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Genetics in endocrinology: genetic forms of severe insulin resistance: what endocrinologists should know.

Genetics in endocrinology: genetic forms of severe insulin resistance: what endocrinologists should know.

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How Useful Are Monogenic Rodent Models for the Study of Human Non-Alcoholic Fatty Liver Disease?Plasma Free Amino Acid Profiles Predict Four-Year Risk of Developing Diabetes, Metabolic Syndrome, Dyslipidemia, and Hypertension in Japanese Population Duration of Diabetes Predicts Aortic Pulse Wave Velocity and Vascular Events in Alström Syndrome.The 13C-Glucose Breath Test for Insulin Resistance Assessment in Adolescents: Comparison with Fasting and Post-Glucose Stimulus Surrogate Markers of Insulin Resistance Paediatric non-alcoholic fatty liver disease: a practical overview for non-specialists.Mecasermin in Insulin Receptor-Related Severe Insulin Resistance Syndromes: Case Report and Review of the Literature.Diagnostic and management challenges from childhood, puberty through to transition in severe insulin resistance due to insulin receptor mutations.The diagnosis and management of monogenic diabetes in children and adolescents

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Genetics in endocrinology: genetic forms of severe insulin resistance: what endocrinologists should know.

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2013 nî lūn-bûn

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2013 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

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2013 թվականի սեպտեմբերին հրատարակված գիտական հոդված

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2013年の論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年論文

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2013年论文

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European Journal of Endocrinology

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Genetics in endocrinology: gen ...... endocrinologists should know.

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Victoria E R Parker

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Familial hypertrophy of pineal body, hyperplasia of adrenal cortex and diabetes mellitus; report of 3 cases

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

Mutations in the pericentrin (PCNT) gene cause primordial dwarfism

Genetic Syndromes of Severe Insulin Resistance

The insulin-related ovarian regulatory system in health and disease.

Leptin reverses insulin resistance and hepatic steatosis in patients with severe lipodystrophy.

Genetic defects in human pericentrin are associated with severe insulin resistance and diabetes.

Clinical features and metabolic and autoimmune derangements in acquired partial lipodystrophy: report of 35 cases and review of the literature.

Acquired and inherited lipodystrophies.

Clinical features and metabolic derangements in acquired generalized lipodystrophy: case reports and review of the literature.

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R71-80

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10.1530/EJE-13-0327

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Robert K Semple

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