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Publications by C. M. MacMullen

Diazoxide-Unresponsive Congenital Hyperinsulinism in Children With Dominant Mutations of the -Cell Sulfonylurea Receptor SUR1

Internal Medicine

English

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Diazoxide-Unresponsive Congenital Hyperinsulinism Associated With ABCC8 Nonsense Mutation

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Transmembrane Topology of the Sulfonylurea Receptor SUR1

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Digenic Mutation Resulting in a Rare Form of Diazoxide Responsive Congenital Hyperinsulinism

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Diazoxide-Resistant Diffuse Hyperinsulinism

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In-Silico Study of Sulfonylurea Family Members’ Binding Site With Their Receptor Kir6.2\SUR1

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Hepatoblastoma and Wilms’ Tumour in an Infant With Beckwith–Wiedemann Syndrome and Diazoxide Resistant Congenital Hyperinsulinism

Endocrinology, Diabetes and Metabolism Case Reports

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Central Venous Catheter-Associated Thrombosis in Children With Congenital Hyperinsulinism

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Hyperinsulinism Caused by Paternal-Specific Inheritance of a Recessive Mutation in the Sulfonylurea-Receptor Gene

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Congenital Hyperinsulinism: Clinical and Molecular Characterisation of Compound Heterozygous ABCC8 Mutation Responsive to Diazoxide Therapy

International Journal of Pediatric Endocrinology

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