(Q36069669)

12 August 2017

Cardiomyopathy is common in patients with the mitochondrial DNA m.3243A>G mutation and correlates with mutation load (English)

1 reference

12 August 2017

0 references

1 reference

9

Patrick F Chinnery

1 reference

12 August 2017

2

Grainne S Gorman

1 reference

12 August 2017

Robert William Taylor

series ordinal

5

object named as

Robert W Taylor

1 reference

Douglass Matthew Turnbull

12 August 2017

series ordinal

6

object named as

Douglass M Turnbull

1 reference

12 August 2017

3

Michael I Trenell

1 reference

12 August 2017

8

Andrew M Blamire

1 reference

12 August 2017

Kieren G Hollingsworth

series ordinal

1

object named as

Kieren G Hollingsworth

1 reference

12 August 2017

7

Guy A MacGowan

1 reference

12 August 2017

4

Robert McFarland

1 reference

12 August 2017

17 April 2012

1 reference

12 August 2017

Neuromuscular Disorders

1 reference

12 August 2017

22

1 reference

12 August 2017

7

1 reference

12 August 2017

592-596

1 reference

Metoprolol reverses left ventricular remodeling in patients with asymptomatic systolic dysfunction: the REversal of VEntricular Remodeling with Toprol-XL (REVERT) trial

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A>G.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes (MELAS): current concepts

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Reversal of a mitochondrial DNA defect in human skeletal muscle.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

A novel heteroplasmic tRNAleu(CUN) mtDNA point mutation in a sporadic patient with mitochondrial encephalomyopathy segregates rapidly in skeletal muscle and suggests an approach to therapy.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Causes of death in pedigrees with the 3243A>G mutation in mitochondrial DNA.

11 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Prevalence, segregation, and phenotype of the mitochondrial DNA 3243A>G mutation in children.

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Depletion of mitochondrial DNA in leucocytes harbouring the 3243A->G mtDNA mutation

23 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3387369

Adult-onset hypertrophic cardiomyopathy manifested as initial major presentation of mitochondrial disease with A-to-G 3243 tRNA (Leu(UUR)) point mutation

23 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22513320

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Progressive depletion of mtDNA in mitochondrial myopathy

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22513320

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1016/J.NMD.2012.03.001

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

22513320

1 reference