Zobrazeno 1 - 10
of 1 976
pro vyhledávání: '"Autoinflammatory disease"'
Autor:
Çağrı Coşkun, Şule Ünal
Publikováno v:
Turkish Journal of Hematology, Vol 41, Iss 3, Pp 133-140 (2024)
Adenosine deaminase 2 (ADA2) deficiency is an autosomal recessively inherited autoinflammatory disorder caused by loss-of-function mutations in the ADA2 gene. Although the pathogenesis involves the triggering of a proinflammatory cascade due to incre
Externí odkaz:
https://doaj.org/article/72e213619c734701b6b135de1eb87be9
Autor:
Osorio‐Aragón I. Yolanda, Milián‐Solís Ximena, Berumen‐Glinz Cristina, Vargas C. Estefanía, Vega‐Memije M. Elisa, Andrade‐Rojas J. Jose, Contreras‐Solis M. Fernanda, González‐Hernández Isaac
Publikováno v:
JEADV Clinical Practice, Vol 3, Iss 2, Pp 710-713 (2024)
Abstract We present the case of a 26‐year‐old female with chronic urticaria (CU) with systemic symptoms in whom comprehensive laboratory and imaging studies led to the diagnosis of idiopathic multicentric Castleman disease. Treatment with rituxim
Externí odkaz:
https://doaj.org/article/01ded831b9534df688ed0b0e044d3bd9
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
Externí odkaz:
https://doaj.org/article/73310f1e4a3d409cae1c07316bb9b291
Autor:
Hafsa Nomani, Song Wu, Ashmia Saif, Frank Hwang, Jane Metzger, Brianne Navetta-Modrov, Peter D. Gorevic, Ivona Aksentijevich, Qingping Yao
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
ObjectiveYao syndrome (YAOS) is formerly called nucleotide-binding oligomerization domain containing 2 (NOD2)-associated autoinflammatory disease.We report a large cohort of YAOS.MethodsWe conducted a retrospective analysis of a cohort of adult patie
Externí odkaz:
https://doaj.org/article/f18c5b5a610241848ecfefd56bdcedc4
Autor:
Steven R. Feldman, MD, PhD, Ran Gao, MS, Rhonda L. Bohn, ScD, Stephani Gray, MPH, Sabrina E. Walton, MSPH, Anouk Déruaz-Luyet, PhD, MPH, Jashin J. Wu, MD
Publikováno v:
JAAD International, Vol 15, Iss , Pp 59-61 (2024)
Externí odkaz:
https://doaj.org/article/186d9dc60dab4149bcaeca83157689fe
Publikováno v:
Indian Pediatrics Case Reports, Vol 4, Iss 2, Pp 106-109 (2024)
Background: Blau syndrome is a monogenic disease resulting from mutations in nucleotide oligomerization domain 2 (NOD2) and is phenotypically characterized by a triad of dermatitis, arthritis, and uveitis. We report Blau syndrome in a child who had b
Externí odkaz:
https://doaj.org/article/fcfff6398c8e4f48aeed404ac41ac5f2
Publikováno v:
Journal of Pharmacy and Bioallied Sciences, Vol 16, Iss 6, Pp 1110-1119 (2024)
Inflammatory chemicals are released by the immune system in response to any perceived danger, including irritants and pathogenic organisms. The caspase activation and the response of inflammation are governed by inflammasomes, which are sensors and t
Externí odkaz:
https://doaj.org/article/7827569ce8f34145b0b5fbb29f415996
Autor:
Guilherme Diogo Silva, João Vitor Mahler, Sérgio Roberto Pereira da Silva Junior, Leonardo Oliveira Mendonça, Pedro Lucas Grangeiro de Sá Barreto Lima, Paulo Ribeiro Nóbrega, Fernando Kok, Fernando Freua
Publikováno v:
BMC Neurology, Vol 24, Iss 1, Pp 1-7 (2024)
Abstract Background Monogenic autoinflammatory disorders result in a diverse range of neurological symptoms in adults, often leading to diagnostic delays. Despite the significance of early detection for effective treatment, the neurological manifesta
Externí odkaz:
https://doaj.org/article/10e5297799cc4e468a769967b8fce8f8
Publikováno v:
Brain, Behavior, & Immunity - Health, Vol 42, Iss , Pp 100906- (2024)
Autoinflammatory diseases (AID) are rare systemic inflammatory disorders due to monogenic or polygenic dysfunction of innate immunity. They affect many organs including the brain and the skin. The spectrum of these diseases has been rapidly expanding
Externí odkaz:
https://doaj.org/article/666955cf92e8455f8e028858e15d40e9
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