Xin-guo Lu
Shenzhen, China
Last Updated: 09/26/2026
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Found 9 publications
Association of LONP1 gene with epilepsy and the sub-regional effect.
Journal: Scientific reports
Published: April 25, 2024
A Prospective Cohort Study on Quantitative Muscle Magnetic Resonance Imaging During the Treatment of Spinal Muscular Atrophy Types 2 and 3 in Children.
Journal: Pediatric neurology
Published: August 30, 2023
NEXMIF variants are associated with epilepsy with or without intellectual disability.
Journal: Seizure
Published: May 09, 2023
SZT2 variants associated with partial epilepsy or epileptic encephalopathy and the genotype-phenotype correlation.
Journal: Frontiers in molecular neuroscience
Published: February 09, 2023
Recessive PKD1 Mutations Are Associated With Febrile Seizures and Epilepsy With Antecedent Febrile Seizures and the Genotype-Phenotype Correlation.
Journal: Frontiers in molecular neuroscience
Published: January 24, 2022
Clinical features of sleep-disordered breathing in children with neuromuscular disease
Journal: Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics
Published: February 25, 2021
c.3G>A mutation in the CRYAB gene that causes fatal infantile hypertonic myofibrillar myopathy in the Chinese population.
Journal: Journal of integrative neuroscience
Published: September 05, 2020
Ketogenic diet poses a significant effect on imbalanced gut microbiota in infants with refractory epilepsy.
Journal: World journal of gastroenterology
Published: April 24, 2017
Showing 1-9 of 9
Last Updated: 09/26/2026