Pathological characterization of pachydermia in pachydermoperiostosis-Reference-Cited by-同舟云学术

Pathological characterization of pachydermia in pachydermoperiostosis

Published:2015-05-11 Issue:7 Volume:42 Page:710-714
ISSN:0385-2407
Container-title:The Journal of Dermatology
language:en
Short-container-title:J Dermatol

Author:

Tanese Keiji¹,Niizeki Hironori²,Seki Atsuhito³,Otsuka Atsushi⁴,Kabashima Kenji⁴,Kosaki Keisuke⁵,Kuwahara Masamitsu⁶,Miyakawa Shun‐ichi⁷,Miyasaka Mikiko⁸,Matsuoka Kentaro⁹,Okuyama Torayuki¹⁰,Shiohama Aiko¹¹,Sasaki Takashi¹²,Kudoh Jun¹¹,Amagai Masayuki¹,Ishiko Akira¹³

Affiliation:

1. Department of Dermatology Keio University School of MedicineTokyo Japan

2. Department of DermatologyNational Center for Child Health and DevelopmentTokyo Japan

3. Department of Orthopedics National Center for Child Health and Development TokyoJapan

4. Department of Dermatology Kyoto University Graduate School of Medicine KyotoJapan

5. Department of Orthopaedic Surgery University of Tokyo TokyoJapan

6. Department of Plastic Surgery Nara Medical University Hospital Kashihara NaraJapan

7. Division of Dermatology Kawasaki Municipal Hospital KanagawaJapan

8. Department of RadiologyNational Center for Child Health and DevelopmentTokyo Japan

9. Department of Pathology National Center for Child Health and DevelopmentTokyo Japan

10. Department of Clinical Laboratory Medicine National Center for Child Health and DevelopmentTokyo Japan

11. Laboratory of Gene Medicine Keio University School of MedicineTokyo Japan

12. Center for Integrated Medical Research Keio University School of MedicineTokyo Japan

13. Department of Dermatology Toho University School of Medicine Tokyo Japan

Publisher

Wiley

Subject

Dermatology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/1346-8138.12869

Reference7 articles.

1. Pachydermoperiostosis: an update

2. Identification of mutations in the prostaglandin transporter gene SLCO2A1 and its phenotype–genotype correlation in Japanese patients with pachydermoperiostosis

3. Exome Sequencing Identifies SLCO2A1 Mutations as a Cause of Primary Hypertrophic Osteoarthropathy

4. Prostaglandin E2 Increase in Pachydermoperiostosis Without 15-hydroprostaglandin Dehydrogenase Mutations

5. Complete form of pachydermoperiostosis: case report;Tanese K;Rinsho Hifuka,2010

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