Diagnostic approach to mitochondrial disorders: The need for a reliable biomarker

Current Molecular Medicine

Volumn 9, Issue 9, 2009, Pages 1095-1107

  Mancuso, M ^a   Orsucci, D ^a   Coppede F ^a   Nesti, C ^a   Choub, A ^a   Siciliano, G ^a  

^a UNIVERSITY OF PISA   (Italy)

Author keywords

CoQ10; Exercise; Lactate; Mitochondria; mtDNA; Myopathy; Oxidative stress; Respiratory chain

Indexed keywords

CREATINE KINASE; FUMARIC ACID; LACTIC ACID; MALIC ACID; MITOCHONDRIAL DNA; UBIDECARENONE;

CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; CLINICAL FEATURE; COMPLEX II DEFICIENCY; CREATINE KINASE BLOOD LEVEL; DIAGNOSTIC VALUE; DIFFERENTIAL DIAGNOSIS; DISEASE CLASSIFICATION; DISEASE MARKER; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTROMYOGRAPHY; EXERCISE TEST; GENE MUTATION; GENETIC ANALYSIS; HUMAN; KEARNS SAYRE SYNDROME; LACTATE BLOOD LEVEL; LEBER HEREDITARY OPTIC NEUROPATHY; LEIGH DISEASE; MELAS SYNDROME; MERRF SYNDROME; MITOCHONDRIAL DNA DEPLETION SYNDROME; MITOCHONDRIAL DNA DISORDER; MNGIE SYNDROME; MUSCLE BIOPSY; NARP SYNDROME; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PEARSON SYNDROME; PREVALENCE; PROTEIN EXPRESSION; PYRUVATE DEHYDROGENASE COMPLEX DEFICIENCY; RELIABILITY; RESPIRATORY CHAIN; REVIEW; SINGLE PHOTON EMISSION COMPUTER TOMOGRAPHY; SUPPLEMENTATION;

BIOLOGICAL MARKERS; HUMANS; MITOCHONDRIAL DISEASES; REPRODUCIBILITY OF RESULTS;

EID: 73249119723     PISSN: 15665240     EISSN: None     Source Type: Journal    
DOI: 10.2174/156652409789839099     Document Type: Review

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