Parkinsonian Disorders

"Parkinsonian Disorders" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure, which enables searching at various levels of specificity.

MeSH information

Definition | Details | More General Concepts | Related Concepts | More Specific Concepts

A group of disorders which feature impaired motor control characterized by bradykinesia, MUSCLE RIGIDITY; TREMOR; and postural instability. Parkinsonian diseases are generally divided into primary parkinsonism (see PARKINSON DISEASE), secondary parkinsonism (see PARKINSON DISEASE, SECONDARY) and inherited forms. These conditions are associated with dysfunction of dopaminergic or closely related motor integration neuronal pathways in the BASAL GANGLIA.

Descriptor ID	D020734
MeSH Number(s)	C10.228.140.079.862 C10.228.662.600
Concept/Terms	Parkinsonian Disorders Parkinsonian Disorders Parkinsonian Syndrome Parkinsonism Parkinsonian Syndromes Parkinsonian Diseases Autosomal Dominant Parkinsonism Autosomal Dominant Parkinsonism Dominant Parkinsonism, Autosomal Parkinsonism, Autosomal Dominant Autosomal Recessive Juvenile Parkinson Disease Autosomal Recessive Juvenile Parkinson Disease Chromosome 6-Linked Autosomal Recessive Parkinsonism Chromosome 6 Linked Autosomal Recessive Parkinsonism Familial Parkinson Disease, Autosomal Recessive Juvenile Parkinson Disease, Autosomal Recessive Juvenile Parkinsonism, Autosomal Recessive Parkinsonism, Early Onset, with Diurnal Fluctuation Parkinsonism, Juvenile, Autosomal Recessive Parkinson Disease 2, Autosomal Recessive Juvenile Parkinsonism, Early-Onset, With Diurnal Fluctuation Parkinson Disease, Juvenile, Autosomal Recessive Parkinson Disease 2 Parkinson Disease Autosomal Recessive, Early Onset Autosomal Recesssive Juvenile Parkinsonism Parkinson Disease, Familial, Autosomal Recessive Ramsay Hunt Paralysis Syndrome Ramsay Hunt Paralysis Syndrome Familial Juvenile Parkinsonism Familial Juvenile Parkinsonism Juvenile Parkinsonism, Familial Parkinsonism, Familial Juvenile Parkinsonism, Experimental Parkinsonism, Experimental Experimental Parkinsonisms Parkinsonisms, Experimental Parkinson Disease, Experimental Experimental Parkinsonism, MPTP-Induced Experimental Parkinsonism, MPTP Induced Parkinsonism, MPTP-Induced Experimental MPTP-Induced Experimental Parkinsonism MPTP Induced Experimental Parkinsonism Experimental Parkinson Disease Diseases, Experimental Parkinson Experimental Parkinson Diseases Parkinson Diseases, Experimental Experimental Parkinsonism Parkinsonism, Juvenile Parkinsonism, Juvenile Juvenile Parkinsonism Juvenile Parkinsonisms Parkinsonisms, Juvenile Parkinson Disease, Juvenile Juvenile Parkinson Disease Autosomal Dominant Juvenile Parkinson Disease Autosomal Dominant Juvenile Parkinson Disease Juvenile Parkinson Disease, Autosomal Dominant Parkinsonism, Juvenile, Autosomal Dominant Parkinson Disease, Autosomal Dominant. Juvenile Parkinson Disease, Juvenile, Autosomal Dominant Autosomal Dominant Juvenile Parkinsonism Juvenile Parkinsonism, Autosomal Dominant Autosomal Recessive Parkinsonism Autosomal Recessive Parkinsonism Parkinsonism, Autosomal Recessive Recessive Parkinsonism, Autosomal

Below are MeSH descriptors whose meaning is more general than "Parkinsonian Disorders".

