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autosomal dominant familial Periodic fever

Also Known As:
Periodic fever, familial, autosomal dominant; Familial Hibernian fever; Hibernian fever, familial; TNF receptor-associated periodic syndrome; Tumor necrosis factor receptor-associated periodic syndrome
Networked: 155 relevant articles (5 outcomes, 5 trials/studies)

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Bio-Agent Context: Research Results

Experts

1. Cantarini, Luca: 13 articles (09/2015 - 07/2011)
2. Gattorno, Marco: 10 articles (10/2015 - 10/2009)
3. Rigante, Donato: 10 articles (08/2015 - 08/2009)
4. Frenkel, Joost: 6 articles (09/2015 - 09/2003)
5. Lucherini, Orso Maria: 6 articles (01/2013 - 07/2012)
6. Galeazzi, Mauro: 6 articles (01/2013 - 07/2012)
7. Simon, Anna: 5 articles (09/2015 - 01/2007)
8. Frediani, Bruno: 5 articles (07/2015 - 07/2012)
9. Cimaz, Rolando: 5 articles (01/2013 - 10/2008)
10. Galeazzi, M: 5 articles (07/2011 - 01/2006)

Related Diseases

1. Cryopyrin-Associated Periodic Syndromes
2. Familial Mediterranean Fever (Periodic Disease)
3. Mevalonate Kinase Deficiency
4. Fever (Fevers)
5. Juvenile Rheumatoid Arthritis (Juvenile Idiopathic Arthritis)
09/01/2006 - "We report two cases of tumor necrosis factor receptor-associated periodic syndrome (TRAPS) in patients in whom systemic juvenile idiopathic arthritis (JIA) had initially been diagnosed or suspected. "
09/01/2006 - "Tumor necrosis factor receptor-associated periodic syndrome mimicking systemic juvenile idiopathic arthritis."
10/01/2015 - "Patients with common complex multifactorial diseases such as systemic-onset juvenile idiopathic arthritis (sJIA), and particularly those with rare monogenic autoinflammatory diseases such as cryopyrin-associated periodic syndromes (CAPS) or TNF receptor-associated periodic syndrome (TRAPS), benefited from a deeper understanding of the pathophysiological mechanisms and new treatment options emerging from preclinical studies. "
04/01/2003 - "The differential diagnosis includes other diseases characterized by periodic fevers, such as familial Mediterranean fever, familial Hibernian fever, hyperglobulinemia D syndrome, Behçet's disease, cyclic neutropenia, juvenile rheumatoid arthritis, and several infectious diseases. "
08/01/2009 - "Among the pediatric conditions belonging to this group we can consider hereditary recurrent fevers (familial Mediterranean fever, mevalonate kinase deficiency syndrome, tumor necrosis factor receptor-associated periodic syndrome, cryopyrin-associated periodic syndromes), pyogenic disorders (PAPA syndrome, CRMO syndrome, Majeed syndrome), immune-mediated granulomatous diseases (Blau syndrome, Crohn's disease), and idiopathic febrile syndromes (systemic-onset juvenile idiopathic arthritis, PFAPA syndrome, Behçet syndrome). "

Related Drugs and Biologics

1. Interleukin-1 (Interleukin 1)
2. TNFR-Fc fusion protein (etanercept)
3. Interleukin-1beta (Interleukin 1 beta)
4. Prostaglandins A (PGA)
5. Tumor Necrosis Factor Receptors (Tumor Necrosis Factor Receptor)
6. Tumor Necrosis Factor-alpha (Tumor Necrosis Factor)
7. Synovitis granulomatous with uveitis and cranial neuropathies
8. Immunoglobulin D (IgD)
9. Type I Tumor Necrosis Factor Receptors
10. Pyogenic arthritis, pyoderma gangrenosum, and acne