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Publications by YueHua Zhang
Gene Mutational Analysis in a Cohort of Chinese Children With Unexplained Epilepsy:identification of a New KCND3 Phenotype and Novel Genes Causing Dravet Syndrome
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
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A Novel Homozygous Truncating Mutation in LAMB2 Gene in a Chinese Uyghur Patient With Severe Phenotype Pierson Syndrome
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A Novel Mutation in ERCC8 Gene Causing Cockayne Syndrome
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Quality of Life and Comorbidities Associated With Dravet Syndrome Severity: A Multinational Cohort Survey
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Unexpected Efficacy of a Novel Sodium Channel Modulator in Dravet Syndrome
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Large-Scale Phenotype-Based Antiepileptic Drug Screening in a Zebrafish Model of Dravet Syndrome
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B Cell Subsets Phenotype in Autoimmunity With Immunodeficiency: Analysis of a Cohort of Patients With APECED Syndrome
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A New Mutation in IDS Gene Causing Hunter Syndrome: A Case Report
Frontiers in Genetics
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Mutational Analysis of the MECP2 Gene in Japanese Patients With Rett Syndrome
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A Novel Indicator of Lipid Accumulation Product Associated With Metabolic Syndrome in Chinese Children and Adolescents
Diabetes, Metabolic Syndrome and Obesity: Targets and Therapy
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