Diseases [C]
Nervous System Diseases [C10]
Central Nervous System Diseases [C10.228]
Brain Diseases [C10.228.140]
Basal Ganglia Diseases [C10.228.140.079]
Parkinsonian Disorders [C10.228.140.079.862]
Movement Disorders [C10.228.662]
Parkinsonian Disorders [C10.228.662.600]

Below are MeSH descriptors whose meaning is more specific than "Parkinsonian Disorders".

publications

Timeline | Most Recent

This graph shows the total number of publications written about "Parkinsonian Disorders" by people in this website by year, and whether "Parkinsonian Disorders" was a major or minor topic of these publications.

Bar chart showing 52 publications over 20 distinct years, with a maximum of 6 publications in 2019

To see the data from this visualization as text, click here.

Year	Major Topic	Minor Topic	Total
2000	1	0	1
2001	1	0	1
2003	3	1	4
2004	1	1	2
2005	3	1	4
2006	0	1	1
2007	1	1	2
2008	2	1	3
2009	0	1	1
2010	0	2	2
2011	3	0	3
2012	2	0	2
2013	1	0	1
2014	3	0	3
2015	2	1	3
2016	5	0	5
2017	1	0	1
2018	3	0	3
2019	4	2	6
2021	4	0	4

Below are the most recent publications written about "Parkinsonian Disorders" by people in Profiles.

Jankovic J, Truong DD, Bologna M. Editorial "Parkinsonism across the spectrum of movement disorders and beyond". J Neurol Sci. 2022 Feb 15; 433:120013.

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Bologna M, Truong D, Jankovic J. The etiopathogenetic and pathophysiological spectrum of parkinsonism. J Neurol Sci. 2022 Feb 15; 433:120012.

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Bellows S, Jankovic J. Parkinsonism and tremor syndromes. J Neurol Sci. 2022 Feb 15; 433:120018.

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O'Shea SA, Hickman RA, Cortes E, Vonsattel JP, Fahn S, Okur V, Alcalay RN, Chung WK. Neuropathological Findings in a Case of Parkinsonism and Developmental Delay Associated with a Monoallelic Variant in PLXNA1. Mov Disord. 2021 11; 36(11):2681-2687.

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Bailey M, Shulman LM, Ryan D, Ouyang B, Shulman JM, Buchman AS, Bennett DA, Barnes LL, Hall DA. Frequency of Parkinsonism and Parkinson Disease in African Americans in the Chicago Community. J Gerontol A Biol Sci Med Sci. 2021 06 14; 76(7):1340-1345.

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Buchman AS, Yu L, Oveisgharan S, Farfel JM, Schneider JA, Bennett DA. Person-Specific Contributions of Brain Pathologies to Progressive Parkinsonism in Older Adults. J Gerontol A Biol Sci Med Sci. 2021 03 31; 76(4):615-621.

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Oubre B, Daneault JF, Whritenour K, Khan NC, Stephen CD, Schmahmann JD, Lee SI, Gupta AS. Decomposition of Reaching Movements Enables Detection and Measurement of Ataxia. Cerebellum. 2021 Dec; 20(6):811-822.

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Kim CY, Wirth T, Hubsch C, Németh AH, Okur V, Anheim M, Drouot N, Tranchant C, Rudolf G, Chelly J, Tatton-Brown K, Blauwendraat C, Vonsattel JPG, Cortes E, Alcalay RN, Chung WK. Reply to "PPP2R5D Genetic Mutations and Early Onset Parkinsonism". Ann Neurol. 2021 01; 89(1):195-196.

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Kim CY, Wirth T, Hubsch C, Németh AH, Okur V, Anheim M, Drouot N, Tranchant C, Rudolf G, Chelly J, Tatton-Brown K, Blauwendraat C, Vonsattel JPG, Cortes E, Alcalay RN, Chung WK. Early-Onset Parkinsonism Is a Manifestation of the PPP2R5D p.E200K Mutation. Ann Neurol. 2020 11; 88(5):1028-1033.

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Oveisgharan S, Dawe RJ, Leurgans SE, Yu L, Schneider JA, Bennett DA, Buchman AS. Total daily physical activity, brain pathologies, and parkinsonism in older adults. PLoS One. 2020; 15(4):e0232404.

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