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6. A Chinese case of Nakajo-Nishimura syndrome with novel compound heterozygous mutations of the PSMB8 gene. Jia T; Zheng Y; Feng C; Yang T; Geng S BMC Med Genet; 2020 Jun; 21(1):126. PubMed ID: 32513120 [TBL] [Abstract][Full Text] [Related]
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12. Myositis with sarcoplasmic inclusions in Nakajo-Nishimura syndrome: a genetic inflammatory myopathy. Ayaki T; Murata K; Kanazawa N; Uruha A; Ohmura K; Sugie K; Kasagi S; Li F; Mori M; Nakajima R; Sasai T; Nishino I; Ueno S; Urushitani M; Furukawa F; Ito H; Takahashi R Neuropathol Appl Neurobiol; 2020 Oct; 46(6):579-587. PubMed ID: 32144790 [TBL] [Abstract][Full Text] [Related]
14. Pluripotent Stem Cell Model of Nakajo-Nishimura Syndrome Untangles Proinflammatory Pathways Mediated by Oxidative Stress. Honda-Ozaki F; Terashima M; Niwa A; Saiki N; Kawasaki Y; Ito H; Hotta A; Nagahashi A; Igura K; Asaka I; Li HL; Yanagimachi M; Furukawa F; Kanazawa N; Nakahata T; Saito MK Stem Cell Reports; 2018 Jun; 10(6):1835-1850. PubMed ID: 29731430 [TBL] [Abstract][Full Text] [Related]
15. Efficacy and safety of baricitinib in Japanese patients with autoinflammatory type I interferonopathies (NNS/CANDLE, SAVI, And AGS). Kanazawa N; Ishii T; Takita Y; Nishikawa A; Nishikomori R Pediatr Rheumatol Online J; 2023 Apr; 21(1):38. PubMed ID: 37087470 [TBL] [Abstract][Full Text] [Related]
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17. CANDLE syndrome: chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature-a rare case with a novel mutation. Cavalcante MP; Brunelli JB; Miranda CC; Novak GV; Malle L; Aikawa NE; Jesus AA; Silva CA Eur J Pediatr; 2016 May; 175(5):735-40. PubMed ID: 26567544 [TBL] [Abstract][Full Text] [Related]
18. Panniculitis: A Cardinal Sign of Autoinflammation. Borges T; Silva S Curr Rheumatol Rev; 2024; 20(4):350-360. PubMed ID: 37921131 [TBL] [Abstract][Full Text] [Related]
19. CANDLE Syndrome As a Paradigm of Proteasome-Related Autoinflammation. Torrelo A Front Immunol; 2017; 8():927. PubMed ID: 28848544 [TBL] [Abstract][Full Text] [Related]
20. Human induced pluripotent stem cells generated from Chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome patients with a homozygous mutation in the PSMB8 gene (NIHTVBi016-A, NIHTVBi017-A, NIHTVBi018-A). Yu Q; Mehta A; Zou J; Beers J; de Jesus Rasheed AA; Goldbach-Mansky R; Boehm M; Chen G Stem Cell Res; 2022 Jul; 62():102820. PubMed ID: 35660921 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]