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Nigrostriatal dysfunction in homozygous and heterozygous parkin gene carriers: An 18F-dopa PET progression study
Movement Disorders, 11/03/09
Pavese N et al. – Although subclinical reductions of striatal 18F–dopa uptake are common in carriers of a single parkin mutation their slow rate of progression suggests that few if any of these will develop clinical parkinsonism.
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Today in Basic Science/Genetics...keeping you current
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Skeletal dysplasias due to filamin A mutations result from a gain-of-function mechanism distinct from allelic neurological disorders
Human Molecular Genetics, 11/24/09
Gene Expression Analysis of Tuberous Sclerosis Complex Cortical Tubers Reveals Increased Expression of Adhesion and Inflammatory Factors
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Today in Movement Disorders...keeping you current
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Pediatric Constraint-Induced Movement Therapy: A Promising Intervention for Childhood Hemiparesis
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Combined Damage to the Right Hemispheric Hand Area in the Primary Motor and Sensory Area Plays a Critical Role in Motor Hemineglect
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