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Pediatric Neurology|April 22, 2009
Benign familial neonatal convulsions: novel mutation in a newbornInn-Chi Lee, Jia-Yuh Chen, Yung-Jung Chen, et al.Scientific Reports|August 10, 2020
Heteromeric Kv7.2 current changes caused by loss-of-function of KCNQ2 mutations are correlated with long-term neurodevelopmental outcomesInn-Chi Lee, Jiann-Jou Yang, Swee-Hee Wong, et al.Frontiers in Pediatrics|November 22, 2019
Infants of Mothers With Diabetes and Subsequent Attention Deficit Hyperactivity Disorder: A Retrospective Cohort StudyChien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire|July 20, 2022
Effects of aldo-keto reductase family 1 member A on osteoblast differentiation associated with lactate production in MC3T3-E1 preosteoblastic cellsChia-Hsiao Kuo, Inn-Chi Lee, Bo-Jun Huang, et al.Channels (Austin, Tex.)|February 19, 2025
Biophysical and structural mechanisms of epilepsy-associated mutations in the S4-S5 Linker of KCNQ2 channelsInn-Chi Lee, Yen-Yu Yang, Hsueh-Kai Chang, et al.CNS & Neurological Disorders Drug Targets|June 1, 2026
KCNQ2 Channel as a Druggable Epilepsy Target: Advances in Pharmacological ModifiersInn-Chi Lee, Shi-Bing Yang, Swee-Hee Wong, et al.BMC Pediatrics|November 6, 2019
Heterogeneous neurodevelopmental disorders in children with Kawasaki disease: what is new today?Chien-Heng Lin, Wei-De Lin, I-Ching Chou, et al.Journal of Child Neurology|April 13, 2017
KCNQ2-Associated Neonatal Epilepsy: Phenotype Might Correlate With GenotypeInn-Chi Lee, Jiann-Jou Yang, Jao-Shwann Liang, et al.Pediatrics and Neonatology|June 28, 2011
Interstitial deletions of the short arm of chromosome 4 in a patient with mental retardation and focal seizurePen-Hua Su, Inn-Chi Lee, Jia-Yuh Chen, et al.Pediatrics and Neonatology|November 1, 2011
Common etiologies of neonatal pleural effusionYueh-Ting Shih, Pen-Hua Su, Jia-Yuh Chen, et al.Pageof 6