Disease: Erythrokeratodermia variabilis ichthyosis
- A Connexin Gene (<em>GJB3</em>) Mutation in a Chinese Family With Erythrokeratodermia Variabilis, Ichthyosis and Nonsyndromic Hearing Loss: Case Report and Mutations Update
- A Connexin Gene (GJB3) Mutation in a Chinese Family With Erythrokeratodermia Variabilis, Ichthyosis and Nonsyndromic Hearing Loss: Case Report and Mutations Update
- A new, recurrent mutation of GJB3 (Cx31) in erythrokeratodermia variabilis
- A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis
- A p.478I>T KRT1 mutation in a case of annular epidermolytic ichthyosis
- Acitretin for erythrokeratodermia variabilis in a 9-year-old girl
- An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22
- Annular Epidermolytic Ichthyosis Mimicking Greither Disease: A Case Report and Literature Review
- Annular epidermolytic ichthyosis: a case report and literature review
- Erythrokeratodermia figurata variabilis
- Erythrokeratodermia variabilis - variant with circumscribed variable erythema and periorificial fixed Bazex Dupre erythema
- Erythrokeratodermia variabilis with adult onset: report of a sporadic case unresponsive to systemic retinoids
- Erythrokeratodermia variabilis with erythema gyratum repens-like lesions
- Erythrokeratodermia Variabilis-like Phenotype in Patients Carrying ABCA12 Mutations
- Erythrokeratodermia variabilis. An enzyme histochemical and ultrastructural study
- Erythrokeratodermia variabilis. Report of three cases and review of the literature
- Expanding the clinical phenotype associated with ELOVL4 mutation: study of a large French-Canadian family with autosomal dominant spinocerebellar ataxia and erythrokeratodermia
- Expanding the clinical phenotype associated with NIPAL4 mutation: Study of a Tunisian consanguineous family with erythrokeratodermia variabilis-Like Autosomal Recessive Congenital Ichthyosis
- Further evidence for localization of the gene of erythrokeratodermia variabilis
- Genetic heterogeneity in erythrokeratodermia variabilis: novel mutations in the connexin gene GJB4 (Cx30.3) and genotype-phenotype correlations
- Genetic linkage between erythrokeratodermia variabilis and Rh locus
- Ichthyosis: etiology, diagnosis, and management
- Netherton syndrome in a Bulgarian patient : Presentation of a case and an update of therapeutic options
- Partial Loss of Function ABCA12 Mutations Generate Reduced Deposition of Glucosyl-Ceramide, Leading to Patchy Ichthyosis and Erythrodermia Resembling Erythrokeratodermia Variabilis et Progressiva (EKVP)
- Recessive mosaicism in ABCA12 causes blaschkoid congenital ichthyosiform erythroderma
- Reticular erythrokeratoderma: a new disorder of cornification
- Retinoids in disorders of keratinization: their use in adults
- The Complex and Critical Role of Glycine 12 (G12) in Beta-Connexins of Human Skin
- Treatment of erythrokeratodermia variabilis with oral synthetic retinoids