Cardiac abnormalities in patients with mitochondrial DNA mutation 3243A&gt;G. (Q24799134)

4 July 2017

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

1 reference

4 July 2017

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Kirsi Majamaa-Voltti

1

1 reference

4 July 2017

Keijo Peuhkurinen

2

1 reference

4 July 2017

Marja-Leena Kortelainen

3

1 reference

4 July 2017

Ilmo E Hassinen

4

1 reference

4 July 2017

Kari Majamaa

5

1 reference

4 July 2017

language of work or name

English

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publication date

1 August 2002

1 reference

BMC Cardiovascular Disorders

4 July 2017

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4 July 2017

2

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4 July 2017

12

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describes a project that uses

4 July 2017

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2261-2-12

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cites work

Sequence and organization of the human mitochondrial genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Dilated cardiomyopathy and neonatal lethality in mutant mice lacking manganese superoxide dismutase

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes: A distinctive clinical syndrome

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Melas: an original case and clinical criteria for diagnosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Prognostic implications of echocardiographically determined left ventricular mass in the Framingham Heart Study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

The emerging concept of mitochondrial cardiomyopathies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Mitochondrial DNA mutations in the pathogenesis of human disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Mitochondrial myopathies: genetic mechanisms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Maternally inherited diabetes and deafness: a new diabetes subtype

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Cardiac involvement in mitochondrial diseases. A study on 17 patients with documented mitochondrial DNA defects

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Cardiomyopathy in the Kearns-Sayre syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

The prevalence and correlates of echocardiographic left ventricular hypertrophy among employed patients with uncomplicated hypertension

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Recommendations for quantitation of the left ventricle by two-dimensional echocardiography. American Society of Echocardiography Committee on Standards, Subcommittee on Quantitation of Two-Dimensional Echocardiograms

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Cardiomyopathies in disorders of oxidative metabolism

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Mitochondrial DNA mutations and pathogenesis

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

The mitochondrial A3243G mutation presenting as severe cardiomyopathy

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings.

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

A point mutation in the mitochondrial tRNA(Leu)(UUR) gene in MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes).

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS): a correlative study of the clinical features and mitochondrial DNA mutation

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Lumping or splitting? "Ophthalmoplegia-plus" or Kearns-Sayre syndrome?

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=119851

Clostridium difficile colitis

30 May 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

MELAS and MERRF. The relationship between maternal mutation load and the frequency of clinically affected offspring.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Epidemiologic assessment of the role of blood pressure in stroke: the Framingham Study. 1970.

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Transesophageal Echocardiography

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Maternally inherited myopathy and cardiomyopathy: association with mutation in mitochondrial DNA tRNALeu(UUR)

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Cardiomyopathy and angiopathy in patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Mitochondrial DNA defects in cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

An additional mitochondrial tRNA(Ile) point mutation (A-to-G at nucleotide 4295) causing hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Variants of renin-angiotensin system genes and echocardiographic left ventricular mass

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

A critical appraisal of the electrocardiographic criteria for the diagnosis of left ventricular hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

A mouse model for mitochondrial myopathy and cardiomyopathy resulting from a deficiency in the heart/muscle isoform of the adenine nucleotide translocator

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Increased activities of antioxidant enzymes and decreased ATP concentration in cultured myoblasts with the 3243A-->G mutation in mitochondrial DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1186%2F1471-2261-2-12

Inherited cardiomyopathies

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12150714

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1471-2261-2-12

1 reference

Dimensions Publication ID

4 July 2017

0 references

1 reference

4 July 2017

1 reference