Tulinius, M H <br/><br/>
Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes.  [electronic resource] 

 -  The Journal of pediatrics  Aug 1991 
 - 251-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0022-3476 
<br/><br/><label>Standard No.: </label>10.1016/s0022-3476(05)80735-8  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Biopsy<br/>Central Nervous System Diseases--diagnosis<br/>Child<br/>Child, Preschool<br/>Chromosome Deletion<br/>DNA, Mitochondrial--genetics<br/>Diagnosis, Differential<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Mitochondria, Muscle--chemistry<br/>Muscles--metabolism<br/>Neuromuscular Diseases--diagnosis<br/>Oximetry<br/>Spectrophotometry<br/>Syndrome