1. A compound synonymous mutation c.474G>A with p.Arg578X mutation in SPINK5 causes splicing disorder and mild phenotype in Netherton syndrome. Issue 7 (20th May 2016) Authors: Numata, Sanae; Teye, Kwesi; Krol, Rafal P.; Okamatsu, Yuki; Hashikawa, Keiko; Matsuda, Mitsuhiro; Fortugno, Paola; Di Zenzo, Giovanni; Castiglia, Daniele; Zambruno, Giovanna; Hamada, Takahiro; Hashimoto, Takashi Journal: Experimental dermatology Issue: Volume 25:Issue 7(2016) Page Start: 568 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. A founder deletion of corneodesmosin gene (CDSN) is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases. Issue 2 (May 2017) Authors: Teye, Kwesi; Suga, Yasushi; Numata, Sanae; Soejima, Mikiko; Ishii, Norito; Krol, Rafal_P.; Ohata, Chika; Matsuda, Mitsuhiro; Honma, Masaru; Ishida-Yamamoto, Akemi; Hamada, Takahiro; Koda, Yoshiro; Hashimoto, Takashi Journal: Journal of dermatological science Issue: Volume 86:Issue 2(2017:May) Page Start: e52 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. A founder deletion of corneodesmosin gene is prevalent in Japanese patients with peeling skin disease: Identification of 2 new cases. Issue 2 (May 2016) Authors: Teye, Kwesi; Suga, Yasushi; Numata, Sanae; Soejima, Mikiko; Ishii, Norito; Krol, Rafal P.; Ohata, Chika; Matsuda, Mitsuhiro; Honma, Masaru; Ishida-Yamamoto, Akemi; Hamada, Takahiro; Koda, Yoshiro; Hashimoto, Takashi Journal: Journal of dermatological science Issue: Volume 82:Issue 2(2016:May) Page Start: 134 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. A three‐dimensional in vitro culture model of Hailey‐Hailey disease. Issue 10 (18th August 2015) Authors: Matsuda, Mitsuhiro; Hamada, Takahiro; Numata, Sanae; Teye, Kwesi; Ishii, Norito; Ohata, Chika; Furumura, Minao; Nakama, Takekuni; Hashimoto, Takashi Journal: Experimental dermatology Issue: Volume 24:Issue 10(2015:Oct.) Page Start: 788 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Anti‐early endosome antigen 1 autoantibodies were detected in a pemphigus‐like patient but not in the majority of pemphigus diseases. Issue 5 (May 2016) Authors: Nishikawa, Ryuhei; Takahashi, Hitoshi; Matsuda, Mitsuhiro; Imaoka, Kaoru; Ogawa, Masahiro; Teye, Kwesi; Tsuchisaka, Atsunari; Koga, Hiroshi; Komorowski, Lars; Probst, Christian; Hachiya, Takahisa; Fritzler, Marvin J.; Ishii, Norito; Ohata, Chika; Furumura, Minao; Krol, Rafal P.; Muro, Yoshinao; M... Journal: Experimental dermatology Issue: Volume 25:Issue 5(2016) Page Start: 368 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
6. Atypical pemphigus with immunoglobulin G autoantibodies against desmoglein 3 and desmocollin 3. Issue 4 (2nd September 2015) Authors: Kamiya, Koji; Aoyama, Yumi; Wakashima, Chie; Kudo, Tomoko; Nakajima, Kimiko; Sano, Shigetoshi; Ishii, Norito; Teye, Kwesi; Hashimoto, Takashi; Iwatsuki, Keiji; Tokura, Yoshiki Journal: Journal of dermatology Issue: Volume 43:Issue 4(2016) Page Start: 429 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
7. Case of paraneoplastic pemphigus with immunoglobulin (Ig)G and IgA antibodies to various antigens. Issue 8 (11th March 2016) Authors: Otsuka, Yohei; Ueno, Takashi; Yamase, Aya; Ito, Michiko; Osada, Shinichi; Kawana, Seiji; Funasaka, Yoko; Teye, Kwesi; Ishii, Norito; Hashimoto, Takashi; Saeki, Hidehisa Journal: Journal of dermatology Issue: Volume 43:Issue 8(2016) Page Start: 944 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
8. Corrigendum to 'Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia' [Journal of Dermatological Science 78 (2015) 82–85]. Issue 2 (August 2015) Authors: Numata, Sanae; Teye, Kwesi; Krol, Rafal P.; Karashima, Tadashi; Fukuda, Shunpei; Matsuda, Mitsuhiro; Ishii, Norito; Furumura, Minao; Ohata, Chika; Saminathan, Sasi D.; Ariffin, Roziana; Pramono, Zacharias A.D.; Leong, Kin Fon; Hamada, Takahiro; Hashimoto, Takashi Journal: Journal of dermatological science Issue: Volume 79:Issue 2(2015:Aug.) Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
9. Corrigendum to 'Mutation study for 9 genes in 23 unrelated patients with autosomal recessive congenital ichthyosis in Japan and Malaysia' [Journal of Dermatological Science 78 (2015) 82–85]. Issue 2 (August 2015) Authors: Numata, Sanae; Teye, Kwesi; Krol, Rafal P.; Karashima, Tadashi; Fukuda, Shunpei; Matsuda, Mitsuhiro; Ishii, Norito; Furumura, Minao; Ohata, Chika; Saminathan, Sasi D.; Ariffin, Roziana; Pramono, Zacharias A.D.; Leong, Kin Fon; Hamada, Takahiro; Hashimoto, Takashi Journal: Journal of dermatological science Issue: Volume 79:Issue 2(2015:Aug.) Page Start: 179 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
10. Dermoscopic furrow ink test of the palmar lesion in loricrin keratoderma. Issue 8 (25th April 2022) Authors: Shirahama, Toshihiro; Hamada, Takahiro; Abe, Toshifumi; Arakawa, Masataka; Teye, Kwesi; Koga, Hiroshi; Ishii, Norito; Nakama, Takekuni Journal: Journal of dermatology Issue: Volume 49:Issue 8(2022) Page Start: 783 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