Marion Gérard‐Blanluet

Alternating Hemiplegia of Childhood: Early Characteristics and Evolution of a Neurodevelopmental Syndrome

Matthew Sweney, Kenneth Silver, Marion Gérard‐Blanluet et al. · PEDIATRICS · 2009 · 145 citations

CNS malformations in Knobloch syndrome with splice mutation in <i>COL18A1</i> gene

Boris Keren, Oscar Suzuki, Marion Gérard‐Blanluet et al. · American Journal of Medical Genetics Part A · 2007 · 40 citations

Developmental Anomaly, Cns Malformations, Genetic Disorder +11

Binder phenotype: clinical and etiological heterogeneity of the so‐called Binder maxillonasal dysplasia in prenatally diagnosed cases, and review of the literature

J. M. Levaillant, D. Moeglin, K. Zouiten et al. · Prenatal Diagnosis · 2009 · 37 citations

Specific osseous spurs in a lethal form of hypophosphatasia correlated with 3D prenatal ultrasonographic images

M Sinico, J. M. Levaillant, A. Vergnaud et al. · Prenatal Diagnosis · 2007 · 32 citations

CEMARA an information system for rare diseases

Paul Landais, Claude Messiaen, Ana Rath et al. · Studies in health technology and informatics · 2010 · 32 citations

Engineering, Labelled Reference Centres, Information System +19