(Q44764021)

6 December 2017

title

Association of variations in monoamine oxidases A and B with Parkinson's disease subgroups (English)

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6 December 2017

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5

Perlmutter JS

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6 December 2017

Parsian A

1

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6 December 2017

Racette B

series ordinal

2

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6 December 2017

Zhang ZH

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3

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6 December 2017

Rundle M

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4

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6 December 2017

publication date

1 March 2004

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6 December 2017

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6 December 2017

volume

83

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6 December 2017

issue

3

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6 December 2017

page(s)

454-460

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Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

6 December 2017

cites work

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.09.002

Mutation, sequence analysis, and association studies of alpha-synuclein in Parkinson's disease

7 January 2021

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Genetic Complexity and Parkinson's Disease

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Failure to find the alpha-synuclein gene missense mutation (G209A) in 100 patients with younger onset Parkinson's disease

7 January 2021

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Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

7 January 2021

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Association between early-onset Parkinson's disease and mutations in the parkin gene

7 January 2021

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Molecular genetics of the monoamine oxidases

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.09.002

Relationship between platelet monoamine oxidase B activity and alleles at the MAOB locus

7 January 2021

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The antiparkinson efficacy of deprenyl derives from transient improvement that is likely to be symptomatic

7 January 2021

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The effect of deprenyl and levodopa on the progression of Parkinson's disease

7 January 2021

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Parkinsonism in monkeys produced by chronic administration of an endogenous substance of the brain, tetrahydroisoquinoline: the behavioral and biochemical changes

7 January 2021

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Inhibition of [3H]dopamine uptake into striatal synaptosomes by isoquinoline derivatives structurally related to 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine

7 January 2021

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Platelet monoamine oxidase-B activity in Parkinson's disease

7 January 2021

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Association of a monoamine oxidase B allele with Parkinson's disease

7 January 2021

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An allelic association study of monoamine oxidase B in parkinson's disease

7 January 2021

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Association analysis of a polymorphism of the monoamine oxidase B gene with Parkinson's disease in a Japanese population

7 January 2021

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Hereditary variations in monoamine oxidase as a risk factor for Parkinson's disease

7 January 2021

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No association between Parkinson's disease and monoamine oxidase A and B gene polymorphisms.

7 January 2021

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https://api.crossref.org/works/10.1016%2FJ.YGENO.2003.09.002

Association of a polymorphism in intron 13 of the monoamine oxidase B gene with Parkinson disease.

7 January 2021

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Variations in the monoamine oxidase B (MAOB) gene are associated with Parkinson's disease.

7 January 2021

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MAOB intron 13 and COMT codon 158 polymorphisms, cigarette smoking, and the risk of PD

7 January 2021

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7 January 2021

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Evaluation of a screening questionnaire for genetic studies of Parkinson's disease

7 January 2021

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Accuracy of clinical diagnosis of idiopathic Parkinson's disease: a clinico-pathological study of 100 cases

7 January 2021

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Monoamine oxidases and alcoholism. I. Studies in unrelated alcoholics and normal controls.

7 January 2021

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Highly polymorphic (GT)n repeat sequence in intron II of the human MAOB gene

7 January 2021

1 reference

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10.1016/J.YGENO.2003.09.002

7 January 2021

Identifiers

DOI

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6 December 2017

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