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1,234 results for MEFV

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Select record 21
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Association of MEFV mutations and vascular involvement in Behcet’s disease: a study from Hatay, Turkey
Author / Creator:Serarslan, Gamze ; Cura, Sibel ; Kimyon, Gezmiş ; Üçgül, Gökhan ; Karadağ, Mehmet
Publisher:Warsaw: Termedia Publishing House
Journal title:Reumatologia, 2022-01, Vol.60 (3), p.220-223
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Unresolved Issues in Familial Mediterranean Fever: Is p.R202Q MEFV Variant Potentially Pathogenetic in Unleashing Inflammation?
Author / Creator:Baggio, Chiara ; Oliviero, Francesca ; Galozzi, Paola ; Guidea, Irina ; Doria, Andrea ; Ramonda, Roberta ; Bindoli, Sara ; Sfriso, Paolo
Publisher:New York: Springer US
Journal title:Journal of clinical immunology, 2025-12, Vol.45 (1), p.104, Article 104
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Genotyping of familial Mediterranean fever gene (MEFV)—Single nucleotide polymorphism—Comparison of Nanopore with conventional Sanger sequencing
Author / Creator:Schmidt, Jonas ; Berghaus, Sandro ; Blessing, Frithjof ; Herbeck, Holger ; Blessing, Josef ; Schierack, Peter ; Rödiger, Stefan ; Roggenbuck, Dirk ; Wenzel, Folker
Publisher:United States: Public Library of Science
Journal title:PloS one, 2022-03, Vol.17 (3), p.e0265622
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A novel seven-tier framework for the classification of MEFV missense variants using adaptive and rigid classifiers
Author / Creator:Alay, Mustafa Tarık
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2025-03, Vol.15 (1), p.9054-23, Article 9054
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MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease
Author / Creator:Stoffels, Monique ; Szperl, Agata ; Simon, Anna ; Netea, Mihai G ; Plantinga, Theo S ; van Deuren, Marcel ; Kamphuis, Sylvia ; Lachmann, Helen J ; Cuppen, Edwin ; Kloosterman, Wigard P ; Frenkel, Joost ; van Diemen, Cleo C ; Wijmenga, Cisca ; van Gijn, Marielle ; van der Meer, Jos W M
Publisher:England: Elsevier Limited
Journal title:Annals of the rheumatic diseases, 2014-02, Vol.73 (2), p.455-461
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Sweet's Syndrome in Patients with MDS and MEFV Mutations
Author / Creator:Jo, Tatsuro ; Horio, Kensuke ; Migita, Kiyoshi
Publisher:United States: Massachusetts Medical Society
Journal title:The New England journal of medicine, 2015-02, Vol.372 (7), p.686-688
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MEFV gene mutations in neuro‐Behçet's disease and neuro‐Sweet disease
Author / Creator:Ishikawa, Hidehiro ; Shindo, Akihiro ; Ii, Yuichiro ; Kishida, Dai ; Niwa, Atsushi ; Nishiguchi, Yamato ; Matsuura, Keita ; Kato, Natsuko ; Mizutani, Akane ; Tachibana, Kei ; Hirata, Yoshinori ; Matsuyama, Hirofumi ; Ogawa‐Ito, Ai ; Taniguchi, Akira ; Tomimoto, Hidekazu
Publisher:United States: John Wiley & Sons, Inc
Journal title:Annals of clinical and translational neurology, 2019-12, Vol.6 (12), p.2595-2600
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Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants
Author / Creator:Honda Yoshitaka ; Maeda Yukako ; Izawa Kazushi ; Shiba Takeshi ; Tanaka, Takayuki ; Haruna, Nakaseko ; Nishimura Keisuke ; Mukoyama Hiroki ; Isa-Nishitani Masahiko ; Miyamoto Takayuki ; Nihira Hiroshi ; Shibata Hirofumi ; Hiejima Eitaro ; Ohara Osamu ; Takita Junko ; Yasumi Takahiro ; Nishikomori Ryuta
Publisher:New York: Springer Nature B.V
