Recent Advances in Clinical Research on Rare Intractable Hereditary Skin Diseases in Japan-Reference-Cited by-同舟云学术

Recent Advances in Clinical Research on Rare Intractable Hereditary Skin Diseases in Japan

Published:2023 Issue: Volume: Page:
ISSN:0022-9717
Container-title:The Keio Journal of Medicine
language:en
Short-container-title:Keio J. Med.

Author:

Akiyama Masashi¹,Takeichi Takuya¹,Ikeda Shigaku²,Ishiko Akira³,Kurosawa Michiko⁴,Murota Hiroyuki⁵,Shimomura Yutaka⁶,Suzuki Tamio⁷,Tamai Katsuto⁸,Tanaka Akio⁹,Terui Tadashi¹⁰,Amagai Masayuki¹¹

Affiliation:

1. Department of Dermatology, Nagoya University Graduate School of Medicine, Nagoya, Japan

2. Department of Dermatology and Allergology, Juntendo University Graduate School of Medicine, Tokyo, Japan

3. Department of Dermatology, Toho University School of Medicine, Tokyo, Japan

4. Department of Epidemiology and Environmental Health, Juntendo University Faculty of Medicine, Tokyo, Japan

5. Department of Dermatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan

6. Department of Dermatology, Yamaguchi University Graduate School of Medicine, Ube, Japan

7. Department of Dermatology, Yamagata University Faculty of Medicine, Yamagata, Japan

8. Department of Stem Cell Therapy Science, Osaka University Graduate School of Medicine, Suita, Osaka, Japan

9. Department of Dermatology, Graduate School of Biomedical and Health Sciences, Hiroshima University, Hiroshima, Japan

10. Division of Cutaneous Science, Department of Dermatology, Nihon University School of Medicine, Tokyo, Japan

11. Laboratory for Skin Homeostasis, RIKEN Center for Integrative Medical Sciences, Kanagawa, Japan

Publisher

Keio Journal of Medicine

Subject

General Medicine

Link

https://www.jstage.jst.go.jp/article/kjm/advpub/0/advpub_2023-0008-IR/_pdf

Reference37 articles.

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2. 2. Yoshida K, Kobayashi M, Matsunaga Y, Kubo A, Ishiko A: Case of intermediate recessive dystrophic epidermolysis bullosa with negative LH7.2 staining. J Dermatol 2020; 47: e370–e372. PMID:32656782 https://doi.org/10.1111/1346-8138.15498

3. 3. Mori S, Shimbo T, Kimura Y, Hayashi M, Kiyohara E, Fukui M, Watanabe M, Bessho K, Fujimoto M, Tamai K: Recessive dystrophic epidermolysis bullosa with extensive transplantation of cultured epidermal autograft product after cardiopulmonary resuscitation: a case report. J Dermatol 2021; 48: e194–e195. PMID:33609402 https://doi.org/10.1111/1346-8138.15798

4. 4. Fujita Y, Nohara T, Takashima S, Natsuga K, Adachi M, Yoshida K, Shinkuma S, Takeichi T, Nakamura H, Wada O, Akiyama M, Ishiko A, Shimizu H: Intravenous allogeneic multilineage‐differentiating stress‐enduring cells in adults with dystrophic epidermolysis bullosa: a phase 1/2 open‐label study. J Eur Acad Dermatol Venereol 2021; 35: e528–e531. PMID:33656198 https://doi.org/10.1111/jdv.17201

5. 5. Takaki S, Shimbo T, Ikegami K, Kitayama T, Yamamoto Y, Yamazaki S, Mori S, Tamai K: Generation of a recessive dystrophic epidermolysis bullosa mouse model with patient-derived compound heterozygous mutations. Lab Invest 2022; 102: 574–580. PMID:35152273 https://doi.org/10.1038/s41374-022-00735-5

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