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Rowczenio, Dorota M.; Pathak, Shelly; Arostegui, Juan I.; Mensa-Vilaro, Anna; Omoyinmi, Ebun; Brogan, Paul; Lipsker, Dan; Scambler, Thomas; Owen, Roger; Trojer, Hadija; Baginska, Anna; Gillmore, Julian D.; Wechalekar, Ashutosh D.; Lane, Thirusha; Williams, Rene; Youngstein, Taryn; Hawkins, Philip N.; Savic, Sinisa; Lachmann, Helen J.

Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome

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  • Media type: E-Article
  • Title: Molecular genetic investigation, clinical features, and response to treatment in 21 patients with Schnitzler syndrome
  • Contributor: Rowczenio, Dorota M.; Pathak, Shelly; Arostegui, Juan I.; Mensa-Vilaro, Anna; Omoyinmi, Ebun; Brogan, Paul; Lipsker, Dan; Scambler, Thomas; Owen, Roger; Trojer, Hadija; Baginska, Anna; Gillmore, Julian D.; Wechalekar, Ashutosh D.; Lane, Thirusha; Williams, Rene; Youngstein, Taryn; Hawkins, Philip N.; Savic, Sinisa; Lachmann, Helen J.
  • Published: American Society of Hematology, 2018
  • Published in: Blood, 131 (2018) 9, Seite 974-981
  • Language: English
  • DOI: 10.1182/blood-2017-10-810366
  • ISSN: 0006-4971; 1528-0020
  • Origination:
  • Footnote:
  • Description: <jats:title>Key Points</jats:title><jats:p>We found no evidence of somatic NLRP3 mosaicism in the pathogenesis of Schnitzler syndrome. Pathogenic inflammasome activation is supported by increased ASC, IL-18, IL-6, and anakinra response.</jats:p>
  • Access State: Open Access