MELAS syndrome and cardiomyopathy: linking mitochondrial function to heart failure pathogenesis

Selective Elimination of Mitochondrial Mutations in the Germline by Genome Editing

(2015) Pradeep Reddy et al.   CELL

Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseases

(2015) Karim Wahbi et al.   EUROPEAN HEART JOURNAL

Cardiac manifestations of primary mitochondrial disorders

(2014) Josef Finsterer et al.   INTERNATIONAL JOURNAL OF CARDIOLOGY

Cardiotoxicity of doxorubicin is mediated through mitochondrial iron accumulation

(2014) Yoshihiko Ichikawa et al.   JOURNAL OF CLINICAL INVESTIGATION

Detection rates and phenotypic spectrum of m.3243A>G in the MT-TL1 gene: A molecular diagnostic laboratory perspective

(2014) J. Chin et al.   MITOCHONDRION

Divergent Mitochondrial Biogenesis Responses in Human Cardiomyopathy

(2013) Preeti Ahuja et al.   CIRCULATION

2013 ACCF/AHA Guideline for the Management of Heart Failure: Executive Summary

(2013) Clyde W. Yancy et al.   CIRCULATION

Impact of the renin–angiotensin system on cardiac energy metabolism in heart failure

(2013) Jun Mori et al.   JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY

Clinical features of Friedreich's ataxia: classical and atypical phenotypes

(2013) Michael H. Parkinson et al.   JOURNAL OF NEUROCHEMISTRY

The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender?

(2013) Michelangelo Mancuso et al.   JOURNAL OF NEUROLOGY

The UK MRC Mitochondrial Disease Patient Cohort Study: clinical phenotypes associated with the m.3243A>G mutation--implications for diagnosis and management

(2013) V. Nesbitt et al.   JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY

The Heart in Friedreich Ataxia

(2012) Frank Weidemann et al.   CIRCULATION

Mitochondrial A3243G Mutation With Manifestation of Acute Dilated Cardiomyopathy

(2012) Nicolas Stalder et al.   Circulation-Heart Failure

Cardiac involvement in mitochondrial DNA disease: clinical spectrum, diagnosis, and management

(2012) M. G. D. Bates et al.   EUROPEAN HEART JOURNAL

High risk of severe cardiac adverse events in patients with mitochondrial m.3243A>G mutation

(2012) E. Malfatti et al.   NEUROLOGY

Monogenic Mitochondrial Disorders

(2012) Werner J.H. Koopman et al.   NEW ENGLAND JOURNAL OF MEDICINE

Friedreich's ataxia: Pathology, pathogenesis, and molecular genetics

(2011) Arnulf H. Koeppen   JOURNAL OF THE NEUROLOGICAL SCIENCES

MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients

(2011) Paulo José Lorenzoni et al.   MITOCHONDRION

Genotype–phenotype correlations in Leber hereditary optic neuropathy

(2010) Katarzyna Tońska et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Factors Associated With Pulseless Electric Activity Versus Ventricular Fibrillation

(2010) Carmen Teodorescu et al.   CIRCULATION

Myc controls transcriptional regulation of cardiac metabolism and mitochondrial biogenesis in response to pathological stress in mice

(2010) Preeti Ahuja et al.   JOURNAL OF CLINICAL INVESTIGATION

Polymerase Gamma 1 Mutations

(2010) Margherita Milone et al.   NEUROLOGIST

Cardiac involvement is frequent in patients with the m.8344A>G mutation of mitochondrial DNA

(2010) K. Wahbi et al.   NEUROLOGY

Eplerenone in Patients with Systolic Heart Failure and Mild Symptoms

(2010) Faiez Zannad et al.   NEW ENGLAND JOURNAL OF MEDICINE

Mitochondrial Encephalopathy, Lactic Acidosis, and Strokelike Episodes

(2009) Douglas M. Sproule et al.   Annals of the New York Academy of Sciences

Accumulation of oxidative stress around the stroke-like lesions of MELAS patients

(2009) Yuri Katayama et al.   MITOCHONDRION

Pathogenic Mitochondrial DNA Mutations Are Common in the General Population

(2008) Hannah R. Elliott et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Resistance training in patients with single, large-scale deletions of mitochondrial DNA

(2008) J. L. Murphy et al.   BRAIN

A Mitochondrial Protein Compendium Elucidates Complex I Disease Biology

(2008) David J. Pagliarini et al.   CELL

Conserved Metabolic Regulatory Functions of Sirtuins

(2008) Bjoern Schwer et al.   Cell Metabolism

Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation

(2008) R. Murphy et al.   DIABETIC MEDICINE

Mitochondrial centrality in heart failure

(2008) José Marín-García et al.   HEART FAILURE REVIEWS

ACC/AHA/HRS 2008 Guidelines for Device-Based Therapy of Cardiac Rhythm Abnormalities

(2008) Andrew E. Epstein et al.   JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY

Leigh and Leigh-Like Syndrome in Children and Adults

(2008) Josef Finsterer   PEDIATRIC NEUROLOGY