BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

308 related articles for article (PubMed ID: 29159471)

  • 1. Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.
    Sighart R; Rech J; Hueber A; Blank N; Löhr S; Reis A; Sticht H; Hüffmeier U
    Rheumatol Int; 2018 Jan; 38(1):111-120. PubMed ID: 29159471
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Molecular genetic analysis for periodic fever syndromes: a supplemental role for the diagnosis of adult-onset Still's disease.
    Li H; Abramova I; Chesoni S; Yao Q
    Clin Rheumatol; 2018 Aug; 37(8):2021-2026. PubMed ID: 29909561
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Analysis of NLRP3, MVK and TNFRSF1A variants in adult Greek patients with autoinflammatory symptoms.
    Karagianni P; Nezos A; Ioakeim F; Tzioufas AG; Moutsopoulos HM
    Clin Exp Rheumatol; 2018; 36(6 Suppl 115):86-89. PubMed ID: 30418111
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Increased prevalence of MEFV exon 10 variants in Japanese patients with adult-onset Still's disease.
    Nonaka F; Migita K; Jiuchi Y; Shimizu T; Umeda M; Iwamoto N; Fujikawa K; Izumi Y; Mizokami A; Nakashima M; Ueki Y; Yasunami M; Kawakami A; Eguchi K
    Clin Exp Immunol; 2015 Mar; 179(3):392-7. PubMed ID: 25286988
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Molecular genetic evaluation of NLRP3, MVK and TNFRSF1A associated periodic fever syndromes.
    Ozyilmaz B; Kirbiyik O; Koc A; Ozdemir TR; Kaya Ozer O; Kutbay YB; Erdogan KM; Saka Guvenc M; Ozturk C
    Int J Immunogenet; 2019 Aug; 46(4):232-240. PubMed ID: 31135083
    [TBL] [Abstract][Full Text] [Related]  

