(Q73764593)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

title

Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

hypertrophic cardiomyopathy

6 November 2019

main subject

1 reference

J Marin-Garcia

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

R Ananthakrishnan

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

M J Goldenthal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

J J Filiano

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

A Perez-Atayde

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

publication date

1 September 1997

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

6 November 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

volume

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

6 November 2019

page(s)

674-680

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9323562%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1023/a:1005322409330

6 November 2019

exact match

0 references

cites work

Prognostic implications of novel beta cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy

1 reference

12 December 2020

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

1 reference

12 December 2020

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

1 reference

12 December 2020

Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome

1 reference

12 December 2020

Endomyocardial biopsies for early detection of mitochondrial disorders in hypertrophic cardiomyopathies

1 reference

12 December 2020

Mitochondrial mutation in fatal infantile cardiomyopathy

1 reference

12 December 2020

OXPHOS defects and mitochondrial DNA mutations in cardiomyopathy

1 reference

12 December 2020

Leigh syndrome and hypertrophic cardiomyopathy in an infant with a mitochondrial DNA point mutation (T8993G).

1 reference

12 December 2020

Dilated cardiomyopathy in a zidovudine-treated AIDS patient

1 reference

12 December 2020

A novel mtDNA point mutation in maternally inherited cardiomyopathy

1 reference

12 December 2020

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

1 reference

12 December 2020

Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

1 reference

12 December 2020

Mitochondrial function in children with idiopathic dilated cardiomyopathy.

1 reference

12 December 2020

mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases

1 reference

12 December 2020

Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial tRNA(Lys) gene (G8363A).

1 reference

12 December 2020

Cardiomyopathy Associated with Antiretroviral Therapy in Patients with HIV Infection: A Report of Six Cases

1 reference

12 December 2020

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

12 December 2020

Specific mitochondrial DNA deletions in idiopathic dilated cardiomyopathy

1 reference

12 December 2020

A novel mitochondrial DNA point mutation associated with mitochondrial encephalocardiomyopathy.

1 reference

12 December 2020

Mitochondrial tRNA(Ile) mutation in fatal cardiomyopathy

1 reference

12 December 2020

Depletion of mitochondrial DNA in the liver of a patient with lactic acidemia and hypoketotic hypoglycemia.

1 reference

12 December 2020

Impaired mitochondrial function in idiopathic dilated cardiomyopathy: biochemical and molecular analysis

1 reference

12 December 2020

Mitochondrial toxicity of antiviral drugs

1 reference

12 December 2020