P Vanlieferinghen

Deficiency of UBR1, a ubiquitin ligase of the N-end rule pathway, causes pancreatic dysfunction, malformations and mental retardation (Johanson-Blizzard syndrome)

Martin Zenker, Julia Mayerle, Markus M. Lerch et al. · Nature Genetics · 2005 · 270 citations

Protein Quality Control, Autoimmune Disease, Genetics +7

Antenatal detection and impact on outcome of congenital diaphragmatic hernia: A 12-year experience in Auvergne (France)

Denis Gallot, Karen Coste, Christine Francannet et al. · European Journal of Obstetrics & Gynecology and Reproductive Biology · 2005 · 88 citations

Antenatal Detection, Hernia Surgery, Congenital Diaphragmatic Hernia +4

Anti‐HPA‐9bw (Max^a) fetomaternal alloimmunization, a clinically severe neonatal thrombocytopenia: difficulties in diagnosis and therapy and report on eight families

Cécile Kaplan, Leendert Porcelijn, P Vanlieferinghen et al. · Transfusion · 2005 · 61 citations

Fetal umbilical cord ligation under ultrasound guidance

D. Lémery, P Vanlieferinghen, M. Gasq et al. · Ultrasound in Obstetrics and Gynecology · 1994 · 54 citations · Full text

Compromised Donor Fetus, Hydropic Recipient Twin, Ultrasound Guidance +13

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