Metabolic cardiomyopathy and mitochondrial disorders in the pediatric intensive care unit.

The Journal of pediatrics

Volumn 151, Issue 5, 2007, Pages 538-541

  Kane, Jason M ^a   Rossi, Janet ^a   Tsao, Sabrina ^a   Burton, Barbara K ^a  

^a NORTHWESTERN UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ARTICLE; CARDIOGENIC SHOCK; CARDIOMYOPATHY; CHILD; CLINICAL OBSERVATION; CLINICAL STUDY; DIAGNOSIS; GENE DELETION; GENETICS; HEART BLOCK; HUMAN; INTENSIVE CARE; KEARNS SAYRE SYNDROME; MALE;

CARDIOMYOPATHIES; CHILD; DNA, MITOCHONDRIAL; HEART BLOCK; HUMANS; INTENSIVE CARE UNITS, PEDIATRIC; KEARNS-SAYER SYNDROME; MALE; SEQUENCE DELETION; SHOCK, CARDIOGENIC;

MLCS; MLOWN;

EID: 38449100096     PISSN: None     EISSN: 10976833     Source Type: Journal    
DOI: 10.1016/j.jpeds.2007.05.009     Document Type: Article

References (0)