Disease: Hyperinsulinism due to focal adenomatous hyperplasia
- Acute insulin responses to calcium and tolbutamide do not differentiate focal from diffuse congenital hyperinsulinism
- Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy
- Characterization of hyperinsulinism in infancy assessed with PET and 18F-fluoro-L-DOPA
- Clinical features of 52 neonates with hyperinsulinism
- Congenital hyperinsulinism
- Congenital hyperinsulinism: intraoperative biopsy interpretation can direct the extent of pancreatectomy
- Cure of hypoglycemic hyperinsulinism by enucleation of a focal islet cell adenomatous hyperplasia
- Facial appearance in persistent hyperinsulinemic hypoglycemia
- Functional imaging of the pancreas: the role of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy
- Genotype-histotype-phenotype correlations in hyperinsulinemic hypoglycemia
- Heterogeneity of persistent hyperinsulinaemic hypoglycaemia. A series of 175 cases
- Identification of two novel frameshift mutations in the KCNJ11 gene in two Italian patients affected by Congenital Hyperinsulinism of Infancy
- Laparoscopic diagnosis and cure of hyperinsulinism in two cases of focal adenomatous hyperplasia in infancy
- Loss of imprinted genes and paternal SUR1 mutations lead to hyperinsulinism in focal adenomatous hyperplasia
- Molecular and immunohistochemical analyses of the focal form of congenital hyperinsulinism
- Molecular mechanisms of neonatal hyperinsulinism
- Neonatal hyperinsulinemic hypoglycemia: heterogeneity of the syndrome and keys for differential diagnosis
- Neurologic outcomes of 90 neonates and infants with persistent hyperinsulinemic hypoglycemia
- p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy
- Pancreatic adenomatous hyperplasia and sudden infant death
- Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy
- Pancreatic B-cell proliferation in persistent hyperinsulinemic hypoglycemia of infancy: an immunohistochemical study of 18 cases
- Partial or near-total pancreatectomy for persistent neonatal hyperinsulinaemic hypoglycaemia: the pathologist's role
- Paternal mutation of the sulfonylurea receptor (SUR1) gene and maternal loss of 11p15 imprinted genes lead to persistent hyperinsulinism in focal adenomatous hyperplasia
- Persistent hyperinsulinemic hypoglycemia of infancy
- Persistent neonatal hyperinsulinism. Analysis of the differential diagnosis. Report of two cases
- Somatic deletion of the imprinted 11p15 region in sporadic persistent hyperinsulinemic hypoglycemia of infancy is specific of focal adenomatous hyperplasia and endorses partial pancreatectomy
- The added value of [18F]fluoro-L-DOPA PET in the diagnosis of hyperinsulinism of infancy: a retrospective study involving 49 children
- The Knudson's two-hit model and timing of somatic mutation may account for the phenotypic diversity of focal congenital hyperinsulinism
- Three novel pathogenic mutations in KATP channel genes and somatic imprinting alterations of the 11p15 region in pancreatic tissue in patients with congenital hyperinsulinism
- 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
- Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels