Primary complement and antibody deficiencies in autoimmune rheumatologic diseases with juvenile onset: A prospective study at two centers

Pediatric Rheumatology

Volumn 13, Issue 1, 2015, Pages

  Spârchez, Mihaela ^a,c   Lupan, Iulia ^b   Delean, Dan ^c   Bizo, Aurel ^a,c   Damian, Laura ^d   Muntean, Laura ^a,d   Tămaş, Maria Magdalena ^a,d   Bolba, Claudia ^c   Simionescu, Bianca ^a,c   Slăvescu, Cristina ^a,c   Felea, Ioana ^d   Lazăr, Călin ^c   Spârchez, Zeno ^a   Rednic, Simona ^a,d  

^a IULIU HATIEGANU UNIVERSITY OF MEDICINE AND PHARMACY   (Romania)

^b BABE BOLYAI UNIVERSITY   (Romania)

^c Emergency Hospital for Children   (Romania)

^d Spitalul Clinic Judetean de Urgenta Cluj   (Romania)

Author keywords

Antibody deficiency; Juvenile idiopathic arthritis; Juvenile onset systemic lupus erythematosus; Primary complement

Indexed keywords

COMPLEMENT COMPONENT C2; COMPLEMENT COMPONENT C4; IMMUNOGLOBULIN A; COMPLEMENT;

ADOLESCENT; ADULT; ALLOTYPE; ARTICLE; AUTOIMMUNE HEPATITIS; CHILD; COHORT ANALYSIS; COMPLEMENT DEFICIENCY; DISEASE ACTIVITY; DISEASE COURSE; FEMALE; GENETIC SCREENING; HOSPITAL PATIENT; HUMAN; HUMORAL IMMUNE DEFICIENCY; IDIOPATHIC DISEASE; IMMUNE DEFICIENCY; IMMUNOGLOBULIN A DEFICIENCY; IMMUNOGLOBULIN BLOOD LEVEL; IMMUNOGLOBULIN DEFICIENCY; JUVENILE; JUVENILE RHEUMATOID ARTHRITIS; MAJOR CLINICAL STUDY; MALE; MEDICAL CARE; MIXED CONNECTIVE TISSUE DISEASE; OBSERVATIONAL STUDY; ONSET AGE; PRESCHOOL CHILD; PREVALENCE; PRIORITY JOURNAL; PROSPECTIVE STUDY; RETROSPECTIVE STUDY; RHEUMATIC DISEASE; SCHOOL CHILD; SCLERODERMA; SCLERODERMA OVERLAP SYNDROME; SYNDROME; SYSTEMIC LUPUS ERYTHEMATOSUS; SYSTEMIC VASCULITIS; TERTIARY CARE CENTER; UVEITIS; ARTHRITIS, JUVENILE; AUTOIMMUNE DISEASES; CLINICAL TRIAL; DEFICIENCY; IMMUNOLOGIC DEFICIENCY SYNDROMES; IMMUNOLOGY; INFANT; LUPUS ERYTHEMATOSUS, SYSTEMIC; MULTICENTER STUDY; RHEUMATIC DISEASES; SCLERODERMA, SYSTEMIC;

ADOLESCENT; AGE OF ONSET; ARTHRITIS, JUVENILE; AUTOIMMUNE DISEASES; CHILD; CHILD, PRESCHOOL; COMPLEMENT C2; COMPLEMENT C4; COMPLEMENT SYSTEM PROTEINS; FEMALE; HUMANS; IMMUNOLOGIC DEFICIENCY SYNDROMES; INFANT; LUPUS ERYTHEMATOSUS, SYSTEMIC; MALE; PROSPECTIVE STUDIES; RHEUMATIC DISEASES; SCLERODERMA, SYSTEMIC; SYSTEMIC VASCULITIS; UVEITIS;

EID: 84959126898     PISSN: None     EISSN: 15460096     Source Type: Journal    
DOI: 10.1186/s12969-015-0050-8     Document Type: Article

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