(Q43975266)

28 November 2017

title

Parkinson syndrome as a manifestation of mitochondriopathy (English)

1 reference

28 November 2017

1 reference

Finsterer J

1

1 reference

28 November 2017

language of work or name

English

0 references

publication date

1 May 2002

1 reference

Acta Neurologica Scandinavica

28 November 2017

published in

1 reference

28 November 2017

volume

105

1 reference

28 November 2017

issue

5

1 reference

28 November 2017

page(s)

384-389

1 reference

Mitochondrial myopathies and encephalomyopathies

28 November 2017

cites work

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

The natural history of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Interaction among mitochondria, mitogen-activated protein kinases, and nuclear factor-kappaB in cellular models of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Use of cytoplasmic hybrid cell lines for elucidating the role of mitochondrial dysfunction in Alzheimer's disease and Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial DNA transmission of the mitochondrial defect in Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Matrilineal inheritance of complex I dysfunction in a multigenerational Parkinson's disease family

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

A novel mitochondrial 12SrRNA point mutation in parkinsonism, deafness, and neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Abnormal mitochondrial morphology in sporadic Parkinson's and Alzheimer's disease cybrid cell lines

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Phenotype variability in 130 adult patients with respiratory chain disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial respiratory chain disorders I: mitochondrial DNA defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial respiratory chain disorders II: neurodegenerative disorders and nuclear gene defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Genetic influence on the development of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Pathoanatomy of Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Parkinson's disease is associated with oxidative damage to cytoplasmic DNA and RNA in substantia nigra neurons

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Dopamine oxidation alters mitochondrial respiration and induces permeability transition in brain mitochondria: implications for Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial impairment as an early event in the process of apoptosis induced by glutathione depletion in neuronal cells: relevance to Parkinson's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

Mitochondrial encephalomyopathies: back to Mendelian genetics.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

CNS involvement in primary Sjögren's syndrome: a case with a clue for the pathogenesis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

A 4-base pair deletion in the mitochondrial cytochrome b gene associated with parkinsonism/MELAS overlap syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

1 reference

7 January 2021

Mitochondrial dysfunction in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

Detection of respiratory chain defects in cultivated skin fibroblasts and skeletal muscle of patients with Parkinson's disease

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

Visually evoked potentials in respiratory chain disorders

1 reference

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

7 January 2021

https://api.crossref.org/works/10.1034%2FJ.1600-0404.2002.01221.X

1 reference

7 January 2021

10.1034/J.1600-0404.2002.01221.X

Identifiers

DOI

1 reference

28 November 2017

1 reference