A novel CIAS1 mutation and plasma/cerebrospinal fluid cytokine profile in a German patient with neonatal-onset multisystem inflammatory disease responsive to methotrexate therapy.

Pediatrics

Volumn 114, Issue 1, 2004, Pages

  Stojanov, Silvia ^a   Weiss, Michael ^a   Lohse, Peter ^a   Belohradsky, Bernd H ^a  

^a UNIVERSITY OF MUNICH   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CARRIER PROTEIN; CIAS1 PROTEIN, HUMAN; CYTOKINE; GLUCOCORTICOID; IMMUNOSUPPRESSIVE AGENT; METHOTREXATE;

ARTHRALGIA; ARTICLE; BLOOD; CASE REPORT; CENTRAL NERVOUS SYSTEM DISEASE; CEREBROSPINAL FLUID; CHILD; CHRONIC DISEASE; GENETICS; HUMAN; INFLAMMATION; MALE; MENINGITIS; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; OPTIC NERVE DISEASE; SYNDROME; URTICARIA;

ARTHRALGIA; CARRIER PROTEINS; CENTRAL NERVOUS SYSTEM DISEASES; CHILD; CHRONIC DISEASE; CYTOKINES; DNA MUTATIONAL ANALYSIS; GLUCOCORTICOIDS; HUMANS; IMMUNOSUPPRESSIVE AGENTS; INFLAMMATION; MALE; MENINGITIS; METHOTREXATE; MUTATION, MISSENSE; OPTIC NERVE DISEASES; SYNDROME; URTICARIA;

MLCS; MLOWN;

EID: 4644370590     PISSN: None     EISSN: 10984275     Source Type: Journal    
DOI: 10.1542/peds.114.1.e124     Document Type: Article

References (0)