(Q34647096)

3 August 2017

title

Mitochondrial DNA haplogroups and mutations in children with acquired central demyelination (English)

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3 August 2017

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S Venkateswaran

1

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3 August 2017

K Zheng

2

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3 August 2017

M Sacchetti

3

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3 August 2017

D Gagne

4

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3 August 2017

D L Arnold

5

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3 August 2017

A D Sadovnick

6

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3 August 2017

S W Scherer

7

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3 August 2017

B Banwell

8

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3 August 2017

A Bar-Or

9

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3 August 2017

D K Simon

10

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3 August 2017

Canadian Pediatric Demyelinating Disease Network

11

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3 August 2017

language of work or name

English

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publication date

2 February 2011

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3 August 2017

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3 August 2017

volume

76

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3 August 2017

issue

9

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3 August 2017

page(s)

774-780

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Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

3 August 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Incidence of acquired demyelination of the CNS in Canadian children

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial disease in autism spectrum disorder patients: a cohort analysis

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Association of common mitochondrial DNA variants with multiple sclerosis and systemic lupus erythematosus

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

The involvement of mitochondria in the pathogenesis of multiple sclerosis.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Consensus definitions proposed for pediatric multiple sclerosis and related disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

mtDNA mutations and common neurodegenerative disorders

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial DNA mutations in human disease.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial disorders: clinical and genetic features

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber hereditary optic neuropathy and hereditary spastic dystonia

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

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

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial complex I gene variant associated with early age at onset in spinocerebellar ataxia type 2.

7 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial DNA haplogroup cluster UKJT reduces the risk of PD.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Neuropathology of white matter disease in Leber's hereditary optic neuropathy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial DNA abnormalities and autistic spectrum disorders.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Visual recovery in a man with the rare combination of mtDNA 11778 LHON mutation and a MS-like disease after mitoxantrone therapy

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

White matter abnormalities in Leber's hereditary optic neuropathy due to the 3460 mitochondrial DNA mutation

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Prospective study of multiple sclerosis with early onset

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Mitochondrial mutations of Leber's hereditary optic neuropathy: a risk factor for multiple sclerosis.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Autism associated with the mitochondrial DNA G8363A transfer RNA(Lys) mutation.

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

Multiple sclerosis in childhood: clinical features of 149 cases

26 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3053335

mtDNA haplogroup J: a contributing factor of optic neuritis

26 October 2018

1 reference

12 December 2020

Mitochondrial DNA mutations in complex I and tRNA genes in Parkinson's disease

1 reference

12 December 2020

Oxidative damage to mitochondrial DNA and activity of mitochondrial enzymes in chronic active lesions of multiple sclerosis

1 reference

12 December 2020

Leber's hereditary optic neuropathy mitochondrial DNA mutations in childhood multiple sclerosis

1 reference

12 December 2020

Characterization of the mitochondrial DNA in patients with multiple sclerosis

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis patients with severe optic involvement

1 reference

12 December 2020

Mitochondrial DNA mutations in multiple sclerosis

1 reference

12 December 2020

A novel mitochondrial DNA point mutation in the tRNA(Ile) gene: studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis

1 reference

12 December 2020

Characterization of the mitochondrial genome in childhood multiple sclerosis. I. Optic neuritis and LHON mutations

1 reference

12 December 2020

Is the mitochondrial DNA involved in determining susceptibility to multiple sclerosis?

1 reference

12 December 2020

Large scale screening of the mitochondrial DNA reveals no pathogenic mutations but a haplotype associated with multiple sclerosis in Caucasians

1 reference

12 December 2020

Characterization of the mitochondrial genome in childhood multiple sclerosis. II. Multiple sclerosis without optic neuritis and LHON-associated genes

1 reference

12 December 2020

10.1212/WNL.0B013E31820EE1BB

Identifiers

DOI

1 reference

3 August 2017

1 reference

3 August 2017

1 reference