Keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with congenital deaf-mutism-Reference-Cited by-同舟云学术

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Keratoderma hereditarium mutilans (Vohwinkel's syndrome) associated with congenital deaf-mutism

Published:2006-07-29 Issue:4 Volume:132 Page:617-620
ISSN:0007-0963
Container-title:British Journal of Dermatology
language:en
Short-container-title:

Author:

PERIS K.,SALVATI E.F.,TORLONE G.,CHIMENTI S.

Publisher

Wiley

Subject

Dermatology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2133.1995.tb08721.x/fullpdf

Reference30 articles.

1. Versuch einer Klinisch-genetischen Klassifikation der hereditarien Palmoplantarkartosen unter Berucksichtigung assoziierter Symptome;Franceschetti;Dermatologica,1960

2. Keratoma hereditarium mutilans;Vohwinkel;Arch Dermatol Syphil,1929

3. Cheratodermia congenita mutilante;Cavalieri;Cronache I.D.I.,1962

4. Hereditary keratodermia and ainhum;Piers;Br J Dermatol,1967

5. Syndrome de Vohwinkel (étude de quatre cas);Sierra;Ann Dermatol Syphil,1975

Cited by 18 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. Pseudoainhum in a patient with tuberous sclerosis complex: a case report and review of the literature;International Journal of Dermatology;2013-07-24

2. Disorders of keratinization;McKee's Pathology of the Skin;2012

3. 9 Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010

4. Disorders of epidermal maturation and keratinization;Weedon's Skin Pathology;2010

5. Connexin-26 mutations in deafness and skin disease;Expert Reviews in Molecular Medicine;2009-11

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