Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management. - Wikidata - wikimedia - TriplyDB

Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

http://www.wikidata.org/entity/Q38049022

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Endocrine and metabolic complications after bariatric surgery The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia Hyperinsulinism in a neonate.Congenital hyperinsulinism: current status and future perspectives.Successful use of long acting octreotide in two cases with Beckwith-Wiedemann syndrome and severe hypoglycemia.Targeting SUR1/Abcc8-type neuroendocrine KATP channels in pancreatic islet cells.Hyperinsulinemic Hypoglycaemia in a Turner Syndrome with Ring (X).A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course.A novel mutation in GLUD1 causing hyperinsulinism-hyperammonemia in a patient with high density of homozygosity on microarray: a case report.Subtotal Pancreatectomy for Congenital Hyperinsulinism: Our Experience and Review of Literature Prematurity, macrosomia, hyperinsulinaemic hypoglycaemia and a dominant ABCC8 gene mutation.Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey.Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R.).Clinical practice guidelines for congenital hyperinsulinism.Congenital Hyperinsulinism in china: a review of Chinese literature over the past 15 years Development of Pulmonary Hypertension During Treatment with Diazoxide: A Case Series and Literature Review.Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients.Focal form of congenital hyperinsulinism clearly detectable by contrast-enhanced computed tomography imaging.A Multicenter Experience with Long-Acting Somatostatin Analogues in Patients with Congenital Hyperinsulinism.Population pharmacokinetics of exendin-(9-39) and clinical dose selection in patients with congenital hyperinsulinism.Polycystic Kidney Disease with Hyperinsulinemic Hypoglycemia Caused by a Promoter Mutation in Phosphomannomutase 2.Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann, Sotos, and Kabuki syndromes: A nationwide survey in Japan.

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P2860

Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

http://www.wikidata.org/entity/Q38049022

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Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

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Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

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Journal of clinical research in pediatric endocrinology

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Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.

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Khalid Hussain

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Ved Bhushan Arya

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Zainaba Mohamed

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Creative Commons Attribution 2.5 Unported

P2860

Mutation of the pancreatic islet inward rectifier Kir6.2 also leads to familial persistent hyperinsulinemic hypoglycemia of infancy

Clinical characteristics and biochemical mechanisms of congenital hyperinsulinism associated with dominant KATP channel mutations.

Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase

Physical exercise-induced hypoglycemia caused by failed silencing of monocarboxylate transporter 1 in pancreatic beta cells

Glucose induces closure of single potassium channels in isolated rat pancreatic beta-cells

A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor gene

Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene

Tissue-specific deletion of Foxa2 in pancreatic beta cells results in hyperinsulinemic hypoglycemia

Hyperinsulinism and Beckwith-Wiedemann syndrome

Hyperinsulinism in short-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency reveals the importance of beta-oxidation in insulin secretion

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169-181

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scholarly article

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10.4274/JCRPE.821

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4

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2012-10-02T00:00:00Z

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2012-12-01T00:00:00Z

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262041003

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23032149

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hyperinsulinemia

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3537282

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