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Understanding of variant selection and twin patterns in compressed Mg alloy sheets via combined analysis of Schmid factor and strain compatibility factor

Materials science & engineering. A, Structural materials : properties, microstructure and processing, 2014-07, Vol.609, p.92-101

2014

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Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and Toddlers

Pediatric neurology, 2021-06, Vol.119, p.27-33

2021

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A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiency

Brain & development (Tokyo. 1979), 2019-02, Vol.41 (2), p.205-209

2019

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Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital

Annals of neurology, 2022-04, Vol.91 (4), p.466-482

2022

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Neurophenotype and genetic analysis of children with Aicardi‐Goutières syndrome in China

Pediatric investigation, 2024-09, Vol.8 (3), p.193-200

2024

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Bilateral globus pallidus internus‐deep brain stimulation in a 5‐year‐old boy with SGCE‐related myoclonus dystonia syndrome

Pediatric investigation, 2024-06, Vol.8 (2), p.154-156

2024

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Influence of observation plane on twin variant identification in magnesium via trace and misorientation analysis

Materials science & engineering. A, Structural materials : properties, microstructure and processing, 2014-11, Vol.618, p.558-562

2014

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Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case report

Frontiers in neurology, 2022-09, Vol.13

2022

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Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A

Scientific reports, 2017-10, Vol.7 (1), p.13686-9, Article 13686

2017

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Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese Patients

Genes, 2022-05, Vol.13 (5), p.908

2022

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Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers’ Syndrome Genotypes

Frontiers in pharmacology, 2021-10, Vol.12, p.669516-669516

2021

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The clinical and genetic characteristics in children with mitochondrial disease in China

Science China. Life sciences, 2017-07, Vol.60 (7), p.746-757

2017

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Improvement of thermal stability of Ta-N film in Cu metallization by a Zr-Si interlayer

E3S Web of Conferences, 2021, Vol.271, p.4015

2021

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Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

Pediatric investigation, 2022-03, Vol.6 (1), p.5-10

2022

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Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients

Molecular genetics & genomic medicine, 2022-03, Vol.10 (3), p.e1825-n/a

2022

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Application of laser remote sensing technology and super continuous spectrum laser

E3S web of conferences, 2020-01, Vol.165, p.3002

2020

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Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea

Frontiers in pharmacology, 2019-03, Vol.10, p.259

2019

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Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

Acta epileptologica, 2020-09, Vol.2 (1), p.1-15, Article 14

2020

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An inherited KMT2B duplication variant in a Chinese family with dystonia and/or development delay

Parkinsonism & related disorders, 2019-06, Vol.63, p.227-228

2019

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Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Journal of human genetics, 2011-02, Vol.56 (2), p.138-142

2011

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Transcriptomic analysis reveals the mechanism of host growth promotion by endophytic fungus of Rumex gmelinii Turcz

Archives of microbiology, 2022-07, Vol.204 (7), p.443-443, Article 443

2022

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Multi-source deep transfer learning algorithm based on feature alignment

The Artificial intelligence review, 2023-10, Vol.56 (Suppl 1), p.769-791

2023

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Basal nuclei lesions and cholecystitis as initial findings of late infantile metachromatic leukodystrophy

Clinical neurology and neurosurgery, 2023-01, Vol.224, p.107543, Article 107543

2023

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Two Chinese siblings with two novel KCTD7 mutations have dystonia or seizures and epileptic discharge on electroencephalograms

Seizure (London, England), 2019-08, Vol.70, p.27-29

2019

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Crystallographic analysis on the activation of multiple twins in rolled AZ31 Mg alloy sheets during uniaxial and plane strain compression

Materials science & engineering. A, Structural materials : properties, microstructure and processing, 2016-01, Vol.652, p.42-50

2016

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Understanding of variant selection and twin patterns in compressed Mg alloy sheets via combined analysis of Schmid factor and strain compatibility factor

Clinical Features and Outcomes of Anti-N-Methyl-d-Aspartate Receptor Encephalitis in Infants and Toddlers

A novel DDC gene deletion mutation in two Chinese mainland siblings with aromatic l-amino acid decarboxylase deficiency

Leigh Syndrome: A Study of 209 Patients at the Beijing Children's Hospital

Neurophenotype and genetic analysis of children with Aicardi‐Goutières syndrome in China

Bilateral globus pallidus internus‐deep brain stimulation in a 5‐year‐old boy with SGCE‐related myoclonus dystonia syndrome

Influence of observation plane on twin variant identification in magnesium via trace and misorientation analysis

Oculogyric crisis mimicked epilepsy in a Chinese aromatic L-amino acid decarboxylase-deficiency patient: A case report

Molecular spectrum of excision repair cross-complementation group 8 gene defects in Chinese patients with Cockayne syndrome type A

Novel Loss-of-Function Variants in CHD2 Cause Childhood-Onset Epileptic Encephalopathy in Chinese Patients

Clinical Attributes and Electroencephalogram Analysis of Patients With Varying Alpers’ Syndrome Genotypes

The clinical and genetic characteristics in children with mitochondrial disease in China

Improvement of thermal stability of Ta-N film in Cu metallization by a Zr-Si interlayer

Chinese patients with p.Arg756 mutations of ATP1A3: Clinical manifestations, treatment, and follow‐up

Expanding the mutational spectrum of Rahman syndrome: A rare disorder with severe intellectual disability and particular facial features in two Chinese patients

Application of laser remote sensing technology and super continuous spectrum laser

Compound Heterozygous CHAT Gene Mutations of a Large Deletion and a Missense Variant in a Chinese Patient With Severe Congenital Myasthenic Syndrome With Episodic Apnea

Clinical phenotype features and genetic etiologies of 38 children with progressive myoclonic epilepsy

An inherited KMT2B duplication variant in a Chinese family with dystonia and/or development delay

Identification of novel MLC1 mutations in Chinese patients with megalencephalic leukoencephalopathy with subcortical cysts (MLC)

Transcriptomic analysis reveals the mechanism of host growth promotion by endophytic fungus of Rumex gmelinii Turcz

Multi-source deep transfer learning algorithm based on feature alignment

Basal nuclei lesions and cholecystitis as initial findings of late infantile metachromatic leukodystrophy

Two Chinese siblings with two novel KCTD7 mutations have dystonia or seizures and epileptic discharge on electroencephalograms

Crystallographic analysis on the activation of multiple twins in rolled AZ31 Mg alloy sheets during uniaxial and plane strain compression

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