CIAS1 Mutation in a Patient with Overlap between Muckle-Wells and Chronic Infantile Neurological Cutaneous and Articular Syndromes

Publisher： Karger

E-ISSN： 1421-9832|206|3|257-259

ISSN： 1018-8665

Source： Dermatology, Vol.206, Iss.3, 2003-04, pp. : 257-259

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Muckle-Wells Syndrome Effectively Treated with Canakinumab: Is the Recommended Dosing Schedule Mandatory?

By  

Dermatology, Vol. 223, Iss. 2, 2011-09 ,pp. : 113-118

Karger

Access to resources Recommend Favorite

Cutaneous Miliary Tuberculosis in a Chronic Kidney Disease Patient

By  

Case Reports in Dermatology, Vol. 6, Iss. 3, 2014-10 ,pp. : 253-257

Karger

Access to resources Recommend Favorite

A Novel Missense Mutation in Fumarate Hydratase in an Italian Patient with a Diffuse Variant of Cutaneous Leiomyomatosis (Reed’s Syndrome)

By  

Dermatology, Vol. 221, Iss. 4, 2010-11 ,pp. : 378-380

Karger

Access to resources Recommend Favorite

Familial Chilblain Lupus – A Monogenic Form of Cutaneous Lupus Erythematosus due to a Heterozygous Mutation in TREX1

By  

Dermatology, Vol. 219, Iss. 2, 2009-05 ,pp. : 162-166

Karger

Access to resources Recommend Favorite

Humoral Response in a Patient with Cutaneous Nocardiosis

By  

Dermatology, Vol. 200, Iss. 1, 2000-02 ,pp. : 78-80

Karger

Access to resources Recommend Favorite