1. 3071 A phase II study of carboplatin (Cb), pemetrexed (PEM), and bevacizumab (Bev) followed by Bev and erlotinib (Erl) maintenance for non-squamous non-small cell lung cancer (NS-NSCLC) with wild-type (WT) EGFR. (September 2015) Authors: Takashina, T.; Asahina, H.; Yamada, N.; Harada, M.; Nakano, K.; Yokouchi, H.; Kanazawa, K.; Takamura, K.; Ogi, T.; Harada, T.; Honjo, O.; Morikawa, N.; Kinoshita, I.; Honda, R.; Amano, T.; Akita, H.; Isobe, H.; Nishimura, M. Journal: European journal of cancer Issue: Volume 51:(2015)Supplement 3 Page Start: S620 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease. (13th October 2019) Authors: Takeichi, T.; Matsumoto, T.; Nomura, T.; Takeda, M.; Niwa, H.; Kono, M.; Shimizu, H.; Ogi, T.; Akiyama, M. Journal: British journal of dermatology Issue: Volume 182:Number 2(2020) Page Start: 491 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A novel NCSTN missense mutation in the signal peptide domain causes hidradenitis suppurativa, which has features characteristic of an autoinflammatory keratinization disease. (1st February 2020) Authors: Takeichi, T.; Matsumoto, T.; Nomura, T.; Takeda, M.; Niwa, H.; Kono, M.; Shimizu, H.; Ogi, T.; Akiyama, M. Journal: British journal of dermatology Issue: Volume 182:Number 2(2020) Page Start: 491 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. An XPA gene splicing mutation resulting in trace protein expression in an elderly patient with xeroderma pigmentosum group A without neurological abnormalities. (19th May 2017) Authors: Takahashi, Y.; Endo, Y.; Kusaka‐Kikushima, A.; Nakamaura, S.; Nakazawa, Y.; Ogi, T.; Uryu, M.; Tsuji, G.; Furue, M.; Moriwaki, S. Journal: British journal of dermatology Issue: Volume 177:Number 1(2017) Page Start: 253 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. An XPA gene splicing mutation resulting in trace protein expression in an elderly patient with xeroderma pigmentosum group A without neurological abnormalities. (1st July 2017) Authors: Takahashi, Y.; Endo, Y.; Kusaka‐Kikushima, A.; Nakamaura, S.; Nakazawa, Y.; Ogi, T.; Uryu, M.; Tsuji, G.; Furue, M.; Moriwaki, S. Journal: British journal of dermatology Issue: Volume 177:Number 1(2017) Page Start: 253 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Epithelioid cell granuloma formation in CARD14‐associated papulosquamous eruptions. (29th December 2021) Authors: Takeichi, T.; Ikeda, K.; Muro, Y.; Ogi, T.; Morizane, S.; Akiyama, M. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 5(2022) Page Start: e369 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. MEDNIK‐like syndrome due to compound heterozygous mutations in AP1B1. (6th January 2021) Authors: Ito, Y.; Takeichi, T.; Igari, S.; Mori, T.; Ono, A.; Suyama, K.; Takeuchi, S.; Muro, Y.; Ogi, T.; Hosoya, M.; Yamamoto, T.; Akiyama, M. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 35:Number 5(2021) Page Start: e345 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Mutations in SAM syndrome and palmoplantar keratoderma patients suggest genotype/phenotype correlations in DSG1 mutations. (27th October 2021) Authors: Takeuchi, S.; Takeichi, T.; Koike, Y.; Takama, H.; Tanahashi, K.; Okuno, Y.; Ishii, N.; Muro, Y.; Ogi, T.; Suga, Y.; Akiyama, M. Journal: Journal of the European Academy of Dermatology and Venereology Issue: Volume 36:Number 3(2022) Page Start: e215 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