Virginie Verkarre

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

C. Junien, F. Brunelle, J. Saudubray, 1998, The Journal of clinical investigation.

Unbalanced expression of 11p15 imprinted genes in focal forms of congenital hyperinsulinism: association with a reduction to homozygosity of a mutation in ABCC8 or KCNJ11.

C. Junien, F. Brunelle, J. Saudubray, 2001, The American journal of pathology.

Refractory coeliac sprue is a diffuse gastrointestinal disease

E. Macintyre, N. Brousse, N. Cerf-Bensussan, 2003, Gut.

Chromosome 11p15 paternal isodisomy in focal forms of neonatal hyperinsulinism.

C. Bellanné-Chantelot, Y. Aigrain, P. de Lonlay, 2008, The Journal of clinical endocrinology and metabolism.