Congenital hyperinsulinism: current trends in diagnosis and therapy. - Wikidata - wikimedia - TriplyDB

Congenital hyperinsulinism: current trends in diagnosis and therapy.

Congenital hyperinsulinism: current trends in diagnosis and therapy.

http://www.wikidata.org/entity/Q37941900

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Therapeutic Approaches to Genetic Ion Channelopathies and Perspectives in Drug Discovery Long-term medical treatment in congenital hyperinsulinism: a descriptive analysis in a large cohort of patients from different clinical centers The Diagnosis and Management of Hyperinsulinaemic Hypoglycaemia Clinical review of genetic epileptic encephalopathies Congenital hyperinsulinism in Chinese patients: 5-yr treatment outcome of 95 clinical cases with genetic analysis of 55 cases.Update on neonatal hypoglycemia.Vineland adaptive behavior scales to identify neurodevelopmental problems in children with Congenital Hyperinsulinism (CHI).Congenital hyperinsulinism: current status and future perspectives.Evaluation of mild hypothermia therapy for neonatal hypoxic-ischaemic encephalopathy on brain energy metabolism using (18)F-fluorodeoxyglucose positron emission computed tomography.Uncoupling of secretion from growth in some hormone secretory tissues.Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.Surgical management of congenital hyperinsulinism in a resource-limited setting.A liquid chromatography-mass spectrometry assay for quantification of Exendin[9-39] in human plasma.Drug-induced hepatitis following use of octreotide for long-term treatment of congenital hyperinsulinism.Nifedipine in Congenital Hyperinsulinism - A Case Report.The value of radiologic interventions and (18)F-DOPA PET in diagnosing and localizing focal congenital hyperinsulinism: systematic review and meta-analysis Subtotal Pancreatectomy for Congenital Hyperinsulinism: Our Experience and Review of Literature Monogenic Diabetes: What It Teaches Us on the Common Forms of Type 1 and Type 2 Diabetes.Enhanced Islet Cell Nucleomegaly Defines Diffuse Congenital Hyperinsulinism in Infancy but Not Other Forms of the Disease Multiplicity of hormone-secreting tumors: common themes about cause, expression, and management.Hyperinsulinemic hypoglycemia: experience in a series of 17 cases Persistent Hyperinsulinism in Kabuki Syndrome 2: Case Report and Literature Review Conservatively treated Congenital Hyperinsulinism (CHI) due to K-ATP channel gene mutations: reducing severity over time.Reduced Glycemic Variability in Diazoxide-Responsive Children with Congenital Hyperinsulinism Using Supplemental Omega-3-Polyunsaturated Fatty Acids; A Pilot Trial with MaxEPA(R.).Diagnostic performance of fluorine-18-dihydroxyphenylalanine positron emission tomography in diagnosing and localizing the focal form of congenital hyperinsulinism: a meta-analysis.Hyperinsulinaemic hypoglycaemia:genetic mechanisms, diagnosis and management.Integrating genetic and imaging investigations into the clinical management of congenital hyperinsulinism.Abnormal Neurodevelopmental Outcomes are Common in Children with Transient Congenital Hyperinsulinism.Selective allosteric antibodies to the insulin receptor for the treatment of hyperglycemic and hypoglycemic disorders.Congenital hyperinsulinism: Role of fluorine-18L-3, 4 hydroxyphenylalanine positron emission tomography scanning.Feeding Problems Are Persistent in Children with Severe Congenital Hyperinsulinism.Fatal congenital hypertrophic cardiomyopathy and a pancreatic nodule morphologically identical to focal lesion of congenital hyperinsulinism in an infant with costello syndrome: case report and review of the literature.Clinical practice guidelines for congenital hyperinsulinism.Recognition, assessment and management of hypoglycaemia in childhood.Development of Pulmonary Hypertension During Treatment with Diazoxide: A Case Series and Literature Review.Hyperinsulinemic hypoglycemia: clinical, molecular and therapeutical novelties.A Novel Homozygous Mutation in the KCNJ11 Gene of a Neonate with Congenital Hyperinsulinism and Successful Management with Sirolimus.Both Low Blood Glucose and Insufficient Treatment Confer Risk of Neurodevelopmental Impairment in Congenital Hyperinsulinism: A Multinational Cohort Study Can network biology unravel the aetiology of congenital hyperinsulinism?Diagnosis and treatment of hyperinsulinaemic hypoglycaemia and its implications for paediatric endocrinology.

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P2860

Congenital hyperinsulinism: current trends in diagnosis and therapy.

http://www.wikidata.org/entity/Q37941900

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Congenital hyperinsulinism: current trends in diagnosis and therapy.

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Anaïs Brassier

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Cécile Saint-Martin

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

Glucagon receptors on human islet cells contribute to glucose competence of insulin release

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

Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism

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

Brief report: impaired processing of prohormones associated with abnormalities of glucose homeostasis and adrenal function

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

Macrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A gene

The MODY1 gene HNF-4alpha regulates selected genes involved in insulin secretion.

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Vassili Valayannopoulos

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