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Haolin Duan

Showing results (1-10 of 19) with videos related to

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Child Neurology Open|April 25, 2018
De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile SpasmsHaolin Duan, Jing Peng, Miriam Kessi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 6, 2024
MT-TN mutations lead to progressive mitochondrial encephalopathy and promotes mitophagyHaolin Duan, Cunhui Pan, Tenghui Wu, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|June 5, 2026
[<i>CNKSR2</i> gene variants causing Houge type of X-linked syndromic intellectual developmental disorder: Seven cases and literature review]Haolin Duan, Juan Xiong, Nan Pang, et al.
Child Neurology Open|September 29, 2018
A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication SyndromesMiriam Kessi, Jing Peng, Lifen Yang, et al.
Journal of Child Neurology|July 1, 2025
Application of High-Resolution Magnetic Resonance Vessel Wall Imaging in Childhood Primary Angiitis of the Central Nervous SystemZhanwei Zhang, Haolin Duan, Lifen Yang, et al.
BMC Genetics|July 7, 2018
Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic reviewMiriam Kessi, Jing Peng, Lifen Yang, et al.
Journal of Inflammation Research|October 9, 2025
Isolated Central Nervous System FHL3 in an Asian Pediatric Patient: A Case Report and Literature ReviewZhanwei Zhang, Haolin Duan, Ciliu Zhang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|January 11, 2020
[Application of ventricular shunt for children with post-infective hydrocephalus]Shimeng Chen, Jing Peng, Xiaolu Deng, et al.
BMC Medical Genomics|July 10, 2021
Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patientsJuan Xiong, Haolin Duan, Shimeng Chen, et al.
Frontiers in Pediatrics|January 24, 2022
Correlation Analyses of Clinical Manifestations and Variant Effects in <i>KCNB1</i>-Related Neurodevelopmental DisorderJuan Xiong, Zhonghua Liu, Shimeng Chen, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Child Neurology Open|April 25, 2018
De Novo KCNQ2 Mutation in One Case of Epilepsy of Infancy With Migrating Focal Seizures That Evolved to Infantile SpasmsHaolin Duan, Jing Peng, Miriam Kessi, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|February 6, 2024
MT-TN mutations lead to progressive mitochondrial encephalopathy and promotes mitophagyHaolin Duan, Cunhui Pan, Tenghui Wu, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|June 5, 2026
[<i>CNKSR2</i> gene variants causing Houge type of X-linked syndromic intellectual developmental disorder: Seven cases and literature review]Haolin Duan, Juan Xiong, Nan Pang, et al.
Child Neurology Open|September 29, 2018
A Case With 4 de Novo Copy Number Variations With Clinical Features That Overlap 1q43q44 Microdeletion and 3q29 Microduplication SyndromesMiriam Kessi, Jing Peng, Lifen Yang, et al.
Journal of Child Neurology|July 1, 2025
Application of High-Resolution Magnetic Resonance Vessel Wall Imaging in Childhood Primary Angiitis of the Central Nervous SystemZhanwei Zhang, Haolin Duan, Lifen Yang, et al.
BMC Genetics|July 7, 2018
Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic reviewMiriam Kessi, Jing Peng, Lifen Yang, et al.
Journal of Inflammation Research|October 9, 2025
Isolated Central Nervous System FHL3 in an Asian Pediatric Patient: A Case Report and Literature ReviewZhanwei Zhang, Haolin Duan, Ciliu Zhang, et al.
Zhong Nan Da Xue Xue Bao. Yi Xue Ban = Journal of Central South University. Medical Sciences|January 11, 2020
[Application of ventricular shunt for children with post-infective hydrocephalus]Shimeng Chen, Jing Peng, Xiaolu Deng, et al.
BMC Medical Genomics|July 10, 2021
Familial SYN1 variants related neurodevelopmental disorders in Asian pediatric patientsJuan Xiong, Haolin Duan, Shimeng Chen, et al.
Frontiers in Pediatrics|January 24, 2022
Correlation Analyses of Clinical Manifestations and Variant Effects in <i>KCNB1</i>-Related Neurodevelopmental DisorderJuan Xiong, Zhonghua Liu, Shimeng Chen, et al.
Pageof 2