase deficiency. Co-inheritance with a nonsense mutation (Ser447—-Ter) in a Turkish family

Fabrizia Faustinella, Anne M. Chang, J.P. Van Biervliet et al. · Journal of Biological Chemistry · 1991 · 116 citations · Full text

Family Members, Genetics, Molecular Biology +18

PLASMA APOPROTEIN AND LIPID PATTERNS IN NEWBORNS: INFLUENCE OF NUTRITIONAL FACTORS

J.P. Van Biervliet, N Vinaimont, Hans Caster et al. · Acta Paediatrica · 1981 · 66 citations

Oral DHA supplementation in ΔF508 homozygous cystic fibrosis patients

Stéphanie Van Biervliet, Michaël Devos, T. Delhaye et al. · Prostaglandins Leukotrienes and Essential Fatty Acids · 2008 · 59 citations

Fibrosis, Oral Dha Supplementation

EVOLUTION OF LIPOPROTEIN PATTERNS IN NEWBORNS

J.P. Van Biervliet, R. Vercaemst, W. De Keersgieter et al. · Acta Paediatrica · 1980 · 55 citations

Metabolic Syndrome, Lipid Disorder, Developmental Biology +15