Volume 11 Supplement 1
7th Congress of International Society of Systemic Auto-Inflammatory Diseases (ISSAID)
Meeting abstracts
Publication of this supplement has been funded by the International congress on autoinflammatory disease (ISSAID) 2013. Abstracts are based on presentations made at the conference from ISSAID 2013.
7th Congress of International Society of Systemic Auto-Inflammatory Diseases (ISSAID). Go to conference site.
Lausanne, Switzerland22-26 May 2013
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Citation: Pediatric Rheumatology 2013 11(Suppl 1):A101
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OR7-001 – By chip pyrin binds the IRF2 promoter
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A102 -
OR7-002 – Pyrin 577 mutations in dominant autoinflammation
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A103 -
OR7-003 – MEFV genotype, IL1B and role of NLRP3 in FMF
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A104 -
OR7-004 – Validation of AIDAI score
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A105 -
OR7-005 – Canakinumab in childhood colchicine resistant FMF
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A106 -
OR7-006 – Autophagy as a player in inflammation in TRAPS
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A107 -
P02-001 – A novel TNFRSF1A mutation in periodic fever
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A108 -
P02-002 - IL36RN mutations in patients with DITRA
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A109 -
P02-003 - HIDS in a consanguineous family form Saudi Arabia?
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A110 -
P02-004 - AIDs in a registry of children in North America
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A111 -
P02-005 - Overlap of FMF and HIDS in one Arabic family
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A112 -
P02-006 - A novel PSTPIP1 mutation in PAPA syndrome
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A113 -
P02-007 - Childhood autoinflammatory disorders in Qatar
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A114 -
P02-008 - Dramatic response to canakinumab in MKD
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A115 -
P02-009 - Candle syndrome: expanding spectrum
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A116 -
P02-010 - A novel 24 nucleotide deletion in the TNFRSF1A
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A117 -
P02-011 - TRAPS syndrome debuted as systemic JIA
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A118 -
P02-012 - HAIDS in practice of Russian rheumatologist
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A119 -
P02-013 - TH17 cells and regulatory T cells in TRAPS
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A120 -
P02-014 - Consequences of Arginine 92 mutations in TNFR1
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A121 -
P02-015 - A novel MVK mutation in a child with AA amyloid
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A122 -
P02-016 - A novel PSMB8 mutation causing candle syndrome
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A123 -
P02-017 - Periodic fever syndrome masquerading as eczema…
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A124 -
P02-018 - PSTPIP1 gene mutations in periodic fever patients
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A125 -
P02-019 - Detection of risk factors for AA-amyloidosis
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A126 -
P02-020 - CAPS in Turkish children: treatment with ANTI IL1
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A127 -
P02-021 - Atypical CAPS consequence of novel NLPR3 mutations
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A128 -
P02-022 - Atypical cryopirin associated periodic syndrome
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A129 -
P02-023 - NLRP3 mosaicism as a cause of late-onset CAPS
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A130 -
P02-024 - Clinical impact of V198M mutation in NLRP3 gene
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A131 -
P02-025 - Homozygous Q705K sequence variant in NLRP3
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A132 -
P02-026 - Model-based characterization of the PKPD relationship for canakinumab in CAPS: a step towards personalized
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A133 -
P02-027 - Quality of life in CAPS treated by Canakinumab
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A134 -
P02-028 - Muckle-Wells syndrome and renal transplantation
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A135 -
P02-029 - CAPS or SJIA
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A136 -
P02-030 - Unusual CNS manifestation
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A137 -
P02-031 - Phenotype of V198M and Q703K NLRP3 variants
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A138 -
P02-032 - CAPS: a novel mutation and an unusual phenotype
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A139 -
P02-033 - CAPS diagnosis and treatment in an Israeli family
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A140 -
PW02-001 - Exome sequencing for autoinflammatory disorders
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A141 -
PW02-002 - Single MVK mutation and recurrent fevers
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A142 -
PW02-003 - Efficacy of anakinra in etanercept-resistant TRAPS
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A143 -
PW02-004 - Autoinflammatory syndromes: a clinical review
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A144 -
PW02-005 - A web registry of genotype-phenotype correlation
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A145 -
PW02-006 - PAPA syndrome clinical spectrum and IL1B release
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A146 -
PW02-007 - The Eurofever registry: 3 years of enrollment
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A147 -
PW02-008 - TRAPS in the real world: an international registry
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A148 -
PW02-009 - PAPA syndrome: results from the Euroefever registry
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A149 -
PW02-010 - The diagnostic challenge of bone lesions in AID
Citation: Pediatric Rheumatology 2013 11(Suppl 1):A150
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