HuGE Literature Finder
Records 1-26
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Clinical and genetic features of Chinese adult patients with tumour necrosis factor receptor-associated periodic fever syndrome.
Rheumatology (Oxford, England) 2019 Nov . Zhao Mengzhu, Luo Yi, Wu Di, Yang Yunjiao, Sun Yang, Wang Rongrong, Shen M |
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Evidence for genetic overlap between adult onset Still's disease and hereditary periodic fever syndromes.
Rheumatology international 2017 Nov . Sighart R, Rech J, Hueber A, Blank N, Löhr S, Reis A, Sticht H, Hüffmeier |
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Evidence of digenic inheritance in autoinflammation-associated genes.
Journal of genetics 2016 Dec 95 (4): 761-766. Neocleous Vassos, Byrou Stefania, Toumba Meropi, Costi Constantina, Shammas Christos, Kyriakou Christina, Christophidou-Anastasiadou Violetta, Tanteles George A, Hadjipanayis Adamos, Phylactou Leonidas |
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Clinical and Genetic Features of Korean Patients with Recurrent Fever and Multi-System Inflammation without Infectious or Autoimmune Evidence.
Journal of Korean medical science 2016 Feb 31 (2): 196-201. Yang Ji Ae, Choi Ji Yong, Kang Eun Ha, Ha You-Jung, Lee Yun Jong, Song Yeong Wo |
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TNFRSF1A Gene Causing Tumor Necrosis Factor Receptor-associated Periodic Syndrome in 2 Siblings Displaying Variable Disease Severity and Discordant Heterozygosity for an MEFV E148Q Variant.
The Journal of rheumatology 2015 Aug 42 (8): 1534-5. Abdwani Reem, Abdalla Eiman, Al Abrawi Safiya, Al-Thihli Khal |
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The phenotype of TNF receptor-associated autoinflammatory syndrome (TRAPS) at presentation: a series of 158 cases from the Eurofever/EUROTRAPS international registry.
Annals of the rheumatic diseases 2014 Dec 73 (12): 2160-7. Lachmann H J, Papa R, Gerhold K, Obici L, Touitou I, Cantarini L, Frenkel J, Anton J, Kone-Paut I, Cattalini M, Bader-Meunier B, Insalaco A, Hentgen V, Merino R, Modesto C, Toplak N, Berendes R, Ozen S, Cimaz R, Jansson A, Brogan P A, Hawkins P N, Ruperto N, Martini A, Woo P, Gattorno M, |
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Periodic fever, aphthous stomatitis, pharyngitis, cervical adenitis syndrome is linked to dysregulated monocyte IL-1? production.
The Journal of allergy and clinical immunology 2013 Jun 131 (6): 1635-43. Kolly Laeticia, Busso Nathalie, von Scheven-Gete Annette, Bagnoud Nathaliane, Moix Isabelle, Holzinger Dirk, Simon Gregoire, Ives Annette, Guarda Greta, So Alexander, Morris Michael A, Hofer Micha |
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Targeted resequencing implicates the familial Mediterranean fever gene MEFV and the toll-like receptor 4 gene TLR4 in Behçet disease.
Proceedings of the National Academy of Sciences of the United States of America 2013 May 110 (20): 8134-9. Kirino Yohei, Zhou Qing, Ishigatsubo Yoshiaki, Mizuki Nobuhisa, Tugal-Tutkun Ilknur, Seyahi Emire, Özyazgan Yilmaz, Ugurlu Serdal, Erer Burak, Abaci Neslihan, Ustek Duran, Meguro Akira, Ueda Atsuhisa, Takeno Mitsuhiro, Inoko Hidetoshi, Ombrello Michael J, Satorius Colleen L, Maskeri Baishali, Mullikin James C, Sun Hong-Wei, Gutierrez-Cruz Gustavo, Kim Yoonhee, Wilson Alexander F, Kastner Daniel L, Gül Ahmet, Remmers Elaine |
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Autoinflammatory gene polymorphisms and susceptibility to UK juvenile idiopathic arthritis.
Pediatric rheumatology online journal 2013 11 (1): 14. Hinks Anne, Martin Paul, Thompson Susan D, Sudman Marc, Stock Carmel J, Thomson Wendy, Day Thomas G, Packham Jon, , , Ramanan Athimalaipet V, Donn Rachelle |
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MEFV Variants in Patients with PFAPA Syndrome in Japan.
The open rheumatology journal 2013 7 22-5. Taniuchi Shoichiro, Nishikomori Ryuta, Iharada Anna, Tuji Shoji, Heike Toshio, Kaneko Kazuna |
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The association of TNFRSF1A gene and MEFV gene mutations with adult onset Still's disease.
Rheumatology international 2012 Dec . Cosan F, Emrence Z, Erbag G, Azakli H, Yilmazer B, Yazici A, Ekmekci SS, Abaci N, Ustek D, Cefle A |
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Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study.
Clinical research in cardiology : official journal of the German Cardiac Society 2012 Feb . Cantarini L, Lucherini OM, Brucato A, Barone L, Cumetti D, Iacoponi F, Rigante D, Brambilla G, Penco S, Brizi MG, Patrosso MC, Valesini G, Frediani B, Galeazzi M, Cimaz R, Paolazzi G, Vitale A, Imazio M |
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Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene.
Arthritis and rheumatism 2011 Apr 63 (4): 1141-50. Pelagatti M A, Meini A, Caorsi R, Cattalini M, Federici S, Zulian F, Calcagno G, Tommasini A, Bossi G, Sormani M P, Caroli F, Plebani A, Ceccherini I, Martini A, Gattorno |
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Role of the R92Q TNFRSF1A mutation in patients with familial Mediterranean fever.
