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Research advances in diagnosis and treatment of hyperinsulinemia-hyperammonemia syndrome
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One case report of PCDH12 gene mutation-related epilepsy combined with severe development retardation，microcephalia and intracranial calcification
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Clinical phenotypes of epilepsy related to CHD2 gene mutations：A report of 18 patients
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Research progress in mitochondrial epilepsy in children
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Characteristics of the epilepsy classification by International League of Against Epilepsy and their interpretation
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Research progress in the pathogenic gene and clinical phenotype of epilepsy with myoclonic atonic seizures
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