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Journal Article
Diabetologia, ISSN 0012-186X, 3/2017, Volume 60, Issue 3, pp. 531 - 540
Journal Article
Clinical Endocrinology, ISSN 0300-0664, 05/2019, Volume 90, Issue 5, pp. 766 - 769
16p11.2 microdeletion syndrome is a recognisable chromosomal anomaly caused by microdeletions in the 16p11.2 locus. It is characterised by developmental delay,... 
hyperinsulinaemic hypoglycaemia | phenotype | Diazoxide | hypoketotic | 16p11.2 deletion syndrome | MICRODELETION | GENE | 16p11 | 2 deletion syndrome | ENDOCRINOLOGY & METABOLISM | Clonal deletion | Hypoglycemia
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 07/2019, Volume 91, Issue 3, pp. 216 - 220
Introduction: Post-prandial hyperinsulinaemic hypoglycaemia (PPHH) is a recognized complication of various gastric surgeries in children, but rarely reported... 
Novel Insights from Clinical Practice | REPAIR | MANAGEMENT | ATRESIA | ENDOCRINOLOGY & METABOLISM | PEDIATRICS | Oesophageal atresia | Dumping syndrome | DIAZOXIDE | Post-prandial hyperinsulinaemic hypoglycaemia | Hypertension | Acarbose | Laboratories | Fistulae | Fistula | Hypoglycemia | Insulin | Girls | Esophagus | Children & youth | Ostomy | Surgery | Children | Feeds | Seizures
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 2019, pp. 1 - 7
Initially described as an uncommon presenting feature of Sotos syndrome (SoS), over the last decades, congenital hyperinsulinaemic hypoglycaemia (CHI) has been... 
Liver dysfunction | Sotos syndrome | Congenital hyperinsulinaemic hypoglycaemia | Thrombosis | Rapid whole genome sequencing
Journal Article
Frontiers in Endocrinology, 03/2016, Volume 7
Under normal physiological conditions pancreatic β-cells secrete insulin to maintain fasting blood glucose levels in the range 3.5-5.5mmol/L. In... 
KATP Channels | congenital hyperinsulinism | Hyperinsulinaemic hypoglycaemia | Glucose | Insulin
Journal Article
Acta Paediatrica, ISSN 0803-5253, 10/2018, Volume 107, Issue 10, pp. 1759 - 1765
Journal Article
Hormone Research in Paediatrics, ISSN 1663-2818, 05/2019, Volume 91, Issue 1, pp. 56 - 61
Background: A long-acting somatostatin analogue (lanreotide) is used in the management of a diazoxide-unresponsive diffuse form of congenital hyperinsulinism... 
Novel Insights from Clinical Practice | Hyperinsulinaemic hypoglycaemia | ABCC8 gene | Somatostatin analogue | Lanreotide | Focal form | MANAGEMENT | MUTATION | ENDOCRINOLOGY & METABOLISM | PEDIATRICS
Journal Article
Journal of Pediatric Endocrinology and Metabolism, ISSN 0334-018X, 05/2015, Volume 28, Issue 5, pp. 695 - 699
Journal Article