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Hypothalamic atrophy of dentatorubral-pallidoluysian atrophy with epilepsy as the first symptom: A case report
[J]. Chinese Journal of Practical Pediatrics, 2021, 36(9): 706-709.
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Clinical features of epileptic encephalopathy caused by CASK gene variants
[J]. CJPP, 2021, 36(4): 275-280.
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One case of mental disorder combined with epilepsy caused by PPP2CA gene and the literature review
[J]. CJPP, 2021, 36(4): 318-320.
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Research advances in diagnosis and treatment of hyperinsulinemia-hyperammonemia syndrome
[J]. Chinese Journal of Practical Pediatrics, 2021, 36(10): 748-752.
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MO Ruo，YANG Yan-ling，ZHANG Yao.
Epilepsy as the main manifestation of inherited metabolic diseases
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ZHANG Ya-nan，ZHANG Hui-feng.
Congenital hyperinsulinemia misdiagnosed as epilepsy
[J]. CJPP, 2020, 35(7): 514-517.
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Phenotype and prognosis study of fifteen patients with late-onset Dravet syndrome
[J]. CJPP, 2020, 35(7): 557-561.
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One case report of PCDH12 gene mutation-related epilepsy combined with severe development retardation，microcephalia and intracranial calcification
[J]. CJPP, 2020, 35(7): 571-573.
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Wolf-Hirschhorn syndrome in one case and the literature review
[J]. CJPP, 2020, 35(7): 574-576.
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Analysis of age-dependent changes in routine immunological indicators of refractory Mycoplasma pneumoniae pneumonia in children
[J]. CJPP, 2020, 35(5): 373-378.
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Clinical phenotypes of epilepsy related to CHD2 gene mutations：A report of 18 patients
[J]. CJPP, 2020, 35(4): 289-294.
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HAN Xiao-di，FANG Fang.
Research progress in mitochondrial epilepsy in children
[J]. CJPP, 2020, 35(10): 805-811.
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Characteristics of the epilepsy classification by International League of Against Epilepsy and their interpretation
[J]. CJPP, 2020, 35(1): 47-54.
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WANG Hui-fang，SUN Mei-zhen.
Research progress in the pathogenic gene and clinical phenotype of epilepsy with myoclonic atonic seizures
[J]. CJPP, 2020, 35(1): 55-60.
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Expert consensus on the interventional diagnosis and treatment with respiratory endoscope in children with refractory pneumonia in China
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