Proposal for a 6-step approach for differential diagnosis of neonatal erythroderma
Hereditary palmoplantar keratoderma – phenotypes and mutations in 64 patients
Meta-Analysis of Mutations in ALOX12B or ALOXE3 Identified in a Large Cohort of 224 Patients
Correction to: Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses
Treatment of hereditary palmoplantar keratoderma: a review by analysis of the literature
Phenotypic Variability with SLURP1 Mutations and Diffuse Palmoplantar Keratoderma
Genetical, clinical, and functional analysis of a large international cohort of patients with autosomal recessive congenital ichthyosis due to mutations in NIPAL4
Burden of itch in ichthyosis: a multicentre study in 94 patients
Italian translation, cultural adaptation, and pilot testing of a questionnaire to assess family burden in inherited ichthyoses
Alitretinoin in punctate palmoplantar keratoderma
Alitretinoin reduces erythema in inherited ichthyosis
Hereditary palmoplantar keratodermas. Part II: syndromic palmoplantar keratodermas – Diagnostic algorithm and principles of therapy
Hereditary palmoplantar keratodermas. Part I. Non-syndromic palmoplantar keratodermas: classification, clinical and genetic features
