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Parkinsonism
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Syndrome characterized by tremor, slowed movements, rigidity, and imbalance
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Subclasses 1
Influences rating
rare parkinsonian syndrome due to neurodegenerative disease
human disease
Subject of 7
Emerging Targeted Therapeutics for Genetic Subtypes of Parkinsonism
scientific article published on 10 September 2020
CHOP/GADD153 is a mediator of apoptotic death in substantia nigra dopamine neurons in an in vivo neurotoxin model of parkinsonism
scientific journal article
Longitudinal characterization of two siblings with frontotemporal dementia and parkinsonism linked to chromosome 17 associated with the S305N tau mutation.
scientific article published on 22 December 2004
Mutations in SLC30A10 Cause Parkinsonism and Dystonia with Hypermanganesemia, Polycythemia, and Chronic Liver Disease
scientific article published on February 16, 2012
Nucleolar Disruption in Dopaminergic Neurons Leads to Oxidative Damage and Parkinsonism through Repression of Mammalian Target of Rapamycin Signaling
scientific article published on 01 January 2011
Frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17)
scientific article
Mutations in LRRK2 cause autosomal-dominant parkinsonism with pleomorphic pathology
scientific article (publication date: 18 November 2004)
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Wikipedia

Parkinsonism is a clinical syndrome characterized by tremor, bradykinesia (slowed movements), rigidity, and postural instability.

Instance of
designated intractable/rare disease
class of disease
Syndrome
Subclass of
Movement disorder
References
Wikidata