Hereditary Autoinflammatory Diseases

Known as: Hereditary Recurrent Fevers, Disease, Reimann Periodic, Hereditary Autoinflammation Disease 
Hereditary inflammation conditions, characterized by recurrent episodes of systemic inflammation. Common symptoms include recurrent fever, rash… (More)
National Institutes of Health

Related topics

Related topics

9 relations
Familial Mediterranean FeverIn BloodMicrobiologicalchemically induced
(More)

Narrower (2)

INTERLEUKIN 1 RECEPTOR ANTAGONIST DEFICIENCYTNF receptor-associated periodic fever syndrome (TRAPS)

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2017
Review
2017
The NLRP3 and Pyrin Inflammasomes: Implications in the Pathophysiology of Autoinflammatory Diseases
Inflammasomes are multiprotein complexes that critically control different aspects of innate and adaptive immunity. Among them we… (More)
Is this relevant?
Review
2014
Review
2014
IL-1 blockade in autoinflammatory syndromes.
Monogenic autoinflammatory syndromes present with excessive systemic inflammation including fever, rashes, arthritis, and organ… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Review
2010
Review
2010
IL-1 pathways in inflammation and human diseases
Interleukin (IL)-1 was first cloned in the 1980s, and rapidly emerged as a key player in the regulation of inflammatory processes… (More)
Is this relevant?
Review
2009
Review
2009
Horror autoinflammaticus: the molecular pathophysiology of autoinflammatory disease (*).
The autoinflammatory diseases are characterized by seemingly unprovoked episodes of inflammation, without high-titer… (More)
Is this relevant?
Review
2009
Review
2009
Immunological and inflammatory functions of the interleukin-1 family.
More than any other cytokine family, the interleukin (IL)-1 family is closely linked to the innate immune response. This linkage… (More)
Is this relevant?
Highly Cited
2008
Highly Cited
2008
A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children.
OBJECTIVE To identify a set of clinical parameters that can predict the probability of carrying mutations in one of the genes… (More)
  • table 2
  • table 3
  • table 4
  • figure 1
  • table 5
Is this relevant?
Highly Cited
2008
Highly Cited
2008
Mutations in NALP12 cause hereditary periodic fever syndromes.
NALP proteins, also known as NLRPs, belong to the CATERPILLER protein family involved, like Toll-like receptors, in the… (More)
  • figure 1
  • figure 2
  • figure 3
Is this relevant?
Highly Cited
2008
Highly Cited
2008
The infevers autoinflammatory mutation online registry: update with new genes and functions.
Infevers (Internet Fevers; http://fmf.igh.cnrs.fr/ISSAID/infevers), a website dedicated to mutations responsible for hereditary… (More)
Is this relevant?
Highly Cited
2002
Highly Cited
2002
De novo CIAS1 mutations, cytokine activation, and evidence for genetic heterogeneity in patients with neonatal-onset multisystem inflammatory disease (NOMID): a new member of the expanding family of…
OBJECTIVE Neonatal-onset multisystem inflammatory disease (NOMID; also known as chronic infantile neurologic, cutaneous… (More)
Is this relevant?
Highly Cited
2001
Highly Cited
2001
Familial cold autoinflammatory syndrome: phenotype and genotype of an autosomal dominant periodic fever.
BACKGROUND Familial cold autoinflammatory syndrome (FCAS), commonly known as familial cold urticaria, is a rare autosomal… (More)
Is this relevant?