Journal title:Journal of clinical immunology, 2021-08, Vol.41 (6), p.1187-1197
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Recurrent pain attacks during romiplostim treatment in a patient with ITP carrying a heterozygous MEFV mutation
Author / Creator:Kinoshita, Shiori ; Komatsu, Hirokazu ; Fujinami, Haruna ; Yoshida, Takashi ; Suzuki, Tomotaka ; Narita, Tomoko ; Ito, Asahi ; Ri, Masaki ; Kusumoto, Shigeru ; Iida, Shinsuke
Publisher:Tokyo: Springer Nature B.V
Journal title:International journal of hematology, 2023-02, Vol.117 (2), p.283-286
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Possible Association of Mutations in the MEFV Gene with the Intestinal Phenotype of Behçet’s Disease and Refractoriness to Treatment
Author / Creator:Furuta, Yoki ; Gushima, Ryosuke ; Naoe, Hideaki ; Honda, Munenori ; Tsuruta, Yuiko ; Nagaoka, Katsuya ; Watanabe, Takehisa ; Tateyama, Masakuni ; Fujimoto, Nahoko ; Hirata, Shinya ; Miyagawa, Eiko ; Sakata, Komei ; Mizuhashi, Yumiko ; Iwakura, Mikako ; Murai, Masayuki ; Matsuoka, Masao ; Komohara, Yoshihiro ; Tanaka, Yasuhito
Publisher:Switzerland: MDPI AG
Journal title:Journal of clinical medicine, 2023-04, Vol.12 (9), p.3131
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Discontinuing colchicine in symptomatic carriers for MEFV (Mediterranean FeVer) variants
Author / Creator:Sönmez, Hafize Emine ; Batu, Ezgi Deniz ; Bilginer, Yelda ; Özen, Seza
Publisher:London: Springer London
Journal title:Clinical rheumatology, 2017-02, Vol.36 (2), p.421-425
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Does having MEFV gene sequence variants affect the clinical course and colchicine response in children with PFAPA syndrome?
Author / Creator:Otar Yener, Gülçin ; Aktaş, İlke ; Altıntaş Meşe, Ceren ; Çakan, Mustafa
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:European journal of pediatrics, 2023-01, Vol.182 (1), p.411-417
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Effect of Germline MEFV Polymorphisms on the Prognosis of Japanese Children with Cancer: A Regional Analysis
Author / Creator:Hasegawa, Morio ; Fukushima, Hiroko ; Suzuki, Ryoko ; Yamaki, Yuni ; Hosaka, Sho ; Inaba, Masako ; Nakao, Tomohei ; Kobayashi, Chie ; Yoshimi, Ai ; Tsuchida, Masahiro ; Koike, Kazutoshi ; Fukushima, Takashi ; Takada, Hidetoshi
Publisher:Basel, Switzerland: S. Karger AG
Journal title:Oncology, 2022-07, Vol.100 (7), p.376-383
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Gain-of-function of MEFV Mutation Causes Very Early Onset Inflammatory Bowel Disease
Author / Creator:Wang, Qintao ; Chen, Xiang ; Luo, Youyou ; Chen, Jie ; Yu, Xiaomin
Publisher:New York: Springer Nature B.V
Journal title:Journal of clinical immunology, 2023-08, Vol.43 (6), p.1165-1169
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P072 MEFV/miR-326 axis involvement in human macrophage polarization
Author / Creator:Robin, M ; Sarrabay, G ; Peynircioglu, B ; Ozen, S ; Touitou, I ; Duroux-Richard, I ; Apparailly, F
Publisher:Kidlington: Elsevier Limited
Journal title:Annals of the rheumatic diseases, 2019-03, Vol.78 (Suppl 1), p.A30-A31
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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium
