Versmold, H T <br/><br/>
A metabolic disorder similar to Zellweger syndrome with hepatic acatalasia and absence of peroxisomes, altered content and redox state of cytochromes, and infantile cirrhosis with hemosiderosis.  [electronic resource] 

 -  European journal of pediatrics  Mar 1977 
 - 261-75 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0340-6199 
<br/><br/><label>Standard No.: </label>10.1007/BF00441934  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Catalase--metabolism<br/>Cytochromes--analysis<br/>Diagnosis, Differential<br/>Endoplasmic Reticulum--ultrastructure<br/>Hemosiderosis--diagnosis<br/>Humans<br/>Infant<br/>Liver--enzymology<br/>Liver Cirrhosis--diagnosis<br/>Male<br/>Metabolism, Inborn Errors--diagnosis<br/>Microbodies--ultrastructure<br/>Microscopy, Electron<br/>Mitochondria, Liver--ultrastructure<br/>Muscle Spasticity--diagnosis<br/>Syndrome