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Factors affecting doctor’s recommendation for mobile health services

Digital health, 2022, Vol.8, p.205520762211259-20552076221125976

2022

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Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

Frontiers in immunology, 2021-11, Vol.12, p.761354-761354

2021

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CASPR2 antibody associated neurological syndromes in children

Scientific reports, 2023-02, Vol.13 (1), p.2073-2073, Article 2073

2023

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Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review

Zhonghua yi xue yi chuan xue za zhi, 2023-04, Vol.40 (4), p.385

2023

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A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy

Neurological sciences, 2021, Vol.42 (1), p.329-331

2021

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Compound heterozygous mutations in PUS3 gene identified in a Chinese infant with severe epileptic encephalopathy and multiple malformations

Neurological sciences, 2020-02, Vol.41 (2), p.465-467

2020

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Video-electroencephalographic findings and clinical characteristics of bathing seizures in children

Frontiers in neurology, 2024-02, Vol.15, p.1366206-1366206

2024

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Effective treatments for FGF12-related early-onset epileptic encephalopathies patients

Brain & development (Tokyo. 1979), 2021-09, Vol.43 (8), p.851-856

2021

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Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

Frontiers in immunology, 2023-04, Vol.14, p.1140872-1140872

2023

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Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

Frontiers in neuroscience, 2023-05, Vol.17, p.1106214-1106214

2023

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Facing the impact of the COVID-19 pandemic: How can we allocate outpatient doctor resources more effectively?

Tropical medicine and infectious disease, 2022-08, Vol.7 (8), p.1-11

2022

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Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene

Zhonghua yi xue yi chuan xue za zhi, 2023-04, Vol.40 (4), p.413

2023

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Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations

Frontiers in neuroscience, 2022-12, Vol.16, p.1076183-1076183

2022

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Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients

Frontiers in neurology, 2023-12, Vol.14, p.1310419-1310419

2023

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Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study

Frontiers in pediatrics, 2022-07, Vol.10, p.880693-880693

2022

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Nabais Sa‐de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report

Molecular genetics & genomic medicine, 2022-12, Vol.10 (12), p.e2075-n/a

2022

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Enhanced photocatalytic activity and mechanism of Ti3C2−OH/Bi2WO6:Yb3+, Tm3+ towards degradation of RhB under visible and near infrared light irradiation

Materials research bulletin, 2020-01, Vol.121, p.110618, Article 110618

2020

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Selective Hydrogenation of Polyenes in Biomass-Derived Cardanol over the Trimetallic Ni–Co–Cu Catalyst Supported on Morphologically Controlled Alumina

Industrial & engineering chemistry research, 2023-11, Vol.62 (43), p.17440-17450

2023

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Enhanced visible light photocatalytic activity of CdS with alkalized Ti3C2 nano-sheets as co-catalyst for degradation of rhodamine B

Journal of materials science. Materials in electronics, 2019-08, Vol.30 (16), p.14954-14966

2019

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Facile preparation of Yb3+/Tm3+ co-doped Ti3C2/Ag/Ag3VO4 composite with an efficient charge separation for boosting visible-light photocatalytic activity

Applied surface science, 2020-10, Vol.527, p.146909, Article 146909

2020

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S-scheme heterojunction g-C3N4/Ag/AgNCO for efficient tetracycline removal in a photo-assisted peroxymonosulfate system

Separation and purification technology, 2022-09, Vol.296, p.121210, Article 121210

2022

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Synergistic removal of organic pollutants by Co-doped MIL-53(Al) composite through the integrated adsorption/photocatalysis

Journal of solid state chemistry, 2022-12, Vol.316, p.123582, Article 123582

2022

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Durable and efficient urea electrosynthesis using carbon dioxide and nitrate over defect-rich In 2 O 3 nanotubes

Green chemistry : an international journal and green chemistry resource : GC, 2024-06, Vol.26 (11), p.6812-6821

2024

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Durable and efficient urea electrosynthesis using carbon dioxide and nitrate over defect-rich InO nanotubes

Green chemistry : an international journal and green chemistry resource : GC, 2024-06, Vol.26 (11), p.6812-6821

2024

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Highly efficient and selective electrosynthesis of urea via co-reduction of carbon dioxide and nitrate over the TiN catalyst

Chemical engineering journal (Lausanne, Switzerland : 1996), 2024-04, Vol.486, p.150178, Article 150178

2024

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Factors affecting doctor’s recommendation for mobile health services

Autoimmune Glial Fibrillary Acidic Protein Astrocytopathy in Children: A Retrospective Analysis of 35 Cases

CASPR2 antibody associated neurological syndromes in children

Genetic analysis of a child with early onset neurodevelopmental disorder with involuntary movement and a literature review

A de novo mutation in SMC1A gene identified in a Chinese infant with nonclassical Cornelia de Lange syndrome and drug-resistant epilepsy

Compound heterozygous mutations in PUS3 gene identified in a Chinese infant with severe epileptic encephalopathy and multiple malformations

Video-electroencephalographic findings and clinical characteristics of bathing seizures in children

Effective treatments for FGF12-related early-onset epileptic encephalopathies patients

Clinical analysis of 173 pediatric patients with antibody-mediated autoimmune diseases of the central nervous system: a single-center cohort study

Clinical spectrum of contactin-associated protein 2 autoimmune encephalitis in children

Facing the impact of the COVID-19 pandemic: How can we allocate outpatient doctor resources more effectively?

Analysis of clinical phenotype and genetic variants in a child with mitochondrial F-S disease due to variants of FDXR gene

Clinical and genetic analyses of premature mitochondrial encephalopathy with epilepsia partialis continua caused by novel biallelic NARS2 mutations

Clinical characteristics and genetic analysis of pediatric patients with sodium channel gene mutation-related childhood epilepsy: a review of 94 patients

Clinical Characteristics and Short-Term Prognosis of Children With Antibody-Mediated Autoimmune Encephalitis: A Single-Center Cohort Study

Nabais Sa‐de Vries syndrome in a Chinese infant associated with a novel SPOP mutation: A clinical study and genetic report

Enhanced photocatalytic activity and mechanism of Ti3C2−OH/Bi2WO6:Yb3+, Tm3+ towards degradation of RhB under visible and near infrared light irradiation

Selective Hydrogenation of Polyenes in Biomass-Derived Cardanol over the Trimetallic Ni–Co–Cu Catalyst Supported on Morphologically Controlled Alumina

Enhanced visible light photocatalytic activity of CdS with alkalized Ti3C2 nano-sheets as co-catalyst for degradation of rhodamine B

Facile preparation of Yb3+/Tm3+ co-doped Ti3C2/Ag/Ag3VO4 composite with an efficient charge separation for boosting visible-light photocatalytic activity

S-scheme heterojunction g-C3N4/Ag/AgNCO for efficient tetracycline removal in a photo-assisted peroxymonosulfate system

Synergistic removal of organic pollutants by Co-doped MIL-53(Al) composite through the integrated adsorption/photocatalysis

Durable and efficient urea electrosynthesis using carbon dioxide and nitrate over defect-rich In 2 O 3 nanotubes

Durable and efficient urea electrosynthesis using carbon dioxide and nitrate over defect-rich InO nanotubes

Highly efficient and selective electrosynthesis of urea via co-reduction of carbon dioxide and nitrate over the TiN catalyst

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