Arthritis care & research 2010 Sep 62 (9): 1294-8. Marek-Yagel Dina, Berkun Yackov, Padeh Shai, Lidar Merav, Shinar Yael, Bar-Joseph Ifat, Reznik-Wolf Haike, Langevitz Pnina, Livneh Avi, Pras El |
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The 423Q polymorphism of the X-linked inhibitor of apoptosis gene influences monocyte function and is associated with periodic fever.
Arthritis and rheumatism 2009 Nov 60 (11): 3476-84. Ferretti Massimo, Gattorno Marco, Chiocchetti Annalisa, Mesturini Riccardo, Orilieri Elisabetta, Bensi Thea, Sormani Maria Pia, Cappellano Giuseppe, Cerutti Elisa, Nicola Stefania, Biava Alessandra, Bardelli Claudio, Federici Silvia, Ceccherini Isabella, Baldi Maurizia, Santoro Claudio, Dianzani Irma, Martini Alberto, Dianzani Umber |
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Incidence of TNFRSF1A mutations in German children: epidemiological, clinical and genetic characteristics.
Rheumatology (Oxford, England) 2009 Jun . Lainka E, Neudorf U, Lohse P, Timmann C, Stojanov S, Huss K, Kries RV, Niehues T |
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A diagnostic score for molecular analysis of hereditary autoinflammatory syndromes with periodic fever in children.
Arthritis and rheumatism 2008 Jun 58 (6): 1823-32. Gattorno M, Sormani M P, D'Osualdo A, Pelagatti M A, Caroli F, Federici S, Cecconi M, Solari N, Meini A, Zulian F, Obici L, Breda L, Martino S, Tommasini A, Bossi G, Govers A, Touitou I, Woo P, Frenkel J, Koné-Paut I, Baldi M, Ceccherini I, Martini |
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Late-onset tumor necrosis factor receptor-associated periodic syndrome in multiple sclerosis patients carrying the TNFRSF1A R92Q mutation.
Arthritis and rheumatism 2007 Aug 56 (8): 2774-83. Kümpfel Tania, Hoffmann Lisa-Ann, Rübsamen Heike, Pöllmann Walter, Feneberg Wolfgang, Hohlfeld Reinhard, Lohse Pet |
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Polymorphisms in proinflammatory genes and susceptibility to typhoid fever and paratyphoid fever.
Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research 2007 Apr 27 (4): 271-9. Ali Soegianto, Vollaard Albert M, Kremer Dennis, de Visser Adriëtte W, Martina Cerithsa A E, Widjaja Suwandhi, Surjadi Charles, Slagboom Eline, van de Vosse Esther, van Dissel Jaap |
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Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes.
Rheumatology (Oxford, England) 2006 Mar 45 (3): 269-73. Simon A, van der Meer J W M, Vesely R, Myrdal U, Yoshimura K, Duys P, Drenth J P H, |
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Unexpected high frequency of P46L TNFRSF1A allele in sub-Saharan West African populations.
European journal of human genetics : EJHG 2005 Apr 13 (4): 513-5. Tchernitchko Dimitri, Chiminqgi Mihelaiti, Galactéros Frédéric, Préhu Claude, Segbena Yvon, Coulibaly Hamidou, Rebaya Nadia, Loric Sylva |
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Allelic variants in genes associated with hereditary periodic fever syndromes as susceptibility factors for reactive systemic AA amyloidosis.
Genes and immunity 2004 Jun 5 (4): 289-93. Aganna E, Hawkins P N, Ozen S, Pettersson T, Bybee A, McKee S A, Lachmann H J, Karenko L, Ranki A, Bakkaloglu A, Besbas N, Topaloglu R, Hoffman H M, Hitman G A, Woo P, McDermott M |
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Mutational spectrum in the MEFV and TNFRSF1A genes in patients suffering from AA amyloidosis and recurrent inflammatory attacks.
Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association 2002 Jul 17 (7): 1212-7. Dodé Catherine, Hazenberg Bouke P C, Pêcheux Christophe, Cattan Daniel, Moulin Bruno, Barthélémy Anne, Gubler Marie-Claire, Delpech Marc, Grateau Gill |
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Idiopathic recurrent pericarditis refractory to colchicine treatment can reveal tumor necrosis factor receptor-associated periodic syndrome.
International journal of immunopathology and pharmacology 0 22 (4): 1051-8. Cantarini L, Lucherini O M, Cimaz R, Baldari C T, Bellisai F, Rossi Paccani S, Laghi Pasini F, Capecchi P L, Sebastiani G D, Galeazzi |
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MEFV, TNFRSF1A and CARD15 mutation analysis in Behçet's disease.
Clinical and experimental rheumatology 0 29 (4 Suppl 67): S24-7. Baruch Yoav, Dagan Efrat, Rosner Itzhak, Fiorilli Massimo, Gershoni-Baruch Ruth, Rozenbaum Micha |
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Validation of a diagnostic score for the diagnosis of autoinflammatory diseases in adults.
International journal of immunopathology and pharmacology 0 24 (3): 695-702. Cantarini Luca, Iacoponi F, Lucherini O M, Obici L, Brizi M G, Cimaz R, Rigante D, Benucci M, Sebastiani G D, Brucato A, Sabadini L, Simonini G, Giani T, Laghi Pasini F, Baldari C T, Bellisai F, Valentini G, Bombardieri S, Paolazzi G, Galeazzi |
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- Page last updated:Jan 16, 2020
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