(Q40519911)

21 September 2017

1 reference

title

Cardiomyopathy in respiratory chain disorders (English)

1 reference

21 September 2017

Guenthard J

1

1 reference

21 September 2017

Wyler F

series ordinal

2

1 reference

21 September 2017

Fowler B

series ordinal

3

1 reference

21 September 2017

Baumgartner R

series ordinal

4

1 reference

21 September 2017

language of work or name

English

0 references

publication date

1 March 1995

1 reference

Archives of Disease in Childhood

21 September 2017

1 reference

21 September 2017

72

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21 September 2017

3

1 reference

21 September 2017

223-226

1 reference

Mitochondrial myopathies. Clinical, morphological and biochemical aspects

21 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Hypertrophic cardiomyopathy. Interrelations of clinical manifestations, pathophysiology, and therapy (1).

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Primary (genetic) cardiomyopathies in infancy. A survey of possible disorders and guidelines for diagnosis

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Cardiomyopathy in the Kearns-Sayre syndrome

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Deficiency of the reduced nicotinamide adenine dinucleotide dehydrogenase component of complex I of mitochondrial electron transport. Fatal infantile lactic acidosis and hypermetabolism with skeletal-cardiac myopathy and encephalopathy

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Oxidative phosphorylation diseases. Disorders of two genomes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

22 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) decrease in diastolic left ventricular function assessed by echocardiography.

25 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

A mitochondrial encephalomyopathy: the first case with an established defect at the level of coenzyme Q.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Mitochondrial encephalomyopathy. A variant with heart failure and liver steatosis.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Cytochrome c oxidase deficiency in Leigh syndrome.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Cytochrome c oxidase deficiency in infancy

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Kearns-Sayre syndrome and dilated cardiomyopathy

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Generalized mitochondrial microangiopathy and vascular cytochrome c oxidase deficiency. Occurrence in a case of MELAS syndrome with mitochondrial cardiomyopathy-myopathy and combined complex I/IV deficiency.

17 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Pleiotropic molecular defects in energy-transducing complexes in mitochondrial encephalomyopathy (MELAS).

20 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1511042

Inherited cardiomyopathies

20 August 2018

1 reference

12 December 2020

Two cases of NADH-coenzyme Q reductase deficiency: relationship to MELAS syndrome

1 reference

12 December 2020

A mitochondrial encephalomyopathy with cardiomyopathy. A case revealing a defect of complex I in the respiratory chain

1 reference

12 December 2020

Congestive heart failure due to mitochondrial cardiomyopathy in Kearns-Sayre syndrome

1 reference

12 December 2020

Foamy myocardial transformation in a child with a disturbed respiratory chain

1 reference

12 December 2020

[Encephalomyelopathy, cardiomyopathy, cataract and changes in the retinal pigment epithelium resulting from a cytochrome c oxidase deficiency]

1 reference

12 December 2020

Mitochondrial myopathy and cardiomyopathy in siblings

1 reference

12 December 2020

Morphometric comparison of mitochondria and myofibrils of cardiomyocytes between hypertrophic and dilated cardiomyopathies

1 reference

12 December 2020

An X-linked recessive cardiomyopathy with abnormal mitochondria

1 reference

12 December 2020

Mitochondrial cardiomyopathy with involvement of skeletal muscles

1 reference

12 December 2020

Histiocytoid Cardiomyopathy of Infancy: Deficiency of Reducible Cytochrome b in Heart Mitochondria

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

1 reference

12 December 2020

Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies

1 reference

12 December 2020

Hypertrophic cardiomyopathy with mitochondrial myopathy. A new phenotype of complex II defect

1 reference

12 December 2020

Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies

1 reference

12 December 2020

Myopathy and fatal cardiopathy due to cytochrome c oxidase deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1136/ADC.72.3.223

1 reference

21 September 2017

1 reference

21 September 2017

1 reference