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The Journal of Cell Biology, ISSN 0021-9525, 4/2010, Volume 189, Issue 2, pp. 211 - 221
Parkinson's disease (PD) is a prevalent neuro-degenerative disorder. Recent identification of genes linked to familial forms of PD such as Parkin and PINK1... 
Mitochondria | Report | Ubiquitins | Mitochondrial membranes | HeLa cells | Parkinson disease | Antibodies | Immunoblotting | Genetic mutation | Cytoplasm | Perceptual localization | UBIQUITIN-PROTEIN LIGASE | DISEASE | DEGRADATION | PROTEASOME SYSTEM | MUTATIONS | DYSFUNCTION | AUTOPHAGY | RECESSIVE PARKINSONISM | DROSOPHILA-PINK1 | IMPAIRMENT | CELL BIOLOGY | Protein Kinases - metabolism | Protein Kinases - genetics | Uncoupling Agents - pharmacology | Humans | Fluorescent Dyes - metabolism | Dimethyl Sulfoxide - pharmacology | Mitochondrial Proteins - genetics | Recombinant Fusion Proteins - metabolism | Solvents - pharmacology | Mitochondrial Proteins - metabolism | Carbonyl Cyanide m-Chlorophenyl Hydrazone - pharmacology | Membrane Potential, Mitochondrial - physiology | Parkinson Disease - metabolism | Fibroblasts - metabolism | Biomarkers - metabolism | Parkinson Disease - pathology | Ubiquitin-Protein Ligases - metabolism | Receptors, Cytoplasmic and Nuclear - genetics | Mitochondria - drug effects | Mitochondria - pathology | Mice, Knockout | Animals | Recombinant Fusion Proteins - genetics | Fibroblasts - cytology | Mice | HeLa Cells | Mitochondria - physiology | Ubiquitin-Protein Ligases - genetics | Receptors, Cytoplasmic and Nuclear - metabolism | Ubiquitin | Properties | Mitochondrial DNA | Enzymes | Membranes | Cellular biology | Parkinsons disease | Gene expression | Index Medicus
Journal Article
Autophagy, ISSN 1554-8627, 02/2011, Volume 7, Issue 2, pp. 176 - 187
Journal Article
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 08/2015, Volume 21, Issue 8, pp. 911 - 916
Introduction: Mitochondrial complex I deficiencies have been found in post-mortem brains of patients with Parkinson's disease (PD). Coenzyme Q 10 (CoQ 10 ) is... 
Oxidative stress | Parkinson's disease | Complex I | Reduced form of coenzyme Q10 | Randomized controlled trial
Journal Article
BMC neurology, ISSN 1471-2377, 02/2017, Volume 17, Issue 1, pp. 35 - 35
  After publication of the original article [1], it came to the authors' attention that there was an error in the number of male and female participants. The... 
Parkinsons disease
Journal Article
Journal of Neural Transmission, ISSN 0300-9564, 6/2018, Volume 125, Issue 6, pp. 937 - 944
Coenzyme Q2, polyprenyltransferase (COQ2) variants have been reported to be associated with multiple system atrophy (MSA). However, the relationship between... 
Neurology | Neurosciences | COQ2 | Medicine & Public Health | familial Parkinson’s disease | Genetics | multiple system atrophy | Psychiatry
Journal Article
Case Reports in Neurology, ISSN 1662-680X, 03/2015, Volume 7, Issue 1, pp. 59 - 62
Introduction: Painless legs and moving toes syndrome (PoLMT) is a rare movement disorder characterized by flexion, extension, abduction, adduction, and torsion... 
Published: March 2015 | Moving toes | Painful legs | Painless legs | Clonazepam
Journal Article
Case reports in neurological medicine, ISSN 2090-6668, 2016, Volume 2016, pp. 6829410 - 6829410
Painless Legs and Moving Toes Syndrome (PoLMT) is a rare movement disorder characterized by flexion, extension, abduction, adduction, and torsion of toes... 
Hostages | Parkinson's disease | Spinal cord | Hospitals | Pain | Dopamine | Parkinsons disease | Hallucinations | Family medical history | Case Report
Journal Article
Case Reports in Neurological Medicine, ISSN 2090-6668, 2016, Volume 2016, pp. 1 - 2
Painless Legs and Moving Toes Syndrome (PoLMT) is a rare movement disorder characterized by flexion, extension, abduction, adduction, and torsion of toes... 
Journal Article
JOURNAL OF NEURAL TRANSMISSION, ISSN 0300-9564, 06/2018, Volume 125, Issue 6, pp. 937 - 944
Coenzyme Q2, polyprenyltransferase (COQ2) variants have been reported to be associated with multiple system atrophy (MSA). However, the relationship between... 
PARA-HYDROXYBENZOATE | DIAGNOSIS | COQ2 | PATHOGENICITY | familial Parkinson's disease | MITOCHONDRIAL ENCEPHALOMYOPATHY | Genetics | RISK | multiple system atrophy | COENZYME Q DEFICIENCY | NEUROSCIENCES | CLINICAL NEUROLOGY | Atrophy | Enzymes | Medical colleges | Medical research | Medicine, Experimental | Medical records | Research institutes
Journal Article
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