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Frontiers in Neurology|September 19, 2022
Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case reportHongmei Wang, Jiahong Li, Ji Zhou, et al.
Developmental Medicine and Child Neurology|July 15, 2021
Genotype-phenotype correlation of CACNA1A variants in children with epilepsyXueyang Niu, Ying Yang, Yi Chen, et al.
Developmental Medicine and Child Neurology|September 15, 2022
Clinical and genetic spectrum of hereditary spastic paraplegia in Chinese childrenJiaping Wang, Fang Fang, Changhong Ding, et al.
Frontiers in Pharmacology|October 25, 2021
Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers' Syndrome GenotypesHua Li, Wei Wang, Xiaodi Han, et al.
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