(Q21093316)

15 August 2022

4

Anna Olivieri

Anna

Olivieri

1 reference

15 August 2022

Francesca Gandini

3

Francesca

Gandini

1 reference

15 August 2022

Leonardo Caporali

2

Leonardo

Caporali

1 reference

15 August 2022

Raffaele Lodi

12

Raffaele

Lodi

1 reference

15 August 2022

Carlotta Stipa

8

Carlotta

Stipa

1 reference

15 August 2022

Chiara La Morgia

1

Chiara

La Morgia

1 reference

15 August 2022

Caterina Tonon

11

Caterina

Tonon

1 reference

15 August 2022

Valerio Carelli

14

Valerio

Carelli

1 reference

15 August 2022

Francesco Toni

5

Francesco

Toni

1 reference

15 August 2022

Stefania Nassetti

6

Stefania

Nassetti

1 reference

15 August 2022

Daniela Brunetto

7

Daniela

Brunetto

1 reference

15 August 2022

Cristina Scaduto

9

Cristina

Scaduto

1 reference

15 August 2022

Antonia Parmeggiani

10

Antonia

Parmeggiani

1 reference

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

15 August 2022

language of work or name

English

0 references

publication date

2014

0 references

published in

BMC Neurology

0 references

volume

14

0 references

issue

1

0 references

page(s)

116

0 references

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Mitochondrial dysfunction as a cause of optic neuropathies

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Cybrid studies establish the causal link between the mtDNA m.3890G>A/MT-ND1 mutation and optic atrophy with bilateral brainstem lesions

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

The optic nerve: a "mito-window" on mitochondrial neurodegeneration

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Oxidative phosphorylation differences between mitochondrial DNA haplogroups modify the risk of Leber's hereditary optic neuropathy

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Oestrogens ameliorate mitochondrial dysfunction in Leber's hereditary optic neuropathy.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Haplogroup effects and recombination of mitochondrial DNA: novel clues from the analysis of Leber hereditary optic neuropathy pedigrees.

12 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4047257

Leigh-like encephalopathy complicating Leber's hereditary optic neuropathy.

12 September 2017

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-14-116

A common pattern of brain MRI imaging in mitochondrial diseases with complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-14-116

Rare mtDNA variants in Leber hereditary optic neuropathy families with recurrence of myoclonus.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-14-116

Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-14-116

Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2377-14-116

21 January 2018

Identifiers

DOI

10.1186/1471-2377-14-116

0 references