Xiao G. Li

Hua Yuan North Road 49
Haidian, 100191, China

Last Updated: 09/26/2026

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Found 8 publications

Diagnostic Outcomes and Safety of CT-guided Synchronous Cryobiopsy and Microwave Ablation for High-risk Subsolid Nodules.

Diagnostic Outcomes and Safety of CT-guided Synchronous Cryobiopsy and Microwave Ablation for High-risk Subsolid Nodules.

Journal: Academic radiology

Published: August 19, 2025

Mutation screening of NEK1 in Chinese ALS patients.

Mutation screening of NEK1 in Chinese ALS patients.

Journal: Neurobiology of aging

Published: October 18, 2017

Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

Screening of the TBK1 gene in familial and sporadic amyotrophic lateral sclerosis patients of Chinese origin.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: June 05, 2016

Anti-inflammatory activities of fenoterol through β-arrestin-2 and inhibition of AMPK and NF-κB activation in AICAR-induced THP-1 cells.

Anti-inflammatory activities of fenoterol through β-arrestin-2 and inhibition of AMPK and NF-κB activation in AICAR-induced THP-1 cells.

Journal: Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie

Published: June 02, 2016

CHCHD10 is not a frequent causative gene in Chinese ALS patients.

CHCHD10 is not a frequent causative gene in Chinese ALS patients.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: April 15, 2016

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Identification of a novel loss-of-function C9orf72 splice site mutation in a patient with amyotrophic lateral sclerosis.

Journal: Neurobiology of aging

Published: March 05, 2016

Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.

Mutation spectrum of Chinese patients with familial and sporadic amyotrophic lateral sclerosis.

Journal: Journal of neurology, neurosurgery, and psychiatry

Published: February 15, 2016

Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS.

Whole-exome sequencing identifies a missense mutation in hnRNPA1 in a family with flail arm ALS.

Journal: Neurology

Published: February 06, 2016

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Last Updated: 09/26/2026