Hongliang Xu

No. 1 Jianshe East Road
Zhengzhou, 450052, China

Last Updated: 09/26/2026

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Found 16 publications

Magnetic resonance imaging changes of thigh muscles in dermatomyositis patients with anti-Mi2 antibody.

Magnetic resonance imaging changes of thigh muscles in dermatomyositis patients with anti-Mi2 antibody.

Journal: Annals of medicine

Published: August 01, 2026

Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane.

Novel mutations in ATP7B in Chinese patients with Wilson's disease and identification of kidney disorder of thinning of the glomerular basement membrane.

Journal: Frontiers in neurology

Published: May 30, 2023

The Noninvasive Sonothermogenetics Used for Neuromodulation in M1 Region of Mice Brain by Overexpression of TRPV1.

The Noninvasive Sonothermogenetics Used for Neuromodulation in M1 Region of Mice Brain by Overexpression of TRPV1.

Journal: Neuroscience

Published: February 26, 2023

Interaction between TRPML1 and p62 in Regulating Autophagosome-Lysosome Fusion and Impeding Neuroaxonal Dystrophy in Alzheimer's Disease.

Interaction between TRPML1 and p62 in Regulating Autophagosome-Lysosome Fusion and Impeding Neuroaxonal Dystrophy in Alzheimer's Disease.

Journal: Oxidative medicine and cellular longevity

Published: July 29, 2021

MiR-205-5p suppresses angiogenesis in gastric cancer by downregulating the expression of VEGFA and FGF1.

MiR-205-5p suppresses angiogenesis in gastric cancer by downregulating the expression of VEGFA and FGF1.

Journal: Experimental cell research

Published: November 07, 2020

Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin.

Skin damage in a patient with lipid storage myopathy with a novel ETFDH mutation responsive to riboflavin.

Journal: The International journal of neuroscience

Published: February 18, 2020

Observation of novel COX20 mutations related to autosomal recessive axonal neuropathy and static encephalopathy.

Observation of novel COX20 mutations related to autosomal recessive axonal neuropathy and static encephalopathy.

Journal: Human genetics

Published: February 21, 2019

Factors affecting the therapeutic effect of botulinum toxin A on trigeminal neuralgia: A follow-up retrospective study of 152 patients.

Factors affecting the therapeutic effect of botulinum toxin A on trigeminal neuralgia: A follow-up retrospective study of 152 patients.

Journal: Experimental and therapeutic medicine

Published: July 31, 2018

Harpagoside Rescues the Memory Impairments in Chronic Cerebral Hypoperfusion Rats by Inhibiting PTEN Activity.

Harpagoside Rescues the Memory Impairments in Chronic Cerebral Hypoperfusion Rats by Inhibiting PTEN Activity.

Journal: Journal of Alzheimer's disease : JAD

Published: April 05, 2018

Weird Laughing in Hyperekplexia: A new phenotype associated with a novel mutation in the GLRA1 gene?

Weird Laughing in Hyperekplexia: A new phenotype associated with a novel mutation in the GLRA1 gene?

Journal: Seizure

Published: November 11, 2017

Novel compound heterozygous mutations causing Kufs disease type B.

Novel compound heterozygous mutations causing Kufs disease type B.

Journal: The International journal of neuroscience

Published: November 10, 2017

A novel ETFDH mutation in an adult patient with late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

A novel ETFDH mutation in an adult patient with late-onset riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency.

Journal: The International journal of neuroscience

Published: September 16, 2017

Showing 1-12 of 16

Last Updated: 09/26/2026