Pascale de Lonlay

Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia.

Virginie Verkarre, Jean‐Christophe Fournet, Pascale de Lonlay et al. · Journal of Clinical Investigation · 1998 · 290 citations · Full text

Medicine, Endocrinology, Genetics +17

<i>ABCC8</i> and <i>KCNJ11</i> molecular spectrum of 109 patients with diazoxide-unresponsive congenital hyperinsulinism

Christine Bellanné‐Chantelot, Cécile Saint‐Martin, Chantal Vaury et al. · Journal of Medical Genetics · 2010 · 118 citations

Life Sciences, Endocrinology, Genetics +17

Prevalence of the microdeletion 22q11 in newborn infants with congenital conotruncal cardiac anomalies

Laurence Iserin, Pascale de Lonlay, Géraldine Viot et al. · European Journal of Pediatrics · 1998 · 110 citations

Medicine, Cardiology, Pediatrics +16

Morphological Mosaicism of the Pancreatic Islets: A Novel Anatomopathological Form of Persistent Hyperinsulinemic Hypoglycemia of Infancy

Christine Sempoux, Carmen Capito, Christine Bellanné‐Chantelot et al. · The Journal of Clinical Endocrinology & Metabolism · 2011 · 98 citations · Full text

Medicine, Endocrinology, Pathology +17

Complement activation is a crucial driver of acute kidney injury in rhabdomyolysis

Idris Boudhabhay, Victoria Poillerat, Anne Grünenwald et al. · Kidney International · 2020 · 93 citations · Full text

Medicine, Immunology, Nephrology +16