Ya Guo
No. 16 Jiangsu Road
Qingdao, 266000, China
Qingdao, 266000, China
Last Updated: 09/26/2026
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Found 22 publications
Glial fibrillary acidic protein astrocytopathy presented as meningitis: A case report.
Journal: Heliyon
Published: April 20, 2023
TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese children.
Journal: Immunity, inflammation and disease
Published: July 13, 2022
Two novel pathogenic mutations of GAN gene identified in a chinese family with giant axonal neuropathy: a case report.
Journal: Molecular biology reports
Published: February 15, 2022
Association of the IRAK4 rs4251545 genetic polymorphism with severity of enterovirus-71 infection in Chinese children.
Journal: Immunity, inflammation and disease
Published: December 28, 2021
Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene.
Journal: Journal of molecular neuroscience : MN
Published: October 31, 2019
Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: May 14, 2019
Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese Children.
Journal: Journal of molecular neuroscience : MN
Published: October 02, 2018
The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathy.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: April 01, 2018
A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: January 15, 2018
Gene analysis: A rare gene disease of intellectual deficiency-Cohen syndrome.
Journal: International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience
Published: January 12, 2018
Polymorphism of OAS2 rs739901 C/A Involves the Susceptibility to EV71 Infection in Chinese Children.
Polymorphism of OAS2 rs739901 C/A Involves the Susceptibility to EV71 Infection in Chinese Children.
Journal: Current medical science
Published: December 28, 2017
Last Updated: 09/26/2026