Latest papers

A randomized, single-blind comparison of the efficacy, tolerability and cosmetic acceptance of Propyless or Fenuril treatment of patients with dry skin.

Keratitis-ichthyosis-deafness (KID) syndrome.

[Pruritus and dryness of the skin in chronic kidney insufficiency and dialysis patients - a review].

Granulomatous slack skin presenting as acquired ichthyosis and muscle masses.

Sarcoidosis characterized as acquired ichthyosiform erythroderma.

Sjögren-larsson syndrome: a study of clinical symptoms and dermatological treatment in 34 Swedish patients.

Connexin-26 mutations in deafness and skin disease.

Unique mosaic X/Y translocation/insertion in infant 45,X male.

[Hereditary ichthyosis in Tunisia: epidemiological study of 60 cases].

[Xerosis: a dysfunction of the epidermal barrier].

Defect of hepatocyte growth factor activator inhibitor type 1/serine protease inhibitor, Kunitz type 1 (Hai-1/Spint1) leads to ichthyosis-like condition and abnormal hair development in mice.

CGI-58, the causative gene for Chanarin-Dorfman syndrome, mediates acylation of lysophosphatidic acid.

Granulocytic nuclear differentiation of lamin B receptor–deficient mouse EPRO cells

Mouse neutrophils lacking lamin B-receptor expression exhibit aberrant development and lack critical functional responses

Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype.

Cochlear implantation and connexin expression in the child with keratitis-ichthyosis-deafness syndrome.

Chanarin-Dorfman syndrome caused by a novel splice site mutation in ABHD5.

Clinical and genetic characterization of Chanarin-Dorfman syndrome.

Ichtyose acquise révélant une maladie de Hodgkin. Une nouvelle observation

An update on molecular aspects of the non-syndromic ichthyoses.