Parkinson's disease: current and future challenges (Q33337881)

25 July 2017

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title

Parkinson's disease: current and future challenges (English)

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25 July 2017

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J William Langston

1

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25 July 2017

1 October 2002

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25 July 2017

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25 July 2017

23

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25 July 2017

4-5

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25 July 2017

443-450

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A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility in Parkinson's Disease

25 July 2017

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Absence of mutations in the coding region of the alpha-synuclein gene in pathologically proven Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

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

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Concurrence of alpha-synuclein and tau brain pathology in the Contursi kindred

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Kindreds of dominantly inherited Parkinson's disease: keys to the riddle

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Lewy bodies and parkinsonism in families with parkin mutations

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Spinocerebellar ataxia type 1 with multiple system degeneration and glial cytoplasmic inclusions

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

A large kindred with autosomal dominant Parkinson's disease

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Clinical genetic analysis of Parkinson's disease in the Contursi kindred

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Positron emission tomography reveals strong genetic influence in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Smoking and Parkinson's disease: a dose-response relationship.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Prospective study of cigarette smoking and the risk of developing idiopathic Parkinson's disease

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Molecular genetic analysis of a novelParkin gene in Japanese families with autosomal recessive juvenile parkinsonism: Evidence for variable homozygous deletions in theParkin gene in affected individuals

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Ala30Pro mutation in the gene encoding alpha-synuclein in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Chronic Parkinsonism in humans due to a product of meperidine-analog synthesis

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Novel alpha-synuclein-immunoreactive proteins in brain samples from the Contursi kindred, Parkinson's, and Alzheimer's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

The ubiquitin pathway in Parkinson's disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Homozygous deletions in parkin gene in European and North African families with autosomal recessive juvenile parkinsonism. The European Consortium on Genetic Susceptibility in Parkinson's Disease and the French Parkinson's Disease Genetics Study Gro

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Parkinson's disease. A genetic study

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

The role of inheritance in sporadic Parkinson's disease: evidence from a longitudinal study of dopaminergic function in twins.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

COHORT ANALYSIS OF PARKINSON'S SYNDROME: EVIDENCE FOR A SINGLE ETIOLOGY RELATED TO SUBCLINICAL INFECTION ABOUT 1920.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Bias in analytic research

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

alpha-Synuclein in filamentous inclusions of Lewy bodies from Parkinson's disease and dementia with lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Alpha-synuclein in Lewy bodies

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Epidemiology of Parkinson's disease.

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Parkinson disease in twins: an etiologic study

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Familial juvenile parkinsonism: clinical and pathologic study in a family.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

The alpha-synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: a study of 230 European cases. European Consortium on Genetic Susceptibility in Parkinson's Disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Parkinson's disease in 65 pairs of twins and in a set of quadruplets

1 reference

https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

Paralysis agitans of early onset with marked diurnal fluctuation of symptoms

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https://api.crossref.org/works/10.1016%2FS0161-813X%2802%2900098-0

7 January 2021

10.1016/S0161-813X(02)00098-0

Identifiers

DOI

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25 July 2017

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PubMed ID

12428715