Lundy, C T <br/><br/>
Acute respiratory distress syndrome in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial trifunctional protein deficiencies.  [electronic resource] 

 -  Journal of inherited metabolic disease  2003 
 - 537-41 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0141-8955 
<br/><br/><label>Standard No.: </label>10.1023/a:1025995813914  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>3-Hydroxyacyl CoA Dehydrogenases--deficiency<br/>Anti-Inflammatory Agents--therapeutic use<br/>Female<br/>HELLP Syndrome--complications<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Lipid Metabolism, Inborn Errors--complications<br/>Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase<br/>Lung--pathology<br/>Male<br/>Methylprednisolone--therapeutic use<br/>Mitochondrial Trifunctional Protein<br/>Multienzyme Complexes--deficiency<br/>Pregnancy<br/>Respiratory Distress Syndrome, Newborn--etiology<br/>Respiratory Function Tests