selected publications
- Combination Disease-Modifying Therapy for Neurodegenerative Diseases Using Repurposed Drugs. Annals of neurology. 2026 Information Resource GET IT
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Combination Supplement Therapy: A New Frontier in Treatment of Neurodegenerative Diseases.
The Journal of nutrition.
2025
Information Resource
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Times cited: 1 -
Evaluation of Additive Neuroprotective Effect of Combination Therapy for Parkinson's Disease Using In Vitro Models.
Antioxidants (Basel, Switzerland).
2025
Academic Article
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Times cited: 2 -
Combination of tauroursodeoxycholic acid, co-enzyme Q10 and creatine demonstrates additive neuroprotective effects in in-vitro models of Parkinson's disease.
Frontiers in neuroscience.
2024
Academic Article
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Times cited: 8 -
Quantitative evaluation of brain iron accumulation in different stages of Parkinson's disease.
Journal of neuroimaging : official journal of the American Society of Neuroimaging.
2021
Academic Article
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Times cited: 42 - Restabilization treatment after intravenous immunoglobulin withdrawal in chronic inflammatory demyelinating polyneuropathy: Results from the pre-randomization phase of the Polyneuropathy And Treatment with Hizentra study. Journal of the Peripheral Nervous System. 2019 Article GET IT
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Prevalence of pain in atypical parkinsonism: a systematic review and meta-analysis.
Journal of neurology.
2018
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Times cited: 20 -
Clinical quantitative susceptibility mapping (QSM): Biometal imaging and its emerging roles in patient care.
Journal of magnetic resonance imaging : JMRI.
2017
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Times cited: 248 -
Quantitative susceptibility mapping of the motor cortex in amyotrophic lateral sclerosis and primary lateral sclerosis.
AJR. American journal of roentgenology.
2015
Academic Article
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Times cited: 77 -
Perioperative management of patients with Parkinson's disease.
The American journal of medicine.
2013
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Times cited: 42 -
Biomarkers in Parkinson's disease: an update.
Current opinion in neurology.
2012
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Times cited: 58 -
Differential gene expression in patients with amyotrophic lateral sclerosis.
Amyotrophic lateral sclerosis : official publication of the World Federation of Neurology Research Group on Motor Neuron Diseases.
2011
Academic Article
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Times cited: 30 -
G8363A mutation in the mitochondrial DNA transfer ribonucleic acidLys gene: another cause of Leigh syndrome.
Journal of child neurology.
2000
Article
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Times cited: 47 -
A novel mutation in the mitochondrial DNA transfer ribonucleic acidAsp gene in a child with myoclonic epilepsy and psychomotor regression.
Journal of child neurology.
1999
Article
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Times cited: 24 -
A nonsense mutation (G15059A) in the cytochrome b gene in a patient with exercise intolerance and myoglobinuria.
Annals of neurology.
1999
Article
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Times cited: 96 -
Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy.
Neurology.
1998
Article
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Times cited: 77 -
Isolation and characterization of a new gene encoding a member of the HIRA family of proteins from Drosophila melanogaster.
Gene.
1998
Academic Article
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Times cited: 33 -
Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes.
Proceedings of the National Academy of Sciences of the United States of America.
1997
Academic Article
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Times cited: 116