Hyperinsulinism hyperammonaemia (HI/HA) syndrome due to GLUD1 mutation: phenotypic variations ranging from late presentation to spontaneous resolution

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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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The structure and allosteric regulation of mammalian glutamate dehydrogenase

(2011) Ming Li et al.   ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS

Congenital Hyperinsulinism due to a Compound Heterozygous ABCC8 Mutation with Spontaneous Resolution at Eight Weeks

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The hyperinsulinism/hyperammonemia syndrome

(2010) Andrew A. Palladino et al.   REVIEWS IN ENDOCRINE & METABOLIC DISORDERS

Neurological aspects of hyperinsulinism-hyperammonaemia syndrome

(2009) Nadia Bahi-Buisson et al.   DEVELOPMENTAL MEDICINE AND CHILD NEUROLOGY

Hyperinsulinism–hyperammonaemia syndrome: novel mutations in the GLUD1 gene and genotype–phenotype correlations

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