HuGE Literature Finder
Records
1
-
9
| Multiple Sclerosis patients carry an increased burden of exceedingly rare genetic variants in the inflammasome regulatory genes. Scientific reports 2019 Jun 9 (1): 9171. Vidmar Lovro, Maver Ales, Drulovic Jelena, Sepcic Juraj, Novakovic Ivana, Ristic Smiljana, Šega Saša, Peterlin Bor |
| TNFRSF1A and MEFV mutations in childhood onset multiple sclerosis. European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society 2017 Sep . Blaschek Astrid, V Kries Rüdiger, Lohse Peter, Huss Kristina, Vill Katharina, Belohradsky Bernd H, Heinen Florian, Müller-Felber Wolfgang, Kümpfel Tan |
| The relationship between familial Mediterranean fever gene (MEFV) mutations and clinical and radiologic parameters in multiple sclerosis patients. The International journal of neuroscience 2015 Feb 125 (2): 116-22. Terzi Murat, Task?n Emre, Unal Akdemir Neslihan, Bagc? Hasan, Onar Mu |
| Rare MEFV variants are not associated with risk to develop multiple sclerosis and severity of disease. Multiple sclerosis (Houndmills, Basingstoke, England) 2013 Aug 19 (9): 1132-6. Pauwels Ine, Cosemans Leentje, Boonen Steven, Dubois Bénédicte, Goris |
| Association of missense mutations of Mediterranean fever (MEFV) gene with multiple sclerosis in Turkish population. Journal of molecular neuroscience : MN 2013 Jan . Yigit S, Karakus N, Kurt SG, Ates O |
| Familial Mediterranean fever-associated mutation pyrin E148Q as a potential risk factor for multiple sclerosis. Multiple sclerosis (Houndmills, Basingstoke, England) 2012 Sep 18 (9): 1229-38. Kümpfel T, Gerdes L-A, Wacker T, Blaschek A, Havla J, Krumbholz M, Pöllmann W, Feneberg W, Hohlfeld R, Lohse |
| Evaluation of common mutations in the Mediterranean fever gene in Multiple Sclerosis patients: is it a susceptibility gene? Journal of the neurological sciences 2010 Jul 294 (1-2): 38-42. Unal Aysun, Dursun Ahmet, Emre Ufuk, Tascilar Nida F, Ankarali Hand |
| 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 |
| Common mutations in the familial Mediterranean fever gene associate with rapid progression to disability in non-Ashkenazi Jewish multiple sclerosis patients. Genes and immunity 2003 Apr 4 (3): 197-203. Shinar Y, Livneh A, Villa Y, Pinhasov A, Zeitoun I, Kogan A, Achiron |
- Page last reviewed:Oct 1, 2021
- Page last updated:May 26, 2022
- Content source: