Reflex sympathetic dystrophy: Complex regional pain syndrome type I in children with mitochondrial disease and maternal inheritance

Archives of Disease in Childhood

Volumn 93, Issue 5, 2008, Pages 390-397

  Higashimoto, T ^a,b,c   Baldwin, E E ^a,d   Gold, J I ^a,b   Boles, R G ^a,b  

^a CHILDREN S HOSPITAL LOS ANGELES   (United States)

^b UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^c CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMITRIPTYLINE; CAFFEINE; CITALOPRAM; DNA; PROPRANOLOL; SERTRALINE; VENLAFAXINE; MITOCHONDRIAL DNA;

ADOLESCENT; BEDTIME DOSAGE; CHEMICAL ANALYSIS; CHILD; COMPLEX REGIONAL PAIN SYNDROME TYPE I; CONTROLLED STUDY; DEPRESSION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; DNA SEQUENCE; DYSAUTONOMIA; EXTRACHROMOSOMAL INHERITANCE; FATIGUE; FEMALE; GASTROINTESTINAL MOTILITY DISORDER; GENETIC VARIABILITY; HEADACHE; HUMAN; LIMB PAIN; MAJOR CLINICAL STUDY; MALE; MEDICAL RECORD REVIEW; MIGRAINE; MUSCLE CRAMP; NECK PAIN; PHYSIOTHERAPY; PRIORITY JOURNAL; REVIEW; TERTIARY HEALTH CARE; VOMITING; ARTICLE; AUTONOMIC NEUROPATHY; CASE CONTROL STUDY; GENETICS; INFANT; NEWBORN; PRESCHOOL CHILD; RETROSPECTIVE STUDY;

ADOLESCENT; AUTONOMIC NERVOUS SYSTEM DISEASES; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; EXTRACHROMOSOMAL INHERITANCE; FEMALE; HUMANS; INFANT; INFANT, NEWBORN; MALE; MITOCHONDRIAL DISEASES; REFLEX SYMPATHETIC DYSTROPHY; RETROSPECTIVE STUDIES;

EID: 44349086358     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/adc.2007.123661     Document Type: Review

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