Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course. - Wikidata - awgldk - TriplyDB

Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.

Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.

http://www.wikidata.org/entity/Q37970121

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Late-onset Mitochondrial Cardiomyopathy Triggered by Anticancer Treatment Mitochondrial cardiomyopathy: pathophysiology, diagnosis, and management.Mitochondrial Mutations in Cardiac Disorders.Quantification of mitochondrial DNA copy number in suspected cancer patients by a well optimized ddPCR method.Mitochondrial Dysfunction and Chronic Disease: Treatment With Natural Supplements.The aetiology of cardiovascular disease: a role for mitochondrial DNA?Methylene blue rescues heart defects in a Drosophila model of Friedreich's ataxia.Management of Bradyarrhythmias in Heart Failure: A Tailored Approach.Hypertrophic cardiomyopathy in mitochondrial disorders: description of an uncommon clinical case.

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Mitochondrial diseases and the heart: an overview of molecular basis, diagnosis, treatment and clinical course.

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Future Cardiology

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Daniele Masarone

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Perry M Elliott

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Raffaella D'Alessandro

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P2860

Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

Mitochondrial DNA mutations in human disease

Sequence and organization of the human mitochondrial genome

Mitochondrial disorders in the nervous system

Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy

Severe infantile hypotonia with ethylmalonic aciduria: case report

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

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10.2217/FCA.11.79

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1

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Giuseppe Limongelli

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2012-01-01T00:00:00Z

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51903550

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22185447

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