  • 6. MEFV gene mutations and their clinical significance in Korean patients with adult-onset Still's disease.
    Kim JJ; Kim JK; Shim SC; Choe JY; Kim TH; Jun JB; Yoo DH
    Clin Exp Rheumatol; 2013; 31(3 Suppl 77):60-3. PubMed ID: 24064016
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Genetic profiling of autoinflammatory disorders in patients with periodic fever: a prospective study.
    De Pieri C; Vuch J; De Martino E; Bianco AM; Ronfani L; Athanasakis E; Bortot B; Crovella S; Taddio A; Severini GM; Tommasini A
    Pediatr Rheumatol Online J; 2015; 13():11. PubMed ID: 25866490
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.
    Cosan F; Emrence Z; Erbag G; Azakli H; Yilmazer B; Yazici A; Ekmekci SS; Abaci N; Ustek D; Cefle A
    Rheumatol Int; 2013 Jul; 33(7):1675-80. PubMed ID: 23269568
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Clinical and Genetic Features of Patients With TNFRSF1A Variants in Japan: Findings of a Nationwide Survey.
    Ueda N; Ida H; Washio M; Miyahara H; Tokunaga S; Tanaka F; Takahashi H; Kusuhara K; Ohmura K; Nakayama M; Ohara O; Nishikomori R; Minota S; Takei S; Fujii T; Ishigatsubo Y; Tsukamoto H; Tahira T; Horiuchi T
    Arthritis Rheumatol; 2016 Nov; 68(11):2760-2771. PubMed ID: 27332769
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Diagnostic utility of a targeted next-generation sequencing gene panel in the clinical suspicion of systemic autoinflammatory diseases: a multi-center study.
    Karacan İ; Balamir A; Uğurlu S; Aydın AK; Everest E; Zor S; Önen MÖ; Daşdemir S; Özkaya O; Sözeri B; Tufan A; Yıldırım DG; Yüksel S; Ayaz NA; Ömeroğlu RE; Öztürk K; Çakan M; Söylemezoğlu O; Şahin S; Barut K; Adroviç A; Seyahi E; Özdoğan H; Kasapçopur Ö; Turanlı ET
    Rheumatol Int; 2019 May; 39(5):911-919. PubMed ID: 30783801
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Evidence of digenic inheritance in autoinflammation-associated genes.
    Neocleous V; Byrou S; Toumba M; Costi C; Shammas C; Kyriakou C; Christophidou-Anastasiadou V; Tanteles GA; Hadjipanayis A; Phylactou LA
    J Genet; 2016 Dec; 95(4):761-766. PubMed ID: 27994174
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Human parvovirus B19 nonstructural protein NS1 activates NLRP3 inflammasome signaling in adult‑onset Still's disease.
    Chen DY; Chen YM; Chen HH; Hsieh CW; Gung NR; Hung WT; Tzang BS; Hsu TC
    Mol Med Rep; 2018 Feb; 17(2):3364-3371. PubMed ID: 29257322
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Neurological phenotypes in patients with NLRP3-, MEFV-, and TNFRSF1A low-penetrance variants.
    Mulazzani E; Wagner D; Havla J; Schlüter M; Meinl I; Gerdes LA; Kümpfel T
    J Neuroinflammation; 2020 Jun; 17(1):196. PubMed ID: 32563262
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Effects of HLA-DRB1 alleles on susceptibility and clinical manifestations in Japanese patients with adult onset Still's disease.
    Asano T; Furukawa H; Sato S; Yashiro M; Kobayashi H; Watanabe H; Suzuki E; Ito T; Ubara Y; Kobayashi D; Iwanaga N; Izumi Y; Fujikawa K; Yamasaki S; Nakamura T; Koga T; Shimizu T; Umeda M; Nonaka F; Yasunami M; Ueki Y; Eguchi K; Tsuchiya N; Tohma S; Yoshiura KI; Ohira H; Kawakami A; Migita K
    Arthritis Res Ther; 2017 Sep; 19(1):199. PubMed ID: 28899403
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A case of adult onset Still's disease with mutations of the MEFV gene who is partially responsive to colchicine.
    Ou-Yang LJ; Tang KT
    Medicine (Baltimore); 2018 Apr; 97(15):e0333. PubMed ID: 29642170
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Serum amyloid A1 (SAA1) gene polymorphisms in Japanese patients with adult-onset Still's disease.
    Yashiro M; Furukawa H; Asano T; Sato S; Kobayashi H; Watanabe H; Suzuki E; Nakamura T; Koga T; Shimizu T; Umeda M; Nonaka F; Ueki Y; Eguchi K; Kawakami A; Migita K
    Medicine (Baltimore); 2018 Dec; 97(49):e13394. PubMed ID: 30544414
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Association of Fcgamma receptor polymorphisms with adult onset Still's disease in Korea.
    Woo JH; Sung YK; Lee JS; Chung WT; Choe JY; Song GG; Yoo DH
    J Rheumatol; 2009 Feb; 36(2):347-50. PubMed ID: 19040302
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a novel heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF.
    Karacan İ; Uğurlu S; Tolun A; Tahir Turanlı E; Ozdogan H
    Clin Exp Rheumatol; 2017; 35 Suppl 108(6):75-81. PubMed ID: 29148404
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary autoinflammatory syndromes: a Brazilian multicenter study.
    Jesus AA; Fujihira E; Watase M; Terreri MT; Hilario MO; Carneiro-Sampaio M; Len CA; Oliveira SK; Rodrigues MC; Pereira RM; Bica B; Silva NA; Cavalcanti A; Marini R; Sztajnbok F; Quintero MV; Ferriani VP; Moraes-Vasconcelos D; Silva CA; Oliveira JB
    J Clin Immunol; 2012 Oct; 32(5):922-32. PubMed ID: 22566169
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetic Association and Expression Correlation between Colony-Stimulating Factor 1 Gene Encoding M-CSF and Adult-Onset Still's Disease.
    Chen YM; Hung WT; Chang WC; Hsieh CW; Chung WH; Lan JL; Gung NR; Lee YS; Chen DY; Hung SI
    J Immunol Res; 2020; 2020():8640719. PubMed ID: 32149159
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 16.