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Penicillamine increases free copper and enhances oxidative stress in the brain of toxic milk mice

PloS one, 2012-05, Vol.7 (5), p.e37709

2012

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Mesenchymal stem cell-derived exosomes improve motor function and attenuate neuropathology in a mouse model of Machado-Joseph disease

Stem cell research & therapy, 2020-06, Vol.11 (1), p.1-222, Article 222

2020

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A study of susceptibility-weighted imaging in patients with Wilson disease during the treatment of metal chelator

Journal of neurology, 2020-06, Vol.267 (6), p.1643-1650

2020

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Structural, Electronic, and Physical Properties of a New Layered Cr-Based Oxyarsenide Sr2Cr2AsO3

Materials, 2022-01, Vol.15 (3), p.802

2022

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Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression

CNS neuroscience & therapeutics, 2017-04, Vol.23 (4), p.321-328

2017

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Injury factors and pathological features of toxic milk mice during different disease stages

Brain and behavior, 2019-12, Vol.9 (12), p.e01459-n/a

2019

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The asymmetry of neural symptoms in Wilson's disease patients detecting by diffusion tensor imaging, resting‐state functional MRI, and susceptibility‐weighted imaging

Brain and behavior, 2018-05, Vol.8 (5), p.e00930-n/a

2018

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Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias

Brain (London, England : 1878), 2011-12, Vol.134 (12), p.3490-3498

2011

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Observation on the changes of clinical symptoms, blood and brain copper deposition in Wilson disease patients treated with dimercaptosuccinic acid for 2 years

Journal of clinical neuroscience, 2020-11, Vol.81, p.448-454

2020

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Superconductivity in kagome metal ThRu3Si2

Chinese physics B, 2024-05, Vol.33 (5)

2024

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Effects of tetrathiomolybdate and penicillamine on brain hydroxyl radical and free copper levels: A microdialysis study in vivo

Biochemical and biophysical research communications, 2015-02, Vol.458 (1), p.82-85

2015

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Diffusion tensor imaging of the extracorticospinal network in the brains of patients with Wilson disease

Journal of the neurological sciences, 2016-03, Vol.362, p.292-298

2016

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A novel mutation and functional implications of 5 variants in the PRRT2 gene in 20 paroxysmal kinesigenic dyskinesia pedigrees

Parkinsonism & related disorders, 2013-06, Vol.19 (6), p.639-642

2013

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Comparison of muscle pathology in riboflavin-responsive lipid storage myopathy before and after treatment: one case report and review of literature

Zhongguo xian dai shen jing ji bing za zhi, 2014, Vol.14 (6), p.485-489

2014

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Correction: Penicillamine Increases Free Copper and Enhances Oxidative Stress in the Brain of Toxic Milk Mice

PloS one, 2012-08, Vol.7 (8)

2012

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Peroxisomal acyl⁃CoA oxidase deficiency: one case report and literature review

Zhongguo xian dai shen jing ji bing za zhi, 2021-04, Vol.21 (4), p.281-288

2021

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A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family

Chinese medical journal, 2007-05, Vol.120 (9), p.834-837

2007

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Characterizing brain mineral deposition in patients with Wilson disease using susceptibility-weighted imaging

Neurology India, 2014-07, Vol.62 (4), p.362-366

2014

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Values of serum copper and serum free copper in the diagnosis and monitoring of Wilson's disease and its carriers

Zhong hua yi xue za zhi, 2011-10, Vol.91 (39), p.2757-2760

2011

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Clinical, pathological and genetic study of a kindred of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes

Chinese medical journal, 2005-04, Vol.118 (8), p.695-698

2005

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Recent advances of genetic research on paroxysmal kinesigenic dyskinesias

Zhonghua yi xue yi chuan xue za zhi, 2008-08, Vol.25 (4), p.410

2008

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Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias

Zhonghua yi xue yi chuan xue za zhi, 2005-02, Vol.22 (1), p.71

2005

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Structural, Electronic, and Physical Properties of a New Layered Cr-Based Oxyarsenide Sr 2 Cr 2 AsO 3

Materials, 2022-01, Vol.15 (3)

2022

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The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

Movement disorders, 2020-08, Vol.35 (8), p.1428-1437

2020

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Penicillamine increases free copper and enhances oxidative stress in the brain of toxic milk mice

Mesenchymal stem cell-derived exosomes improve motor function and attenuate neuropathology in a mouse model of Machado-Joseph disease

A study of susceptibility-weighted imaging in patients with Wilson disease during the treatment of metal chelator

Structural, Electronic, and Physical Properties of a New Layered Cr-Based Oxyarsenide Sr2Cr2AsO3

Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression

Injury factors and pathological features of toxic milk mice during different disease stages

The asymmetry of neural symptoms in Wilson's disease patients detecting by diffusion tensor imaging, resting‐state functional MRI, and susceptibility‐weighted imaging

Identification of PRRT2 as the causative gene of paroxysmal kinesigenic dyskinesias

Observation on the changes of clinical symptoms, blood and brain copper deposition in Wilson disease patients treated with dimercaptosuccinic acid for 2 years

Superconductivity in kagome metal ThRu3Si2

Effects of tetrathiomolybdate and penicillamine on brain hydroxyl radical and free copper levels: A microdialysis study in vivo

Diffusion tensor imaging of the extracorticospinal network in the brains of patients with Wilson disease

A novel mutation and functional implications of 5 variants in the PRRT2 gene in 20 paroxysmal kinesigenic dyskinesia pedigrees

Comparison of muscle pathology in riboflavin-responsive lipid storage myopathy before and after treatment: one case report and review of literature

Correction: Penicillamine Increases Free Copper and Enhances Oxidative Stress in the Brain of Toxic Milk Mice

Peroxisomal acyl⁃CoA oxidase deficiency: one case report and literature review

A SPG3A mutation with a novel foot phenotype of hereditary spastic paraplegia in a Chinese Han family

Characterizing brain mineral deposition in patients with Wilson disease using susceptibility-weighted imaging

Values of serum copper and serum free copper in the diagnosis and monitoring of Wilson's disease and its carriers

Clinical, pathological and genetic study of a kindred of mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes

Recent advances of genetic research on paroxysmal kinesigenic dyskinesias

Molecular genetics and its clinical application in the diagnosis of spinocerebellar ataxias

Structural, Electronic, and Physical Properties of a New Layered Cr-Based Oxyarsenide Sr 2 Cr 2 AsO 3

TMEM151A Variants Cause Paroxysmal Kinesigenic Dyskinesia: A Large‐Sample Study

The Phenotypic and Genetic Spectrum of Paroxysmal Kinesigenic Dyskinesia in China

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