These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
144 related articles for article (PubMed ID: 37548074)
1. Subdural hemorrhage, macrocephaly, rash, and developmental delay in an infant: A pathogenic variant in NLRP3 causes CINCA/NOMID. Koti AS; Lanis A; Finlayson S; Canny S; Feldman EA; Miller DE; Rosenwasser N; Scott AA; Wong SC; Feldman KW Am J Med Genet A; 2023 Dec; 191(12):2825-2830. PubMed ID: 37548074 [TBL] [Abstract][Full Text] [Related]
2. A somatic NLRP3 mutation as a cause of a sporadic case of chronic infantile neurologic, cutaneous, articular syndrome/neonatal-onset multisystem inflammatory disease: Novel evidence of the role of low-level mosaicism as the pathophysiologic mechanism underlying mendelian inherited diseases. Aróstegui JI; Lopez Saldaña MD; Pascal M; Clemente D; Aymerich M; Balaguer F; Goel A; Fournier del Castillo C; Rius J; Plaza S; López Robledillo JC; Juan M; Ibañez M; Yagüe J Arthritis Rheum; 2010 Apr; 62(4):1158-66. PubMed ID: 20131270 [TBL] [Abstract][Full Text] [Related]
3. Current status of understanding the pathogenesis and management of patients with NOMID/CINCA. Goldbach-Mansky R Curr Rheumatol Rep; 2011 Apr; 13(2):123-31. PubMed ID: 21538043 [TBL] [Abstract][Full Text] [Related]
4. Necrotizing Funisitis as an Intrauterine manifestation of Cryopyrin-Associated Periodic Syndrome: a case report and review of the literature. Yokoi K; Minamiguchi S; Honda Y; Kobayashi M; Kobayashi S; Nishikomori R Pediatr Rheumatol Online J; 2021 May; 19(1):77. PubMed ID: 34059097 [TBL] [Abstract][Full Text] [Related]
5. High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study. Tanaka N; Izawa K; Saito MK; Sakuma M; Oshima K; Ohara O; Nishikomori R; Morimoto T; Kambe N; Goldbach-Mansky R; Aksentijevich I; de Saint Basile G; Neven B; van Gijn M; Frenkel J; Aróstegui JI; Yagüe J; Merino R; Ibañez M; Pontillo A; Takada H; Imagawa T; Kawai T; Yasumi T; Nakahata T; Heike T Arthritis Rheum; 2011 Nov; 63(11):3625-32. PubMed ID: 21702021 [TBL] [Abstract][Full Text] [Related]
6. Detection of a novel mutation in NLRP3/CIAS1 gene in an Indian child with Neonatal-Onset Multisystem Inflammatory Disease (NOMID). Nair SB; Chavan PP; Athalye AS; Aksentijevich I; Khubchandani RP Clin Rheumatol; 2019 Feb; 38(2):403-406. PubMed ID: 30066283 [TBL] [Abstract][Full Text] [Related]
7. Chronic Infantile Neurological Cutaneous and Articular (CINCA) syndrome: a review. Finetti M; Omenetti A; Federici S; Caorsi R; Gattorno M Orphanet J Rare Dis; 2016 Dec; 11(1):167. PubMed ID: 27927236 [TBL] [Abstract][Full Text] [Related]
8. 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 pyrin-associated autoinflammatory diseases. Aksentijevich I; Nowak M; Mallah M; Chae JJ; Watford WT; Hofmann SR; Stein L; Russo R; Goldsmith D; Dent P; Rosenberg HF; Austin F; Remmers EF; Balow JE; Rosenzweig S; Komarow H; Shoham NG; Wood G; Jones J; Mangra N; Carrero H; Adams BS; Moore TL; Schikler K; Hoffman H; Lovell DJ; Lipnick R; Barron K; O'Shea JJ; Kastner DL; Goldbach-Mansky R Arthritis Rheum; 2002 Dec; 46(12):3340-8. PubMed ID: 12483741 [TBL] [Abstract][Full Text] [Related]
10. Clinical characteristics of Chinese neonates with neonatal-onset multisystem inflammatory disease: a case report and literature review. Zhao C; Liu C; Li X Front Immunol; 2023; 14():1291345. PubMed ID: 38250066 [TBL] [Abstract][Full Text] [Related]
11. Neonatal treatment of CINCA syndrome. Paccaud Y; Berthet G; Von Scheven-Gête A; Vaudaux B; Mivelaz Y; Hofer M; Roth-Kleiner M Pediatr Rheumatol Online J; 2014; 12():52. PubMed ID: 25584041 [TBL] [Abstract][Full Text] [Related]
13. Successful management of cryopyrin-associated periodic syndrome with canakinumab in infancy. Kanariou M; Tantou S; Varela I; Raptaki M; Petropoulou C; Nikas I; Valari M Pediatrics; 2014 Nov; 134(5):e1468-73. PubMed ID: 25349319 [TBL] [Abstract][Full Text] [Related]
14. Diagnosis of cryopyrin-associated periodic syndrome: challenges, recommendations and emerging concepts. Sarrabay G; Grandemange S; Touitou I Expert Rev Clin Immunol; 2015; 11(7):827-35. PubMed ID: 25979514 [TBL] [Abstract][Full Text] [Related]
15. Initial clinical presentation of children with acute and chronic versus acute subdural hemorrhage resulting from abusive head trauma. Feldman KW; Sugar NF; Browd SR J Neurosurg Pediatr; 2015 Aug; 16(2):177-85. PubMed ID: 25932780 [TBL] [Abstract][Full Text] [Related]
16. [Genetics of cryopyrin-associated periodic syndrome]. Kümmerle-Deschner JB; Lohse P Z Rheumatol; 2017 May; 76(4):313-321. PubMed ID: 28197772 [TBL] [Abstract][Full Text] [Related]
17. Case Report: Infantile Urticaria as a Herald of Neonatal Onset Multisystem Inflammatory Disease With a Novel Mutation in NLRP3. Patrick AE; Lyons EM; Ishii L; Boyd AS; Choi JM; Dewan AK; Markle JG Front Immunol; 2021; 12():775140. PubMed ID: 34868041 [TBL] [Abstract][Full Text] [Related]
18. Computational Modeling of NLRP3 Identifies Enhanced ATP Binding and Multimerization in Cryopyrin-Associated Periodic Syndromes. Samson JM; Ravindran Menon D; Vaddi PK; Kalani Williams N; Domenico J; Zhai Z; Backos DS; Fujita M Front Immunol; 2020; 11():584364. PubMed ID: 33329557 [TBL] [Abstract][Full Text] [Related]
19. Clinical and Genetic Spectrum of Nine Cases of NLRP3-Associated Autoinflammatory Disease (NLRP3-AID) and Identification of One Novel NLRP3 Mutation by Genetic Variation Analyses. Shangguan Y; Ding X; Ma L; Cai YX; Xiang S; Huang XF; Shen Y; Yu HG; Zheng W J Immunol Res; 2024; 2024():5722548. PubMed ID: 38481988 [TBL] [Abstract][Full Text] [Related]
20. [Cutaneous neutrophils infiltrates. Case 8. CINCA/NOMID syndrome]. Fraitag S Ann Pathol; 2011 Jun; 31(3):203-7. PubMed ID: 21737003 [No Abstract] [Full Text] [Related] [Next] [New Search]