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Body mass index and remote ischaemic conditioning efficacy in acute ischaemic stroke patients: A post hoc analysis of the Remote Ischaemic Conditioning for Acute Moderate Ischaemic Stroke (RICAMIS) trial

Diabetes, obesity & metabolism, 2024-07, Vol.26 (7), p.2993-2996

2024

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Efficacy of remote ischemic conditioning does not differ between men and women: A secondary analysis of the RICAMIS study

European journal of neurology, 2023-07, Vol.30 (7), p.2022-2030

2023

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Central pontine myelinolysis: a rare finding in hyperosmolar hyperglycemia

Frontiers in neurology, 2023-10, Vol.14

2023

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Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease

Bioscience reports, 2021-06, Vol.41 (6)

2021

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Prevalent characteristics of human papillomavirus infection in 29,508 women in Jinshan District, Shanghai

Taiwanese journal of obstetrics & gynecology, 2022-11, Vol.61 (6), p.971-976

2022

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Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families

International journal of ophthalmology, 2022-12, Vol.15 (12), p.1915-1923

2022

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Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients

Stem cell research & therapy, 2017-09, Vol.8 (1), p.209-209, Article 209

2017

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Excimer Laser Phototherapeutic Keratectomy for the Treatment of Clinically Presumed Fungal Keratitis

Journal of Ophthalmology, 2014-01, Vol.2014 (4), p.243-250

2014

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Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

Bioscience reports, 2020-01, Vol.40 (1)

2020

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Detection of Novel BEST1 Variations in Autosomal Recessive Bestrophinopathy Using Third-generation Sequencing

Current medical science, 2024-04, Vol.44 (2), p.419-425

2024

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Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

Bioscience reports, 2016-02, Vol.36 (1), p.e00289-e00289

2016

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Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology

Molecular genetics and genomics : MGG, 2015-02, Vol.290 (1), p.353-363

2015

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Haplotype analysis of association of the MYOC gene with primary angle-closure glaucoma in a Han Chinese population

Genetic testing and molecular biomarkers, 2015-01, Vol.19 (1), p.3-8

2015

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A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Lipids in health and disease, 2014-05, Vol.13 (1), p.75-75, Article 75

2014

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ZL006 mitigates anxiety-like behaviors induced by closed head injury through modulation of the neural circuit from the medial prefrontal cortex to amygdala

Cerebral cortex (New York, N.Y. 1991), 2024-06, Vol.34 (6)

2024

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Sex Differences in the Dual Antiplatelet Therapy Versus Alteplase for Patients with Minor Nondisabling Acute Ischemic Stroke: A Secondary Analysis of the ARAMIS Study

CNS drugs, 2024-08, Vol.38 (8), p.649-659

2024

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Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology

Molecular vision, 2014-04, Vol.20, p.553-560

2014

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Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families

Current medical science, 2024-08, Vol.44 (4), p.820-826

2024

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Erratum to: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Lipids in health and disease, 2014-07, Vol.13 (1), Article 110

2014

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Correction: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Lipids in health and disease, 2014-07, Vol.13 (1), p.110-110

2014

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Central pontine myelinolysis: a rare finding in hyperosmolar hyperglycemia

Frontiers in neurology, 2023, Vol.14, p.1216328-1216328

2023

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A new method for position-sensitive measurement of beta surface contamination

Nuclear science and techniques, 2017-02, Vol.28 (2), p.49-56, Article 23

2017

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Comparison of MRI and CT‐Based Radiomics and Their Combination for Early Identification of Pathological Response to Neoadjuvant Chemotherapy in Locally Advanced Gastric Cancer

Journal of magnetic resonance imaging, 2023-09, Vol.58 (3), p.907-923

2023

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Optimal timing for carbon capture retrofitting in biomass-coal combined heat and power plants in China

Journal of cleaner production, 2021-04, Vol.293, p.126134, Article 126134

2021

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Biochanin A Alleviates Cerebral Ischemia/Reperfusion Injury by Suppressing Endoplasmic Reticulum Stress-Induced Apoptosis and p38MAPK Signaling Pathway In Vivo and In Vitro

Frontiers in endocrinology (Lausanne), 2021-07, Vol.12, p.646720-646720

2021

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Body mass index and remote ischaemic conditioning efficacy in acute ischaemic stroke patients: A post hoc analysis of the Remote Ischaemic Conditioning for Acute Moderate Ischaemic Stroke (RICAMIS) trial

Efficacy of remote ischemic conditioning does not differ between men and women: A secondary analysis of the RICAMIS study

Central pontine myelinolysis: a rare finding in hyperosmolar hyperglycemia

Targeted next-generation sequencing identifies ABCA4 mutations in Chinese families with childhood-onset and adult-onset Stargardt disease

Prevalent characteristics of human papillomavirus infection in 29,508 women in Jinshan District, Shanghai

Various phenotypes of autosomal dominant cone-rod dystrophy with cone-rod homeobox mutation in two Chinese families

Long-term safety of human retinal progenitor cell transplantation in retinitis pigmentosa patients

Excimer Laser Phototherapeutic Keratectomy for the Treatment of Clinically Presumed Fungal Keratitis

Identification of 13 novel USH2A mutations in Chinese retinitis pigmentosa and Usher syndrome patients by targeted next-generation sequencing

Detection of Novel BEST1 Variations in Autosomal Recessive Bestrophinopathy Using Third-generation Sequencing

Novel compound heterozygous mutation in the CNGA1 gene underlie autosomal recessive retinitis pigmentosa in a Chinese family

Detecting novel genetic mutations in Chinese Usher syndrome families using next-generation sequencing technology

Haplotype analysis of association of the MYOC gene with primary angle-closure glaucoma in a Han Chinese population

A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

ZL006 mitigates anxiety-like behaviors induced by closed head injury through modulation of the neural circuit from the medial prefrontal cortex to amygdala

Sex Differences in the Dual Antiplatelet Therapy Versus Alteplase for Patients with Minor Nondisabling Acute Ischemic Stroke: A Secondary Analysis of the ARAMIS Study

Detecting genetic variations in hereditary retinal dystrophies with next-generation sequencing technology

Analysis of Phenotypes Associated with Deficiency of PAX6 Haplotypes in Chinese Aniridia Families

Erratum to: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Correction: A novel mutation in C5L2 gene was associated with hyperlipidemia and retinitis pigmentosa in a Chinese family

Central pontine myelinolysis: a rare finding in hyperosmolar hyperglycemia

A new method for position-sensitive measurement of beta surface contamination

Comparison of MRI and CT‐Based Radiomics and Their Combination for Early Identification of Pathological Response to Neoadjuvant Chemotherapy in Locally Advanced Gastric Cancer

Optimal timing for carbon capture retrofitting in biomass-coal combined heat and power plants in China

Biochanin A Alleviates Cerebral Ischemia/Reperfusion Injury by Suppressing Endoplasmic Reticulum Stress-Induced Apoptosis and p38MAPK Signaling Pathway In Vivo and In Vitro

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