Jean‐Bernard Palcoux

Novel Paracellin-1 Mutations in 25 Families with Familial Hypomagnesemia with Hypercalciuria and Nephrocalcinosis

Stefanie Weber, Linda Schneider, Melanie Peters et al. · Journal of the American Society of Nephrology · 2001 · 269 citations

Long-term outcome of idiopathic steroid-resistant nephrotic syndrome: a multicenter study

Djalila Mekahli, A. Liutkus, Bruno Ranchin et al. · Pediatric Nephrology · 2009 · 206 citations

Glomerulonephritis, Urology, Renal Disease +7

Determination of the Genomic Structure of the COL4A4 Gene and of Novel Mutations Causing Autosomal Recessive Alport Syndrome

Eileen Boye, Géraldine Mollet, Lionel Forestier et al. · The American Journal of Human Genetics · 1998 · 140 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +9

Low‐density Lipoprotein Apheresis in Children With Familial Hypercholesterolemia: Follow‐up to 21 Years

Jean‐Bernard Palcoux, M Atassi-Dumont, Patrice Lefèvre et al. · Therapeutic Apheresis and Dialysis · 2008 · 63 citations · Full text

Hypertension, Vascular Disease, Genetic Epidemiology +22

A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with growth failure, lip/palate cleft(s), and urogenital anomalies

G Malpuech, F Deméocq, Jean‐Bernard Palcoux et al. · American Journal of Medical Genetics · 1983 · 51 citations