Investigation of children for mitochondriopathy confirms need for strict patient selection, improved morphological criteria, and better laboratory methods

Human Pathology

Volumn 37, Issue 2, 2006, Pages 173-184

  Miles, Lili ^a   Wong, Brenda L ^a   Dinopoulos, Argirios ^a   Morehart, Paula J ^a   Hofmann, Irene A ^a   Bove, Kevin E ^a  

^a UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

Author keywords

Children; Electron microscopy; Electron transport complex; Histochemistry; Mitochondriopathy; Muscle biopsy

Indexed keywords

CITRATE SYNTHASE; SUCCINATE DEHYDROGENASE;

ADOLESCENT; ADULT; ARTICLE; BRAIN DISEASE; CHILD; CONTROLLED STUDY; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ELECTRON MICROSCOPY; ELECTRON TRANSPORT; ENCEPHALOMYOPATHY; ENERGY METABOLISM; ENZYME ACTIVITY; FEMALE; HISTOCHEMISTRY; HUMAN; INFANT; MAJOR CLINICAL STUDY; MALE; MUSCLE BIOPSY; NEWBORN; PATIENT SELECTION;

ADOLESCENT; ADULT; BIOPSY; CHILD; CHILD, PRESCHOOL; ENERGY METABOLISM; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MITOCHONDRIA, MUSCLE; MITOCHONDRIAL MYOPATHIES; MUSCLES; PATIENT SELECTION;

EID: 30744467678     PISSN: 00468177     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.humpath.2005.10.008     Document Type: Article

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