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

To date, the pathogenic mechanisms underlying Schnitzler syndrome remain obscure, in particular, the interplay between the monoclonal protein and increased interleukin-1β (IL-1β) production, although interest in the contribution of genetic factors has been fueled by detection of somatic NLRP3 mosaic...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
में प्रकाशित:Blood
मुख्य लेखकों: 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.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: American Society of Hematology 2018
विषय:
Immunobiology and Immunotherapy
ऑनलाइन पहुंच:https://ncbi.nlm.nih.gov/pmc/articles/PMC5877784/
https://ncbi.nlm.nih.gov/pubmed/29284595
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1182/blood-2017-10-810366
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