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The Genetics of Primary Familial Brain Calcification: A Literature Review

International journal of molecular sciences, 2023-06, Vol.24 (13), p.10886

2023

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Blood neurofilament light chain as a surrogate marker for dystonia

European journal of neurology, 2023-10, Vol.30 (10), p.3098-3104

2023

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Miro1 improves the exogenous engraftment efficiency and therapeutic potential of mitochondria transfer using Wharton's jelly mesenchymal stem cells

Mitochondrion, 2024-05, Vol.76, p.101856-101856, Article 101856

2024

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Recessively‐Inherited Adult‐Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene

Movement disorders, 2020-09, Vol.35 (9), p.1662-1667

2020

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Iron Brain Menace: The Involvement of Ferroptosis in Parkinson Disease

Cells (Basel, Switzerland), 2022-11, Vol.11 (23), p.3829

2022

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Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial

Critical care (London, England), 2015-02, Vol.19 (1), p.49-49, Article 49

2015

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Higher prevalence of idiopathic normal pressure hydrocephalus‐like MRI features in progressive supranuclear palsy: An imaging reminder of atypical parkinsonism

Brain and behavior, 2023-02, Vol.13 (2), p.e2884-n/a

2023

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Mitochondrial dysfunctions in leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL)

PloS one, 2019-10, Vol.14 (10), p.e0224173-e0224173

2019

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Brain hypoperfusion and nigrostriatal dopaminergic dysfunction in primary familial brain calcification caused by novel MYORG variants: case report

BMC neurology, 2020-09, Vol.20 (1), p.329-329, Article 329

2020

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Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease

Cells (Basel, Switzerland), 2024-04, Vol.13 (8), p.694

2024

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Genetic analysis of IRF2BPL in a Taiwanese dystonia cohort: The genotype and phenotype correlation

Annals of clinical and translational neurology, 2024-06, Vol.11 (6), p.1557-1566

2024

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Glucagon-Like Peptide-1 Receptor Agonist Ameliorates 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine (MPTP) Neurotoxicity Through Enhancing Mitophagy Flux and Reducing α-Synuclein and Oxidative Stress

Frontiers in molecular neuroscience, 2021-07, Vol.14, p.697440-697440

2021

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Level and Value of Circulating Endothelial Progenitor Cells in Patients After Acute Ischemic Stroke

Stroke (1970), 2008, Vol.39 (1), p.69-74

2008

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Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review

BMC neurology, 2017-10, Vol.17 (1), p.191-191, Article 191

2017

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Nutritional Status Associated with Molecular Biomarkers, Physiological Indices, and Clinical Severity in Parkinson’s Disease Patients

International journal of environmental research and public health, 2020-08, Vol.17 (16), p.5727

2020

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Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement

Frontiers in neurology, 2022-09, Vol.13, p.1005670-1005670

2022

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Two Birds One Stone: The Neuroprotective Effect of Antidiabetic Agents on Parkinson Disease-Focus on Sodium-Glucose Cotransporter 2 (SGLT2) Inhibitors

Antioxidants, 2021-12, Vol.10 (12), p.1935

2021

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Investigating DYT1 in a Taiwanese dystonia cohort

Journal of the Formosan Medical Association, 2022-01, Vol.121 (1), p.375-380

2022

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Effect of erythropoietin on level of circulating endothelial progenitor cells and outcome in patients after acute ischemic stroke

Critical care (London, England), 2011-01, Vol.15 (1), p.R40-R40

2011

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Mitochondrial Transfer of Wharton’s Jelly Mesenchymal Stem Cells Eliminates Mutation Burden and Rescues Mitochondrial Bioenergetics in Rotenone-Stressed MELAS Fibroblasts

Oxidative medicine and cellular longevity, 2019-01, Vol.2019, p.9537504-17

2019

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Spastic paraparesis as the first manifestation of Machado-Joseph disease: A case report and review of the literature

Clinical neurology and neurosurgery, 2018-09, Vol.172, p.137-140

2018

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Spontaneous splenic rupture as the first clinical manifestation of Niemann-Pick disease type B: A case report and review of the literature

Journal of clinical lipidology, 2022-07, Vol.16 (4), p.434-437

2022

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A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan

The Journal of molecular diagnostics : JMD, 2022-03, Vol.24 (3), p.262-273

2022

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Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia

Parkinsonism & related disorders, 2023-02, Vol.107, p.105294-105294, Article 105294

2023

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Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan

Parkinsonism & related disorders, 2021-06, Vol.87, p.87-91

2021

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The Genetics of Primary Familial Brain Calcification: A Literature Review

Blood neurofilament light chain as a surrogate marker for dystonia

Miro1 improves the exogenous engraftment efficiency and therapeutic potential of mitochondria transfer using Wharton's jelly mesenchymal stem cells

Recessively‐Inherited Adult‐Onset Alexander Disease Caused by a Homozygous Mutation in the GFAP Gene

Iron Brain Menace: The Involvement of Ferroptosis in Parkinson Disease

Erythropoietin improves long-term neurological outcome in acute ischemic stroke patients: a randomized, prospective, placebo-controlled clinical trial

Higher prevalence of idiopathic normal pressure hydrocephalus‐like MRI features in progressive supranuclear palsy: An imaging reminder of atypical parkinsonism

Mitochondrial dysfunctions in leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation (LBSL)

Brain hypoperfusion and nigrostriatal dopaminergic dysfunction in primary familial brain calcification caused by novel MYORG variants: case report

Unraveling the Pathogenetic Mechanisms Underlying the Association between Specific Mitochondrial DNA Haplogroups and Parkinson's Disease

Genetic analysis of IRF2BPL in a Taiwanese dystonia cohort: The genotype and phenotype correlation

Glucagon-Like Peptide-1 Receptor Agonist Ameliorates 1-Methyl-4-Phenyl-1,2,3,6-Tetrahydropyridine (MPTP) Neurotoxicity Through Enhancing Mitophagy Flux and Reducing α-Synuclein and Oxidative Stress

Level and Value of Circulating Endothelial Progenitor Cells in Patients After Acute Ischemic Stroke

Identification of VPS35 p.D620N mutation-related Parkinson's disease in a Taiwanese family with successful bilateral subthalamic nucleus deep brain stimulation: a case report and literature review

Nutritional Status Associated with Molecular Biomarkers, Physiological Indices, and Clinical Severity in Parkinson’s Disease Patients

Clinical and genetic characterization of a Taiwanese cohort with spastic paraparesis combined with cerebellar involvement

Two Birds One Stone: The Neuroprotective Effect of Antidiabetic Agents on Parkinson Disease-Focus on Sodium-Glucose Cotransporter 2 (SGLT2) Inhibitors

Investigating DYT1 in a Taiwanese dystonia cohort

Effect of erythropoietin on level of circulating endothelial progenitor cells and outcome in patients after acute ischemic stroke

Mitochondrial Transfer of Wharton’s Jelly Mesenchymal Stem Cells Eliminates Mutation Burden and Rescues Mitochondrial Bioenergetics in Rotenone-Stressed MELAS Fibroblasts

Spastic paraparesis as the first manifestation of Machado-Joseph disease: A case report and review of the literature

Spontaneous splenic rupture as the first clinical manifestation of Niemann-Pick disease type B: A case report and review of the literature

A Clinical and Integrated Genetic Study of Isolated and Combined Dystonia in Taiwan

Genetic analysis of IMPDH2 gene in Taiwanese patients with isolated or combined dystonia

Clinical and genetic characterization of hereditary spastic paraplegia type 3A in Taiwan

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