TY  - GEN
AU  - Bruun,Cathrine Foyn
AU  - Langbakk,Bodil
AU  - Eriksson Steigen,Sonja
TI  - Purpura fulminans as a sequel to erythema nodosum in a child with homozygous Leiden mutation and acquired protein S deficiency
SN  - 0803-5253
PY  - 2006///0106
KW  - Biopsy, Needle
KW  - Child
KW  - Combined Modality Therapy
KW  - Erythema Nodosum
KW  - complications
KW  - Factor V
KW  - genetics
KW  - Follow-Up Studies
KW  - Heparin
KW  - therapeutic use
KW  - Humans
KW  - IgA Vasculitis
KW  - Immunohistochemistry
KW  - Male
KW  - Plasma Exchange
KW  - Point Mutation
KW  - Prednisolone
KW  - Protein S Deficiency
KW  - Risk Assessment
KW  - Severity of Illness Index
KW  - Treatment Outcome
KW  - Warfarin
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1111/j.1651-2227.2005.tb02063.x
ER  -