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Etiology and prognosis of acute viral encephalitis and meningitis in Chinese children: a multicentre prospective study

BMC infectious diseases, 2017-07, Vol.17 (1), p.494-494, Article 494

2017

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Correlation between TLR4 gene polymorphism and severe enterovirus 71 infection

Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2020-10, Vol.26 (10), p.1015-1020

2020

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Ameliorative effect of synthesized silver nanoparticles by green route method from Zingiber zerumbet on mycoplasmal pneumonia in experimental mice

Artificial cells, nanomedicine, and biotechnology, 2019-12, Vol.47 (1), p.2146-2154

2019

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Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report

BMC medical genetics, 2018-06, Vol.19 (1), p.92-92, Article 92

2018

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TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese children

Immunity, Inflammation and Disease, 2022-12, Vol.10 (12), p.e742-n/a

2022

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Association of the IRAK4 rs4251545 genetic polymorphism with severity of enterovirus‐71 infection in Chinese children

Immunity, Inflammation and Disease, 2022-05, Vol.10 (5), p.e614-n/a

2022

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Reduced pericyte and tight junction coverage in old diabetic rats are associated with hyperglycemia-induced cerebrovascular pericyte dysfunction

American journal of physiology. Heart and circulatory physiology, 2021-02, Vol.320 (2), p.H549-H562

2021

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Association of CD14 rs2569190 G/A genetic polymorphism with the severity of enterovirus 71 infection in Chinese children

Virology (New York, N.Y.), 2020-09, Vol.548, p.25-30

2020

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Correlation between TICAM1 gene polymorphisms and community‐acquired pneumonia in children

Journal of biochemical and molecular toxicology, 2020-08, Vol.34 (8), p.e22503-n/a

2020

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Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases

International journal of developmental neuroscience, 2021-02, Vol.81 (1), p.98-105

2021

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Three Novel ARID1B Variations in Coffin-Siris Syndrome Patients

Neurology India, 2022-09, Vol.70 (5), p.2174

2022

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Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children

International journal of developmental neuroscience, 2019-11, Vol.78 (1), p.28-32

2019

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20-HETE-promoted cerebral blood flow autoregulation is associated with enhanced pericyte contractility

Prostaglandins & other lipid mediators, 2021-06, Vol.154, p.106548-106548, Article 106548

2021

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Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

Molecular neurodegeneration, 2018-08, Vol.13 (1), p.41-41, Article 41

2018

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Association of the OAS3 rs1859330 G/A genetic polymorphism with severity of enterovirus-71 infection in Chinese Han children

Archives of virology, 2017-08, Vol.162 (8), p.2305-2313

2017

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A case of TSC2‐PKD1 contiguous deletion syndrome: Clinical features and effective treatment for epilepsy

International journal of developmental neuroscience, 2021-04, Vol.81 (2), p.191-199

2021

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Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese Children

Journal of molecular neuroscience, 2019-10, Vol.69 (2), p.188-196

2019

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Association of Interleukin-17F gene polymorphisms with susceptibility to severe enterovirus 71 infection in Chinese children

Archives of virology, 2018-07, Vol.163 (7), p.1933-1939

2018

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Oligoadenylate synthetase 3 S381R gene polymorphism is associated with severity of EV71 infection in Chinese children

Journal of clinical virology, 2018-04, Vol.101, p.29-33

2018

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Gene analysis: A rare gene disease of intellectual deficiency-Cohen syndrome

International journal of developmental neuroscience, 2018-08, Vol.68 (1), p.83-88

2018

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The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathy

International journal of developmental neuroscience, 2018-12, Vol.71 (1), p.172-174

2018

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Impact of IL-8-251A/T gene polymorphism on severity of disease caused by enterovirus 71 infection

Archives of virology, 2016-01, Vol.161 (1), p.203-207

2016

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A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy

International journal of developmental neuroscience, 2018-06, Vol.67 (1), p.51-54

2018

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Carnitine palmitoyl transferase 2 polymorphism may be associated with enterovirus 71 severe infection in a Chinese population

Archives of virology, 2016-05, Vol.161 (5), p.1217-1227

2016

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Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene

Journal of molecular neuroscience, 2021-02, Vol.71 (2), p.245-251

2021

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Etiology and prognosis of acute viral encephalitis and meningitis in Chinese children: a multicentre prospective study

Correlation between TLR4 gene polymorphism and severe enterovirus 71 infection

Ameliorative effect of synthesized silver nanoparticles by green route method from Zingiber zerumbet on mycoplasmal pneumonia in experimental mice

Chinese cases of early infantile epileptic encephalopathy: a novel mutation in the PCDH19 gene was proved in a mosaic male- case report

TMEM173 rs7447927 genetic polymorphism and susceptibility to severe enterovirus 71 infection in Chinese children

Association of the IRAK4 rs4251545 genetic polymorphism with severity of enterovirus‐71 infection in Chinese children

Reduced pericyte and tight junction coverage in old diabetic rats are associated with hyperglycemia-induced cerebrovascular pericyte dysfunction

Association of CD14 rs2569190 G/A genetic polymorphism with the severity of enterovirus 71 infection in Chinese children

Correlation between TICAM1 gene polymorphisms and community‐acquired pneumonia in children

Novel variants in TBC1D24 associated with epilepsy and deafness: Report of two cases

Three Novel ARID1B Variations in Coffin-Siris Syndrome Patients

Levodopa is effective in the treatment of three Chinese Tyrosine hydroxylase (TH) deficiency children

20-HETE-promoted cerebral blood flow autoregulation is associated with enhanced pericyte contractility

Joint genome-wide association study of progressive supranuclear palsy identifies novel susceptibility loci and genetic correlation to neurodegenerative diseases

Association of the OAS3 rs1859330 G/A genetic polymorphism with severity of enterovirus-71 infection in Chinese Han children

A case of TSC2‐PKD1 contiguous deletion syndrome: Clinical features and effective treatment for epilepsy

Association of the Polymorphism of rs1799822 on Carnitine Palmitoyltransferase II Gene with Severe Enterovirus 71 Encephalitis in Chinese Children

Association of Interleukin-17F gene polymorphisms with susceptibility to severe enterovirus 71 infection in Chinese children

Oligoadenylate synthetase 3 S381R gene polymorphism is associated with severity of EV71 infection in Chinese children

Gene analysis: A rare gene disease of intellectual deficiency-Cohen syndrome

The biochemical characterization of a missense mutation m.8914C>T in ATP6 gene associated with mitochondrial encephalomyopathy

Impact of IL-8-251A/T gene polymorphism on severity of disease caused by enterovirus 71 infection

A case of Pitt-hopkins Syndrome with de novo mutation in TCF4: Clinical features and treatment for epilepsy

Carnitine palmitoyl transferase 2 polymorphism may be associated with enterovirus 71 severe infection in a Chinese population

Chinese Cases of Metachromatic Leukodystrophy with the Novel Missense Mutations in ARSA Gene

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