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Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation

Neurological sciences, 2021-12, Vol.42 (12), p.5123-5130

2021

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A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt‐ND variants

Annals of clinical and translational neurology, 2023-06, Vol.10 (6), p.1035-1045

2023

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Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNAGln m.4349C>T Variant

Annals of clinical and translational neurology, 2020-06, Vol.7 (6), p.980-991

2020

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C-reactive protein for predicting all-cause mortality in patients with acute ischemic stroke: a meta-analysis

Bioscience reports, 2019-02, Vol.39 (2)

2019

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Reversible cerebral artery constriction accompanied with stroke-like episode in MELAS: A case series

Journal of the neurological sciences, 2022-10, Vol.441, p.120345-120345, Article 120345

2022

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MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNATrp and remarkable mitochondrial dysfunction

Journal of medical genetics, 2022-01, Vol.59 (1), p.79-87

2022

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MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNA Trp and remarkable mitochondrial dysfunction

Journal of medical genetics, 2022-01, Vol.59 (1), p.79-87

2022

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Bezafibrate Rescues Mitochondrial Encephalopathy in Mice via Induction of Daily Torpor and Hypometabolic State

Neurotherapeutics, 2022-04, Vol.19 (3), p.994-1006

2022

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A novel nonsense variant in MT-CO3 causes MELAS syndrome

Neuromuscular disorders : NMD, 2021-06, Vol.31 (6), p.558-565

2021

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Leber’s hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation

Neurological sciences, 2022-09, Vol.43 (9), p.5581-5592

2022

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Mitochondrial myopathy without extraocular muscle involvement: a unique clinicopathologic profile

Journal of neurology, 2024-02, Vol.271 (2), p.864-876

2024

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ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A Dehydrogenation Deficiency

Annals of neurology, 2018-11, Vol.84 (5), p.659-673

2018

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A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome

Mitochondrion, 2020-09, Vol.54, p.57-64

2020

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A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function

Mitochondrion, 2021-03, Vol.57, p.1-8

2021

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A mitochondrial myopathy-associated tRNA Ser(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function

Mitochondrion, 2021-03, Vol.57, p.1

2021

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Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNA Gln m.4349C>T Variant

Annals of clinical and translational neurology, 2020-06, Vol.7 (6), p.980-991

2020

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Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

Chinese medical journal, 2019-03, Vol.132 (6), p.716-718

2019

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A Dynamic Keyboard with Hierarchical Mathematical Symbols for Multi-Subject e-Learning Systems

2022 International Conference on Intelligent Education and Intelligent Research (IEIR), 2022, p.156-161

2022

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An Intelligent Tutoring System for Math Word Problem Solving with Tutorial Solution Generation

2022 International Conference on Intelligent Education and Intelligent Research (IEIR), 2022, p.183-188

2022

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A Novel m.4349c>T Mutation Causes Mitochondrial Encephalopathy by Disturbing Translation Machinery and Mitochondrial Function

SSRN Electronic Journal

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Quantitative analysis of internal components of the human crystalline lens during accommodation in adults

Scientific reports, 2021-03, Vol.11 (1), p.6688-6688, Article 6688

2021

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A novel technology for in vivo detection of cell type-specific neural connection with AQP1-encoding rAAV2-retro vector and metal-free MRI

NeuroImage (Orlando, Fla.), 2022-09, Vol.258, p.119402-119402, Article 119402

2022

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Sufentanil EC50 for endotracheal intubation with aerosol inhalation of carbonated lidocaine by ultrasonic atomizer

BMC anesthesiology, 2021-05, Vol.21 (1), p.144-144, Article 144

2021

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Investigation of metabolic kinetics in different brain regions of awake rats using the [1H-13C]-NMR technique

Journal of pharmaceutical and biomedical analysis, 2021-09, Vol.204, p.114240-114240, Article 114240

2021

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Endoplasmic Reticulum Stress in Spinal Cord Contributes to the Development of Morphine Tolerance

Frontiers in molecular neuroscience, 2018-03, Vol.11, p.72-72

2018

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Leber hereditary optic neuropathy and dystonia overlapping mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes due to m.14459G>A mutation

A different pattern of clinical, muscle pathology and brain MRI findings in MELAS with mt‐ND variants

Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNAGln m.4349C>T Variant

C-reactive protein for predicting all-cause mortality in patients with acute ischemic stroke: a meta-analysis

Reversible cerebral artery constriction accompanied with stroke-like episode in MELAS: A case series

MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNATrp and remarkable mitochondrial dysfunction

MELAS-associated m.5541C>T mutation caused instability of mitochondrial tRNA Trp and remarkable mitochondrial dysfunction

Bezafibrate Rescues Mitochondrial Encephalopathy in Mice via Induction of Daily Torpor and Hypometabolic State

A novel nonsense variant in MT-CO3 causes MELAS syndrome

Leber’s hereditary optic neuropathy plus dystonia caused by the mitochondrial ND1 gene m.4160 T > C mutation

Mitochondrial myopathy without extraocular muscle involvement: a unique clinicopathologic profile

ETFDH Mutations and Flavin Adenine Dinucleotide Homeostasis Disturbance Are Essential for Developing Riboflavin‐Responsive Multiple Acyl–Coenzyme A Dehydrogenation Deficiency

A novel m.11406 T > A mutation in mitochondrial ND4 gene causes MELAS syndrome

A mitochondrial myopathy-associated tRNASer(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function

A mitochondrial myopathy-associated tRNA Ser(UCN) 7453G>A mutation alters tRNA metabolism and mitochondrial function

Mitochondrial encephalopathy Due to a Novel Pathogenic Mitochondrial tRNA Gln m.4349C>T Variant

Late-onset mitochondrial disease in a patient with MELAS and mitochondrial DNA T14487C mutation

A Dynamic Keyboard with Hierarchical Mathematical Symbols for Multi-Subject e-Learning Systems

An Intelligent Tutoring System for Math Word Problem Solving with Tutorial Solution Generation

A Novel m.4349c>T Mutation Causes Mitochondrial Encephalopathy by Disturbing Translation Machinery and Mitochondrial Function

Quantitative analysis of internal components of the human crystalline lens during accommodation in adults

A novel technology for in vivo detection of cell type-specific neural connection with AQP1-encoding rAAV2-retro vector and metal-free MRI

Sufentanil EC50 for endotracheal intubation with aerosol inhalation of carbonated lidocaine by ultrasonic atomizer

Investigation of metabolic kinetics in different brain regions of awake rats using the [1H-13C]-NMR technique

Endoplasmic Reticulum Stress in Spinal Cord Contributes to the Development of Morphine Tolerance

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