Genetic Disorders with Dyshidrosis: Ectodermal Dysplasia, Incontinentia Pigmenti, Fabry Disease, and Congenital Insensitivity to Pain with Anhidrosis-Reference-Cited by-同舟云学术

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Genetic Disorders with Dyshidrosis: Ectodermal Dysplasia, Incontinentia Pigmenti, Fabry Disease, and Congenital Insensitivity to Pain with Anhidrosis

Published:2016 Issue: Volume: Page:42-49
ISSN:1421-5721
Container-title:Perspiration Research
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Author:

Wataya-Kaneda Mari

Publisher

S. Karger AG

Cited by 5 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. A Neonate With a Rash;Pediatrics;2023-06-21

2. The evolution of the initial manifestations and renal involvement of chinese patients with classical and late-onset Fabry disease at different sexes and ages;BMC Nephrology;2023-04-05

3. Global warming, heat-related illnesses, and the dermatologist;International Journal of Women's Dermatology;2021-01

4. Incontinentia pigmenti in adults;American Journal of Medical Genetics Part A;2019-05-22

5. Dyshydrosis and dyshydrotic dermatoses: characteristics of clinical presentation, diagnosis, and treatment;Klinicheskaya dermatologiya i venerologiya;2018

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