Aijie J. Liu
Beijing, China
Last Updated: 09/26/2026
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Found 27 publications
Genotypic spectrum in 1215 patients with Dravet syndrome or Dravet syndrome-like phenotype.
Journal: Pediatric research
Published: April 01, 2025
Research progress on DEPDC5 gene related epilepsy
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 01, 2022
PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency.
Journal: Frontiers in neurology
Published: September 11, 2022
Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing.
Journal: Journal of human genetics
Published: July 03, 2022
Seizure course of PCDH19 clustering epilepsy in female children: A multicentre cohort study in China.
Journal: Developmental medicine and child neurology
Published: April 06, 2022
Natural history and genetic study of LAMA2-related muscular dystrophy in a large Chinese cohort.
Journal: Orphanet journal of rare diseases
Published: May 07, 2021
Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy.
Journal: Neuromuscular disorders : NMD
Published: March 27, 2021
Clinical characteristics of PCDH19-female limited epilepsy
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 01, 2019
A phenotypic and genetic study on β-propeller protein-associated neurodegeneration
Journal: Zhonghua er ke za zhi = Chinese journal of pediatrics
Published: November 01, 2019
CHD2-related epilepsy: novel mutations and new phenotypes.
Journal: Developmental medicine and child neurology
Published: August 21, 2019
The clinical outcome and neuroimaging of acute encephalopathy after status epilepticus in Dravet syndrome.
Journal: Developmental medicine and child neurology
Published: January 24, 2018
Last Updated: 09/26/2026