Author / Creator:Fahrioglu, Umut ; Bakir-Gungor, Burcu ; Temel, Sehime Gulsun ; Artan, Sevilhan ; Cora, Tulin ; Sahin, Feride Iffet ; Dursun, Ahmet ; Sezer, Ozlem ; Gunduz, C. Nur Semerci ; Ozdemir, Ozturk ; Ulgenalp, Ayfer ; Bagis, Haydar ; Bozkurt, Gokay ; Arman, Ahmet ; Aymelek, Huri Sema ; Ruhi, Hatice Ilgin ; Ergoren, Mahmut Cerkez ; Altunoglu, Umut ; Yuksel, Berrin ; Ozkul, Yusuf ; Kenanoglu, Sercan ; Ozcelik, Firat ; Demir, Mikail ; Kulak, Hande ; Akalin, Hilal ; Colak, Fatma Kurt ; Aynekin, Busra ; Emekli, Rabia ; Senel, Abdurrahman Soner ; Poyrazoglu, Muammer Hakan ; Kisaarslan, Ayse Nur Pac ; Baskol, Mevlut ; Calis, Mustafa ; Demir, Huseyin ; Zararsiz, Gozde Erturk ; Solak, Mustafa ; Atasever, Umut ; Aliyeva, Lamiya ; Dogan, Berkcan ; Erguzeloglu, Cemre Ornek ; Cogulu, Ozgur ; Onay, Huseyin ; Karaca, Emin ; Aykut, Ayca ; Cilingir, Oguz ; Gokalp, Ebru Erzurumluoglu ; Arslan, Serap ; Temena, Arda ; Haziyeva, Konul ; Bas, Hasan ; Sarac, Elif ; Kocak, Nadir ; Nergiz, Suleyman ; Baskin, Esra Sidika ; Bahadir, Oguzhan ; Sanri, Aslihan ; Yigit, Serbulent ; Yalcintepe, Sinem ; Ozkayin, Nese ; Kiraz, Aslihan ; Balta, Burhan ; Kurt, E. Emre ; Ceylan, Gulay Gulec ; Ceylan, Ahmet Cevdet ; Boga, Ibrahim ; Yilmaz, Mustafa ; Silan, Fatma ; Kocabey, Mehmet ; Koc, Altug ; Bozkaya, Ozlem Giray ; Ercal, Derya ; Ergun, Mehmet Ali ; Ergun, Sezen Guntekin ; Duman, Yesim Sidar ; Beyazit, Serife Busra ; Uzel, Veysiye Hulya ; Eroz, Recep ; Demirtas, Mercan ; Kabayegit, Zehra Manav ; Altan, Mustafa ; Mardan, Lamiya ; Tunc, Betul ; Zamani, Aysegul ; Ates, Esra Arslan ; Clark, Ozden Altiok ; Coskun, Mert ; Emmungil, Hakan ; Gurakan, Figen ; Kebudi, Rejin ; Karabulut, Halil Gurhan ; Tuncali, Timur ; Kutlay, Nuket Yurur ; Tulay, Pinar ; Tosun, Ozgur ; Tuncel, Gulten ; Mocan, Gamze ; Kale, Hamdi ; Uyguner, Zehra Oya ; Acar, Aynur ; Erdem, Levent
Publisher:Heidelberg: Springer Nature B.V
Journal title:Functional & integrative genomics, 2022-06, Vol.22 (3), p.291-315
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Select record 37
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AB0983 Mefv mutations in armenian patients with systemic autoimmune diseases
Author / Creator:Ginosyan, K ; Beglaryan, A ; Vardanyan, V
Publisher:Kidlington: Elsevier Limited
Journal title:Annals of the rheumatic diseases, 2017-06, Vol.76 (Suppl 2), p.1398-1399
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Select record 38
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AB0727 STUDY OF MEFV GENE MUTATIONS IN A COHORT OF CHILDREN: A SINGLE CENTER
Author / Creator:Kriulina, T. ; Alexeeva, E. ; Dvoryakovskaya, T. ; Kriulin, I. ; Isaeva, K. ; Denisova, R. ; Lomakina, O. ; Mamutova, A. ; Chomakhidze, A. ; Fetisova, A. ; Gautier, M. ; Krekhova, E. ; Tsulukiya, I. ; Gromov, A.
Journal title:Annals of the rheumatic diseases, 2021-06, Vol.80, p.1394-1395
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Generation of iPSCs from a Patient with the M694V Mutation in the MEFV Gene Associated with Familial Mediterranean Fever and Their Differentiation into Macrophages
Author / Creator:Grigor’eva, Elena V. ; Karapetyan, Lana V. ; Malakhova, Anastasia A. ; Medvedev, Sergey P. ; Minina, Julia M. ; Hayrapetyan, Varduhi H. ; Vardanyan, Valentina S. ; Zakian, Suren M. ; Arakelyan, Arsen ; Zakharyan, Roksana
Publisher:Switzerland: MDPI AG
Journal title:International journal of molecular sciences, 2024-06, Vol.25 (11), p.6102
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Select record 40
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THU0400 Familial Mediterranean Fever Gene (MEFV) Mutations and Disease Severity in Systemic Lupus Erythematosus (SLE); Implications on the Role of the E148Q MEFV Allele on Inflammation
Author / Creator:Deniz, R. ; Ozen, G. ; Yilmaz-Oner, S. ; Alibaz-Oner, F. ; Eren, F. ; Alhan, O. ; Inanc, N. ; Direskeneli, H. ; Atagunduz, P.
Publisher:Kidlington: Elsevier Limited
Journal title:Annals of the rheumatic diseases, 2014-06, Vol.73 (Suppl 2), p.320
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Showing 21 to 40 of 1,234 results

