162 related articles for article (PubMed ID: 29259686)
1. Dysfunctional immunoproteasomes in autoinflammatory diseases.
Arimochi H; Sasaki Y; Kitamura A; Yasutomo K
Inflamm Regen; 2016; 36():13. PubMed ID: 29259686
[TBL] [Abstract][Full Text] [Related]
2. Nakajo-Nishimura syndrome and related proteasome-associated autoinflammatory syndromes.
Ohmura K
J Inflamm Res; 2019; 12():259-265. PubMed ID: 31576159
[TBL] [Abstract][Full Text] [Related]
3. Proteasome-associated autoinflammatory syndromes: advances in pathogeneses, clinical presentations, diagnosis, and management.
McDermott A; Jacks J; Kessler M; Emanuel PD; Gao L
Int J Dermatol; 2015 Feb; 54(2):121-9. PubMed ID: 25521013
[TBL] [Abstract][Full Text] [Related]
4. Dysregulation of immunoproteasomes in autoinflammatory syndromes.
Yasutomo K
Int Immunol; 2019 Sep; 31(10):631-637. PubMed ID: 30169676
[TBL] [Abstract][Full Text] [Related]
5. Mutations in proteasome subunit β type 8 cause chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature with evidence of genetic and phenotypic heterogeneity.
Liu Y; Ramot Y; Torrelo A; Paller AS; Si N; Babay S; Kim PW; Sheikh A; Lee CC; Chen Y; Vera A; Zhang X; Goldbach-Mansky R; Zlotogorski A
Arthritis Rheum; 2012 Mar; 64(3):895-907. PubMed ID: 21953331
[TBL] [Abstract][Full Text] [Related]
6. PSMB8 encoding the β5i proteasome subunit is mutated in joint contractures, muscle atrophy, microcytic anemia, and panniculitis-induced lipodystrophy syndrome.
Agarwal AK; Xing C; DeMartino GN; Mizrachi D; Hernandez MD; Sousa AB; Martínez de Villarreal L; dos Santos HG; Garg A
Am J Hum Genet; 2010 Dec; 87(6):866-72. PubMed ID: 21129723
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Nakajo-Nishimura syndrome: an autoinflammatory disorder showing pernio-like rashes and progressive partial lipodystrophy.
Kanazawa N
Allergol Int; 2012 Jun; 61(2):197-206. PubMed ID: 22441638
[TBL] [Abstract][Full Text] [Related]
9. An autosomal recessive syndrome of joint contractures, muscular atrophy, microcytic anemia, and panniculitis-associated lipodystrophy.
Garg A; Hernandez MD; Sousa AB; Subramanyam L; Martínez de Villarreal L; dos Santos HG; Barboza O
J Clin Endocrinol Metab; 2010 Sep; 95(9):E58-63. PubMed ID: 20534754
[TBL] [Abstract][Full Text] [Related]
10. Successful treatment of chronic atypical neutrophilic dermatosis with lipodystrophy and elevated temperature (CANDLE) syndrome with tofacitinib.
Patel PN; Hunt R; Pettigrew ZJ; Shirley JB; Vogel TP; de Guzman MM
Pediatr Dermatol; 2021 Mar; 38(2):528-529. PubMed ID: 33512037
[TBL] [Abstract][Full Text] [Related]
11. Induced pluripotent stem cells representing Nakajo-Nishimura syndrome.
Kanazawa N; Honda-Ozaki F; Saito MK
Inflamm Regen; 2019; 39():11. PubMed ID: 31143302
[TBL] [Abstract][Full Text] [Related]
12. Nakajo-Nishimura Syndrome: The First African Case.
Ghodbane NE; Mecibah A; Merzougui Z; Zerguine H; Akakba Z; Slimani S
Mediterr J Rheumatol; 2023 Jun; 34(2):262-265. PubMed ID: 37654638
[TBL] [Abstract][Full Text] [Related]
13. CANDLE Syndrome As a Paradigm of Proteasome-Related Autoinflammation.
Torrelo A
Front Immunol; 2017; 8():927. PubMed ID: 28848544
[TBL] [Abstract][Full Text] [Related]
14. Periodontal Manifestations of Chronic Atypical Neutrophilic Dermatosis With Lipodystrophy and Elevated Temperature (CANDLE) Syndrome in an 11-Year-Old Patient.
McKenna GJ; Ziada HM
Clin Adv Periodontics; 2015 Aug; 5(3):153-158. PubMed ID: 32689728
[TBL] [Abstract][Full Text] [Related]
15. Proteasome assembly defect due to a proteasome subunit beta type 8 (PSMB8) mutation causes the autoinflammatory disorder, Nakajo-Nishimura syndrome.
Arima K; Kinoshita A; Mishima H; Kanazawa N; Kaneko T; Mizushima T; Ichinose K; Nakamura H; Tsujino A; Kawakami A; Matsunaka M; Kasagi S; Kawano S; Kumagai S; Ohmura K; Mimori T; Hirano M; Ueno S; Tanaka K; Tanaka M; Toyoshima I; Sugino H; Yamakawa A; Tanaka K; Niikawa N; Furukawa F; Murata S; Eguchi K; Ida H; Yoshiura K
Proc Natl Acad Sci U S A; 2011 Sep; 108(36):14914-9. PubMed ID: 21852578
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. A mutation in the immunoproteasome subunit PSMB8 causes autoinflammation and lipodystrophy in humans.
Kitamura A; Maekawa Y; Uehara H; Izumi K; Kawachi I; Nishizawa M; Toyoshima Y; Takahashi H; Standley DM; Tanaka K; Hamazaki J; Murata S; Obara K; Toyoshima I; Yasutomo K
J Clin Invest; 2011 Oct; 121(10):4150-60. PubMed ID: 21881205
[TBL] [Abstract][Full Text] [Related]
18. CANDLE syndrome: a recently described autoinflammatory syndrome.
Tüfekçi Ö; Bengoa Ş; Karapinar TH; Ataseven EB; İrken G; Ören H
J Pediatr Hematol Oncol; 2015 May; 37(4):296-9. PubMed ID: 25036278
[TBL] [Abstract][Full Text] [Related]
19. Identification of eight novel proteasome variants in five unrelated cases of proteasome-associated autoinflammatory syndromes (PRAAS).
Papendorf JJ; Ebstein F; Alehashemi S; Piotto DGP; Kozlova A; Terreri MT; Shcherbina A; Rastegar A; Rodrigues M; Pereira R; Park S; Lin B; Uss K; Möller S; da Silva Pina AF; Sztajnbok F; Torreggiani S; Niemela J; Stoddard J; Rosenzweig SD; Oler AJ; McNinch C; de Guzman MM; Fonseca A; Micheloni N; Fraga MM; Perazzio SF; Goldbach-Mansky R; de Jesus AA; Krüger E
Front Immunol; 2023; 14():1190104. PubMed ID: 37600812
[TBL] [Abstract][Full Text] [Related]
20. Rare hereditary autoinflammatory disorders: towards an understanding of critical in vivo inflammatory pathways.
Kanazawa N
J Dermatol Sci; 2012 Jun; 66(3):183-9. PubMed ID: 22336993
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
