Syndrome of encephalopathy, petechiae, and ethylmalonic aciduria

Pediatric Neurology

Volumn 17, Issue 2, 1997, Pages 165-170

  García Silva, M Teresa ^a,b   Ribes, Antonia ^c   Campos, Yolanda ^b   Garavaglia, Barbara ^d   Arenas, Joaquin ^b  

^a Mitochondrial Diseases Unit   (Spain)

^b HOSPITAL UNIVERSITARIO 12 DE OCTUBRE   (Spain)

^c CSIC   (Spain)

^d DEPARTMENT OF NEUROSURGERY   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ACYL COENZYME A DEHYDROGENASE; CYTOCHROME C OXIDASE; MALONIC ACID;

ACIDURIA; ACROCYANOSIS; ARTICLE; BRAIN DISEASE; CASE REPORT; CHILD; CHRONIC DIARRHEA; FATTY ACID OXIDATION; HISTOCHEMISTRY; HUMAN; MALE; MUSCLE CONTRACTION; MUSCLE HYPOTONIA; NUCLEAR MAGNETIC RESONANCE IMAGING; PETECHIA; PRIORITY JOURNAL; RESPIRATORY CHAIN;

BRAIN; CYTOCHROME-C OXIDASE DEFICIENCY; DNA, MITOCHONDRIAL; HUMANS; INFANT; LEIGH DISEASE; MALE; MALONATES; MUSCLE, SKELETAL; PURPURA;

EID: 0343471867     PISSN: 08878994     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0887-8994(97)00048-9     Document Type: Article

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