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Volumn 21, Issue 1, 2014, Pages 186-188
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POLG mutations associated with remitting/relapsing neurological events
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Author keywords
Immunology; Magnetic resonance imaging; Mitochondrial disorders; Multiple sclerosis; Myopathy
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Indexed keywords
MEPREDNISONE;
MITOCHONDRIAL DNA;
ADULT;
ARTICLE;
BLURRED VISION;
CASE REPORT;
CENTRAL SCOTOMA;
CHRONIC AXONAL SENSORY POLYNEUROPATHY;
CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA;
DEMYELINATING DISEASE;
DIPLOPIA;
DISORDERS OF MITOCHONDRIAL FUNCTIONS;
ELECTROMYOGRAM;
EYE PAIN;
FACIAL HYPOESTHESIA;
FEMALE;
GENE;
GENE DELETION;
GENE DOSAGE;
GENE MUTATION;
GENE SEQUENCE;
GENETIC ASSOCIATION;
HETEROZYGOTE;
HUMAN;
HYPESTHESIA;
MIDDLE AGED;
MULTIPLE SCLEROSIS;
MUSCLE BIOPSY;
MYELITIS;
NEUROLOGIC DISEASE;
NUCLEAR MAGNETIC RESONANCE IMAGING;
OPTIC NEURITIS;
OPTICAL COHERENCE TOMOGRAPHY;
POLG GENE;
POLYNEUROPATHY;
PRIORITY JOURNAL;
PTOSIS;
REAL TIME POLYMERASE CHAIN REACTION;
RECURRENT DISEASE;
VISUAL IMPAIRMENT;
IMMUNOLOGY;
MAGNETIC RESONANCE IMAGING;
MITOCHONDRIAL DISORDERS;
MULTIPLE SCLEROSIS;
MYOPATHY;
ADULT;
AGE OF ONSET;
DNA-DIRECTED DNA POLYMERASE;
FEMALE;
HUMANS;
MIDDLE AGED;
MITOCHONDRIAL DISEASES;
MUTATION;
NERVOUS SYSTEM DISEASES;
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EID: 84890562111
PISSN: 09675868
EISSN: 15322653
Source Type: Journal
DOI: 10.1016/j.jocn.2013.03.019 Document Type: Article |
Times cited : (6)
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References (10)
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