Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease (Q36855295)

16 August 2017

title

Mitochondrial DNA polymorphisms in pathologically proven Parkinson's disease (English)

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16 August 2017

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4

Marsden CD

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16 August 2017

1

O Bandmann

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2

M G Sweeney

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3

S E Daniel

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5

N W Wood

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publication date

1 April 1997

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16 August 2017

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volume

244

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issue

4

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16 August 2017

page(s)

262-265

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A large kindred with autosomal dominant Parkinson's disease

16 August 2017

cites work

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https://api.crossref.org/works/10.1007%2FS004150050082

Low platelet mitochondrial complex I and complex II/III activity in early untreated Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Neurological disease and mitochondrial genes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

A clinical genetic study of Parkinson's disease: evidence for dominant transmission

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Normal mitochondrial genome in brain from patients with Parkinson's disease and complex I defect

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Quantitation of a mitochondrial DNA deletion in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

The clinical features of mitochondrial myopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

PCR analysis of platelet mtDNA: lack of specific changes in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Possible environmental, occupational, and other etiologic factors for Parkinson's disease: a case-control study in Germany.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Movement disorders in mitochondrial myopathies. A study of nine cases with two autopsy studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS004150050082

Smoking and mitochondrial function: a model for environmental toxins

21 January 2018

1 reference

12 December 2020

Distinct clustering of point mutations in mitochondrial DNA among patients with mitochondrial encephalomyopathies and with Parkinson's disease

1 reference

12 December 2020

Electron transfer complexes I and IV of platelets are abnormal in Parkinson's disease but normal in Parkinson-plus syndromes.

1 reference

12 December 2020

A new mitochondrial disease associated with mitochondrial DNA heteroplasmy

1 reference

12 December 2020

A Greek-American kindred with autosomal dominant, levodopa-responsive parkinsonism and anticipation

1 reference

12 December 2020

Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism

1 reference

12 December 2020

Investigations on the point mutations at nt 5460 of the mtDNA in different neurodegenerative and neuromuscular diseases

1 reference

12 December 2020

[Hereditary Parkinson disease: report of 3 families with dominant autosomal inheritance]

1 reference

12 December 2020

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

1 reference

12 December 2020

A new mitochondrial DNA mutation associated with progressive dementia and chorea: A clinical, pathological, and molecular genetic study

1 reference

12 December 2020

A clinical and genetic study of familial Parkinson's disease

1 reference

12 December 2020

1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging

1 reference

12 December 2020

Mitochondrial DNA analysis in Parkinson's disease

1 reference

12 December 2020

Mitochondrial complex I deficiency in Parkinson's disease

1 reference

12 December 2020

The oxidative inactivation of mitochondrial electron transport chain components and ATPase.

1 reference

12 December 2020

Identifiers

DOI

10.1007/S004150050082

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16 August 2017

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