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Association of MEFV mutations and vascular involvement in Behcet’s disease: a study from Hatay, Turkey

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Unresolved Issues in Familial Mediterranean Fever: Is p.R202Q MEFV Variant Potentially Pathogenetic in Unleashing Inflammation?

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Genotyping of familial Mediterranean fever gene (MEFV)—Single nucleotide polymorphism—Comparison of Nanopore with conventional Sanger sequencing

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A novel seven-tier framework for the classification of MEFV missense variants using adaptive and rigid classifiers

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MEFV mutations affecting pyrin amino acid 577 cause autosomal dominant autoinflammatory disease

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Sweet's Syndrome in Patients with MDS and MEFV Mutations

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MEFV gene mutations in neuro‐Behçet's disease and neuro‐Sweet disease

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Rapid Flow Cytometry-Based Assay for the Functional Classification of MEFV Variants

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Recurrent pain attacks during romiplostim treatment in a patient with ITP carrying a heterozygous MEFV mutation

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Possible Association of Mutations in the MEFV Gene with the Intestinal Phenotype of Behçet’s Disease and Refractoriness to Treatment

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Discontinuing colchicine in symptomatic carriers for MEFV (Mediterranean FeVer) variants

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Does having MEFV gene sequence variants affect the clinical course and colchicine response in children with PFAPA syndrome?

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Effect of Germline MEFV Polymorphisms on the Prognosis of Japanese Children with Cancer: A Regional Analysis

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Gain-of-function of MEFV Mutation Causes Very Early Onset Inflammatory Bowel Disease

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P072 MEFV/miR-326 axis involvement in human macrophage polarization

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Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium

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AB0983 Mefv mutations in armenian patients with systemic autoimmune diseases

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AB0727 STUDY OF MEFV GENE MUTATIONS IN A COHORT OF CHILDREN: A SINGLE CENTER

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Generation of iPSCs from a Patient with the M694V Mutation in the MEFV Gene Associated with Familial Mediterranean Fever and Their Differentiation into Macrophages

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THU0400 Familial Mediterranean Fever Gene (MEFV) Mutations and Disease Severity in Systemic Lupus Erythematosus (SLE); Implications on the Role of the E148Q MEFV Allele on Inflammation

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