Recurrent pericarditis caused by a rare mutation in the TNFRSF1A gene and with excellent response to anakinra treatment
Cantarini, L.; Lucherini, O.M.; Cimaz, R.; Galeazzi, M.
Clinical and Experimental Rheumatology 28(5): 802
2010
ISSN/ISBN: 0392-856X PMID: 21029567 Document Number: 638328
Document emailed within 1 workday
Related Documents
Cantarini, L.; Lucherini, O.M.; Galeazzi, M.; Fanti, F.; Simonini, G.; Baldari, C.T.; Laghi Pasini, F.; De Martino, M.; Cimaz, R. 2009: Tumour necrosis factor receptor-associated periodic syndrome caused by a rare mutation in the TNFRSF1A gene, and with excellent response to etanercept treatment Clinical and Experimental Rheumatology 27(5): 890-891Lumpaopong, A.; Thirakhupt, P.; Srisuwan, K.; Chulamokha, Y. 2009: Rare F311L CFTR gene mutation in a child presented with recurrent electrolyte abnormalities and metabolic alkalosis: case report Journal of the Medical Association of Thailand 92(5): 694-698
Shenoy, V.V.; Joshi, S.R.; Kotwal, V.S.; Shedge, R.T.; Ramraje, N.N.; Lanjewar, D.N. 2006: Recurrent Kimura's disease: excellent response to cyclosporine Journal of the Association of Physicians of India 54: 153-155
Al-Mutairi, N.; Joshi, A.; Nour-Eldin, O. 2005: Punctate palmoplantar keratoderma (Buschke-Fischer-Brauer disease) with psoriasis: a rare association showing excellent response to acitretin Journal of drugs in dermatology: JDD 4(5): 627-634
Gayet, C.; Villard, J.; Andre-Fouët, X.; Baulieux, J.; Ducreux, J.C.; Tempelhoff, G.; Buisson, P.; Vial, P.; Guérin, J.C.; Pont, M. 1984: Superior vena caval thrombosis and recurrent pericarditis caused by a bronchogenic cyst Journal of Cardiovascular Surgery 25(1): 86-89
Tao, K.; Yasutomo, K. 2005: SLE caused by DNase 1 gene mutation Nihon Rinsho. Japanese Journal of Clinical Medicine 63(Suppl 5): 205-209
Keller, D.I.; Barrane, F-Zahara.; Gouas, L.; Martin, J.; Pilote, S.; Suarez, V.; Osswald, S.; Brink, M.; Guicheney, P.; Schwick, N.; Chahine, M. 2005: A novel nonsense mutation in the SCN5A gene leads to Brugada syndrome and a silent gene mutation carrier state Canadian Journal of Cardiology 21(11): 925-931
Barriales Alvarez, V.; Rodríguez Blanco, V.M. 1994: Colchicine in the treatment of recurrent pericarditis Medicina Clinica 103(19): 739-740
Meral, C.; Malbora, B.; Celikel, F.; Aydemir, G.ök.; Süleymanoğlu, S.; Zollino, M.; Derbent, M. 2012: A case of Mowat-Wilson syndrome caused by a truncating mutation within exon 8 of the ZEB2 gene Turkish Journal of Pediatrics 54(5): 523-527
Sforza, G.; Targa, L.; Resta, M.; Vaglio, A.; Martines, M.; Martines, C. 1995: Colchicine in the treatment of idiopathic recurrent pericarditis. Report of a case Minerva Cardioangiologica 43(6): 281-285
Rodríguez, V.M.; Barriales, V.; Morís, C.; Lambert, J.L.; Barriales, R.; Trabanco, I.M. 1995: Colchicine in the treatment of steroid-dependent recurrent idiopathic pericarditis Anales de Medicina Interna 12(2): 101-102
Zakliaz'minskaia, E.V.; Shestak, A.G.; Revishvili, A.S.; Pronicheva, I.V.; Podoliak, D.G.; Nechaenko, M.A.; Poliakov, A.V.; Dzemeshkevich, S.L. 2013: Clinic and genetic polymorphism of Brugada syndrome in Russian patients, caused by mutation in SCN5A gene Khirurgiia 2: 49-53
Stuhrmann, M.; Bukhari, I.A.; El-Harith, E-Harith.A. 2004: Naxos disease in an Arab family is not caused by the Pk2157del2 mutation. Evidence for exclusion of the plakoglobin gene Saudi Medical Journal 25(10): 1449-1452
Sangkhathat, S.; Kanngurn, S.; Jaruratanasirikul, S.; Tubtawee, T.; Chaiyapan, W.; Patrapinyokul, S.; Chiengkriwate, P. 2010: Peripheral precocious puberty in a male caused by Leydig cell adenoma harboring a somatic mutation of the LHR gene: report of a case Journal of the Medical Association of Thailand 93(9): 1093-1097
Henri, A.; Welsch, W.; Klastersky, J. 1973: Surgical treatment of heart tamponade caused by a neoplastic pericarditis Acta Cardiologica 28(1): 95-98
Elias-Assad, G.; Elias, M.; Kanety, H.; Pressman, A.; Tenenbaum-Rakover, Y. 2016: Persistent Müllerian Duct Syndrome Caused by a Novel Mutation of an Anti-MüIlerian Hormone Receptor Gene: Case Presentation and Literature Review Pediatric Endocrinology Reviews: Per 13(4): 731-740
Zhu, J.; Luo, D.; Shen, C.-h.; Xu, J. 2007: Photo-protection of epigallocatechin-3-gallate on aging and gene mutation of human skin fibroblasts caused by ultraviolet radiation: an in vitro experiment Zhonghua Yi Xue Za Zhi 87(20): 1398-1401
Zilfalil, B.A.; Sarina, S.; Liza-Sharmini, A.T.; Oldfield, N.J.; Stenhouse, S.A. 2006: Detection of F508del mutation in cystic fibrosis transmembrane conductance regulator gene mutation among Malays Singapore Medical Journal 47(2): 129-133
George, E.; Jama, T.; Azian, A.S.N.; Rahimah, A.; Zubaidah, Z. 2009: A rare case of alpha-thalassaemia intermedia in a Malay patient double heterozygous for alpha(+)-thalassaemia and a mutation in alpha1 globin gene CD59 (GGC --> GAC) Medical Journal of Malaysia 64(4): 321-322
Kawamura, J.; Kato, S.; Ishihara, T.; Hiraishi, Y.; Kawashiro, T. 1997: Difference of new mutation rates in dystrophin gene between deletion and duplication mutation in Duchenne and Becker muscular dystrophy Rinsho Shinkeigaku 37(3): 212-217