S100A12 as diagnostic tool in the differential diagnosis of sJIA associated MAS vs. hereditary or acquired HLH

Pediatric Rheumatology

Volumn 13, Issue 1, 2015, Pages

  Holzinger, D ^a   Fall, N ^b   Grom, A ^b   de Jager, W ^c   Vastert, S ^c   Strippoli, R ^d   Bracaglia, C ^e   Sundberg, E ^f   Horne, A ^f   Ehl, S ^g   De Benedetti, F ^e   Beutel, K ^h   Foell, D ^a  

^a UNIVERSITY HOSPITAL MÜNSTER   (Germany)

^b CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

^c UNIVERSITY MEDICAL CENTER UTRECHT   (Netherlands)

^d SAPIENZA UNIVERSITY OF ROME   (Italy)

^e BAMBINO GESÙ CHILDREN S HOSPITAL   (Italy)

^f KAROLINSKA UNIVERSITY HOSPITAL   (Sweden)

^g UNIVERSITY OF FREIBURG   (Germany)

^h TECHNICAL UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CALGRANULIN C;

ARTICLE; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; DISEASE ACTIVITY; DISEASE ASSOCIATION; HEMOPHAGOCYTIC SYNDROME; HUMAN; MACROPHAGE ACTIVATION SYNDROME; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN DETERMINATION; SYSTEMIC JUVENILE IDIOPATHIC ARTHRITIS;

EID: 84956846830     PISSN: None     EISSN: 15460096     Source Type: Journal    
DOI: 10.1186/1546-0096-13-S1-O64     Document Type: Article

References (0)