Qiu-bo Li
Jining, China
Last Updated: 09/26/2026
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Found 8 publications
A GABRB3 mutation (c.5G>A, p.Trp2*) in twins with generalized epilepsy with febrile seizures: A case report.
Journal: Experimental and therapeutic medicine
Published: February 04, 2024
Multimodal Neuroimaging in Rett Syndrome With MECP2 Mutation.
Journal: Frontiers in neurology
Published: December 17, 2021
Two siblings suffering from Angelman Syndrome with a novel c.1146T>G mutation in UBE3A: A case report.
Journal: Biomedical reports
Published: April 19, 2021
Spatiotemporal Expression of SphK1 and S1PR2 in the Hippocampus of Pilocarpine Rat Model and the Epileptic Foci of Temporal Lobe Epilepsy.
Journal: Frontiers in cell and developmental biology
Published: March 22, 2020
Brain Proteomic Profiling in Intractable Epilepsy Caused by TSC1 Truncating Mutations: A Small Sample Study.
Journal: Frontiers in neurology
Published: March 05, 2020
Compound heterozygous mutations in the ALDH3A2 gene cause Sjögren-Larsson syndrome: a case report.
Journal: The International journal of neuroscience
Published: January 17, 2020
Paroxysmal spasticity of lower extremities as the initial symptom in two siblings with maple syrup urine disease.
Journal: Molecular medicine reports
Published: July 31, 2018
Showing 1-8 of 8
Last Updated: 09/26/2026