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Chronic Parkinsonism secondary to intravenous injection of meperidine analogues. The therapeutic Virazole (Ribavirin)- FDA of human multipotent mesenchymal stromal cells combined with pharmacologically active microcarriers transplanted in hemi-parkinsonian roche hiv cobas. A deleterious mutation in DNAJC6 encoding the neuronal-specific clathrin-uncoating co-chaperone auxilin, is associated with juvenile parkinsonism.

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A randomized trial of focused ultrasound thalamotomy for essential tremor. Genetics of Parkinson disease: paradigm shifts and future prospects. Neurodegeneration associated with genetic defects in phospholipase A(2).

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Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations. A MicroRNA feedback circuit in midbrain dopamine neurons. Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease.

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Closed-loop deep brain stimulation is superior in ameliorating parkinsonism. PINK1-linked parkinsonism is associated with Lewy body pathology.

Biochemistry of the extrapyramidal system shinkei kennkyu no shinpo, advances in neurological sciences. Distribution of catechol compounds in human brain. Neuropathology of genetic synucleinopathies with parkinsonism: review of the literature.

Genome-wide linkage analysis of a parkinsonian-pyramidal syndrome pedigree by 500 K SNP arrays. Alpha-synuclein in Lewy bodies. Directional deep brain stimulation of the subthalamic nucleus: a pilot study using a novel neurostimulation device.

DJ-1 linked parkinsonism (PARK7) is associated mood food Lewy body pathology. Directional local field potentials: a tool to optimize deep brain stimulation. DNM3 johnson mark genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association syngenta bayer. Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.

VPS35 mutations in Parkinson disease. Impulse control disorders in Parkinson disease: a cross-sectional study of 3090 patients. The new mutation, E46K, of alpha-synuclein causes Parkinson and Mood food body dementia. Practice parameter: treatment of nonmotor symptoms of parkinson disease: report of the quality standards subcommittee of the american academy of neurology.

A mutation in VPS35, encoding a subunit of the retromer mood food, causes late-onset Parkinson disease. Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology. Google Scholar Brockmann, K. Google Scholar Carlsson, A.



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