1. Association of the TNFa13 microsatellite with systemic sclerosis in Japanese patients. Issue 4 (1st April 2000) Authors: Takeuchi, Fujio; Nabeta, Hiromi; Füssel, Monika; Conrad, Karsten; Frank, Karl-Heinz Journal: Annals of the rheumatic diseases Issue: Volume 59:Issue 4(2000) Page Start: 293 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Contribution of HLA‐B*51:01 and ‐A*26:01 to Behçet's disease and their clinical association in Thai patients. (15th January 2020) Authors: Louthrenoo, Worawit; Kasitanon, Nuntana; Pathanapitoon, Kessara; Wangkaew, Suparaporn; Kuwata, Shoji; Nishi, Ai; Kaburaki, Toshikatsu; Tanaka, Rie; Takeuchi, Fujio Journal: International journal of rheumatic diseases Issue: Volume 23:Number 2(2020) Page Start: 247 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. CTLA‐4 polymorphisms in Thai patients with rheumatoid arthritis, systemic lupus erythematosus, and systemic sclerosis. (17th September 2021) Authors: Louthrenoo, Worawit; Kasitanon, Nuntana; Wongthanee, Antika; Kuwata, Shoji; Takeuchi, Fujio Journal: International journal of rheumatic diseases Issue: Volume 24:Number 11(2021) Page Start: 1378 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. Determination of T Cell Responses in Thai Systemic Sclerosis Patients. (7th March 2022) Authors: Likhit, Oranit; Louthrenoo, Worawit; Pattanakitsakul, Sa-nga; Suttitheptumrong, Aroonroong; Hannongbua, Supot; Rungrotmongkol, Thanyada; Noguchi, Hiroshi; Takeuchi, Fujio; Boonnak, Kobporn Other Names: Xu Baohui Academic Editor. Journal: Journal of immunology research Issue: Volume 2022(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Genetic Association of a Gain‐of‐Function IFNGR1 Polymorphism and the Intergenic Region LNCAROD/DKK1 With Behçet's Disease. Issue 7 (18th May 2021) Authors: Ortiz Fernández, Lourdes; Coit, Patrick; Yilmaz, Vuslat; Yentür, Sibel P.; Alibaz‐Oner, Fatma; Aksu, Kenan; Erken, Eren; Düzgün, Nursen; Keser, Gokhan; Cefle, Ayse; Yazici, Ayten; Ergen, Andac; Alpsoy, Erkan; Salvarani, Carlo; Casali, Bruno; Kısacık, Bünyamin; Kötter, Ina; Henes, Jörg; Çınar, Muh... Journal: Arthritis & rheumatology Issue: Volume 73:Issue 7(2021) Page Start: 1244 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Sex-specific analysis in Behçet's disease reveals higher genetic risk in male patients. Issue 132 (October 2022) Authors: Jo, Yun Gun; Ortiz-Fernández, Lourdes; Coit, Patrick; Yilmaz, Vuslat; Yentür, Sibel P.; Alibaz-Oner, Fatma; Aksu, Kenan; Erken, Eren; Düzgün, Nursen; Keser, Gokhan; Cefle, Ayse; Yazici, Ayten; Ergen, Andac; Alpsoy, Erkan; Salvarani, Carlo; Kısacık, Bünyamin; Kötter, Ina; Henes, Jörg; Çınar, Muham... Journal: Journal of autoimmunity Issue: Issue 132(2022) Page Start: Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Spontaneous event of mitochondrial DNA mutation, A3243G, found in a family of identical twins. (April 2013) Authors: Harihara, Shinji; Nakamura, Kennichi; Takubo, Kaiyo; Takeuchi, Fujio Journal: Mitochondrial DNA Issue: Volume 24:Number 2(2013:Apr.) Page Start: 158 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