Human Genome Epidemiology Literature Finder
Records 1 - 8 (of 8 Records) |
Query Trace: Uveitis and NOD2[original query] |
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Uveitis in patients with sarcoidosis is not associated with mutations in NOD2 (CARD15). American journal of ophthalmology 2003 Nov 136 (5): 933-5. Martin Tammy M, Doyle Trudy M, Smith Justine R, Dinulescu Denis, Rust Kristal, Rosenbaum James |
Blau syndrome-related CARD15/NOD2 mutations are not linked to idiopathic uveitis in Spanish patients. Disease markers 2009 27 (1): 1-5. Rodríguez-Pérez Noelia, Aguinaga-Barrilero Ana, Gorroño-Echebarría Marina B, Pérez-Blas Mercedes, Martín-Villa José |
Role of the NOD2 genotype in the clinical phenotype of Blau syndrome and early-onset sarcoidosis. Arthritis and rheumatism 2009 Jan 60 (1): 242-50. Okafuji Ikuo, Nishikomori Ryuta, Kanazawa Nobuo, Kambe Naotomo, Fujisawa Akihiro, Yamazaki Shin, Saito Megumu, Yoshioka Takakazu, Kawai Tomoki, Sakai Hidemasa, Tanizaki Hideaki, Heike Toshio, Miyachi Yoshiki, Nakahata Tatsutos |
Immunologic and genetic markers in patients with idiopathic ocular inflammation and a family history of inflammatory bowel disease. American journal of ophthalmology 2012 Jul 154 (1): 72-7. Abbasian Javaneh, Martin Tammy M, Patel Sarju, Tessler Howard H, Goldstein Debra |
Brief Report: First Identification of Intrafamilial Recurrence of Blau Syndrome due to Gonosomal NOD2 Mosaicism. Arthritis & rheumatology (Hoboken, N.J.) 2015 Nov . Mensa-Vilaro Anna, Cham Weng Tarng, Tang Swee Ping, Chin Lim Sern, González-Roca Eva, Ruiz-Ortiz Estibaliz, Ariffin Roziana, Yagüe Jordi, Aróstegui Juan |
[Mutations of NOD2 gene and clinical features in Chinese Blau syndrome patients]. Zhonghua er ke za zhi. Chinese journal of pediatrics 2014 Dec 52 (12): 896-901. Wang Wei, Wei Min, Song Hongmei, Qiu Zhengqi |
Genetic and Clinical Features of Blau Syndrome among Chinese Patients with Uveitis. Ophthalmology 2022 3 129 (7): 821-828. Zhong Zhenyu, Ding Jiadong, Su Guannan, Liao Weiting, Gao Yu, Zhu Yunyun, Deng Yang, Li Fuzhen, Du Liping, Gao Yuan, Yang Peize |
Blau Syndrome: Challenging Molecular Genetic Diagnostics of Autoinflammatory Disease. Genes 2024 6 15 (6): . Michaela Brichova, Aneta Klimova, Jarmila Heissigerova, Petra Svozilkova, Manuela Vaneckova, Pavla Dolezalova, Dana Nemcova, Marcela Michalickova, Jana Jedlickova, Lubica Dudakova, Petra Lisko |
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