Bruun, Cathrine Foyn <br/><br/>
Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency.  [electronic resource] 

 -  Acta paediatrica (Oslo, Norway : 1992)  Aug 2005 
 - 1155-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>0803-5253 
<br/><br/><label>Standard No.: </label>10.1111/j.1651-2227.2005.tb02063.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Biopsy, Needle<br/>Child<br/>Combined Modality Therapy<br/>Erythema Nodosum--complications<br/>Factor V--genetics<br/>Follow-Up Studies<br/>Heparin--therapeutic use<br/>Humans<br/>IgA Vasculitis--complications<br/>Immunohistochemistry<br/>Male<br/>Plasma Exchange<br/>Point Mutation<br/>Prednisolone--therapeutic use<br/>Protein S Deficiency--complications<br/>Risk Assessment<br/>Severity of Illness Index<br/>Treatment Outcome<br/>Warfarin--therapeutic use