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Assessing the effects of ROO and tariff margin on China-ASEAN free trade agreement utilization

PloS one, 2023-05, Vol.18 (5), p.e0286106-e0286106

2023

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Genotype–phenotype characteristics and baseline natural history of Chinese myelin protein zero gene related neuropathy patients

European journal of neurology, 2023-04, Vol.30 (4), p.1069-1079

2023

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Listeria Monocytogenes Meningoencephalitis Due to IRAK4 Deficiency

Journal of clinical immunology, 2021-10, Vol.41 (7), p.1677-1680

2021

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Transfer of miR-877–3p via extracellular vesicles derived from dental pulp stem cells attenuates neuronal apoptosis and facilitates early neurological functional recovery after cerebral ischemia–reperfusion injury through the Bclaf1/P53 signaling pathway

Pharmacological research, 2024-08, Vol.206, p.107266, Article 107266

2024

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The Protective Effect of Vitexin Compound B-1 on Rat Cerebral I/R Injury through a Mechanism Involving Modulation of miR-92b/NOX4 Pathway

CNS & neurological disorders drug targets, 2023, Vol.22 (1), p.137-147

2023

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Clinical and genetic features of Charcot-Marie-Tooth disease patients with IGHMBP2 mutations

Neuromuscular disorders : NMD, 2022-07, Vol.32 (7), p.564-571

2022

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Mutation spectrum of amyotrophic lateral sclerosis in Central South China

Neurobiology of aging, 2021-11, Vol.107, p.181-188

2021

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Intermediate Charcot-Marie-Tooth disease

Neuroscience bulletin, 2014-12, Vol.30 (6), p.999-1009

2014

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A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family

Clinical genetics, 2019-08, Vol.96 (2), p.176-182

2019

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Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections

Microbiology spectrum, 2024-01, Vol.12 (1), p.e0226423-e0226423

2024

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Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis

Frontiers in neurology, 2021-06, Vol.12, p.628710-628710

2021

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One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families

Frontiers in neurology, 2022-01, Vol.12, p.736704-736704

2022

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Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families

Frontiers in neurology, 2020-12, Vol.11, p.603003-603003

2020

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Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China

Translational neurodegeneration, 2021-02, Vol.10 (1), p.7-7, Article 7

2021

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The Impact of U.S. Trade Policy Uncertainty on the Trade Margins of China’s Export to the U.S

Sustainability, 2022-11, Vol.14 (22), p.15101

2022

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MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patients

Journal of the peripheral nervous system, 2016-03, Vol.21 (1), p.38-44

2016

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Improved Device Lifetime In Organic Light Emitting Devices By Using a Solution-Processed Mixing Single Layer Structure

Journal of Photopolymer Science and Technology, 2015/05/11, Vol.28(4), pp.595-599

2015

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Association between weekend catch-up sleep and depression of the United States population from 2017 to 2018: A cross-sectional study

Sleep medicine, 2024-07, Vol.119, p.9-16

2024

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Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot–Marie–Tooth Disease

Journal of neurology, 2024, Vol.271 (1), p.497-503

2024

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A novel transgenic mouse model of Chinese Charcot-Marie-Tooth disease type 2L

Neural regeneration research, 2014-02, Vol.9 (4), p.413-419

2014

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SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS

Biochimica et biophysica acta. Molecular and cell biology of lipids, 2023-09, Vol.1868 (9), p.159359-159359, Article 159359

2023

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A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy

Neurology, 2015-06, Vol.84 (24), p.2430-2437

2015

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Nature genetics, 2020-05, Vol.52 (5), p.473-481

2020

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Genotype–phenotype correlations of AR‐CMT2S in a cohort of axonal Charcot–Marie–Tooth patients from Central South China

Journal of the peripheral nervous system, 2024-06, Vol.29 (2), p.243-251

2024

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The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies

Journal of neurology, 2023-10, Vol.270 (10), p.4959-4967

2023

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Assessing the effects of ROO and tariff margin on China-ASEAN free trade agreement utilization

Genotype–phenotype characteristics and baseline natural history of Chinese myelin protein zero gene related neuropathy patients

Listeria Monocytogenes Meningoencephalitis Due to IRAK4 Deficiency

Transfer of miR-877–3p via extracellular vesicles derived from dental pulp stem cells attenuates neuronal apoptosis and facilitates early neurological functional recovery after cerebral ischemia–reperfusion injury through the Bclaf1/P53 signaling pathway

The Protective Effect of Vitexin Compound B-1 on Rat Cerebral I/R Injury through a Mechanism Involving Modulation of miR-92b/NOX4 Pathway

Clinical and genetic features of Charcot-Marie-Tooth disease patients with IGHMBP2 mutations

Mutation spectrum of amyotrophic lateral sclerosis in Central South China

Intermediate Charcot-Marie-Tooth disease

A novel WARS mutation (p.Asp314Gly) identified in a Chinese distal hereditary motor neuropathy family

Metagenomic next-generation sequencing of cell-free DNA for the identification of viruses causing central nervous system infections

Evaluation of Peripheral Immune Activation in Amyotrophic Lateral Sclerosis

One PMP22/MPZ and Three MFN2/GDAP1 Concomitant Variants Occurred in a Cohort of 189 Chinese Charcot-Marie-Tooth Families

Genetic and Clinical Features in 24 Chinese Distal Hereditary Motor Neuropathy Families

Recommendations for the diagnosis and treatment of paroxysmal kinesigenic dyskinesia: an expert consensus in China

The Impact of U.S. Trade Policy Uncertainty on the Trade Margins of China’s Export to the U.S

MFN2-related genetic and clinical features in a cohort of Chinese CMT2 patients

Improved Device Lifetime In Organic Light Emitting Devices By Using a Solution-Processed Mixing Single Layer Structure

Association between weekend catch-up sleep and depression of the United States population from 2017 to 2018: A cross-sectional study

Phenotype-driven reanalysis reveals five novel pathogenic variants in 40 exome-negative families with Charcot–Marie–Tooth Disease

A novel transgenic mouse model of Chinese Charcot-Marie-Tooth disease type 2L

SPTLC1 p.Leu38Arg, a novel mutation associated with childhood ALS

A SIGMAR1 splice-site mutation causes distal hereditary motor neuropathy

Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes

Genotype–phenotype correlations of AR‐CMT2S in a cohort of axonal Charcot–Marie–Tooth patients from Central South China

The genetic and clinical spectrum in a cohort of 39 families with complex inherited peripheral neuropathies

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