Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
Migranti trattati come bestie nelle navi Cie, l'Arci presenta un esposto in procura - Redattore Sociale
Medical Science Response of Oral Acitretin in Congenital Icthyosiform Erythroderma: A Case Report.
Autosomal Recessive Congenital Ichthyosis | Actas Dermo-Sifiliográficas
A, Venn diagram showing DEGs comparing ichthyosis subtypes: NS, LI,... | Download Scientific Diagram
A Japanese Case of Ichthyosiform Erythroderma with a Novel Mutation in NIPAL4/Ichthyin | HTML | Acta Dermato-Venereologica
PDF) Congenital lamellar ichthyosis in Tunisia is caused by a founder nonsense mutation in the TGM1 gene | Hamida Turki - Academia.edu
JaypeeDigital | eBook Reader
The Major Orphan Forms of Ichthyosis Are Characterized by Systemic T-Cell Activation and Th-17/Tc-17/Th-22/Tc-22 Polarization in Blood - ScienceDirect
PDF) Prevalence of autosomal recessive congenital ichthyosis: A population-based study using the capture-recapture method in Spain | Antonio Torrelo - Academia.edu
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
A multicenter study on quality of life of the “greater patient” in congenital ichthyoses | Orphanet Journal of Rare Diseases | Full Text
Ichthyosis score (IS) 0 1 2 3 4 Erythema score (ES)
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
Congenital Ichthyosiform Erythroderma (CIE, Non-bullous CIE)
Lamellar Ichthyosis (autosomal recessive congenital ichthyosis, ARCI) - Neurology Advisor
Pleomorphic Ichthyosis: Proposed Name for a Heterogeneous Group of Congenital Ichthyoses with Phenotypic Shifting and Mild Residual Scaling | HTML | Acta Dermato-Venereologica
Photograph shows a 15-year-old CIE male Egyptian patient. | Download Scientific Diagram
Mutations in transglutaminase 1 gene in autosomal recessive congenital ichthyosis in Egyptian families
PDF) Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients | Gitte Strauss - Academia.edu
Study design eligible subjects underwent computerized randomization for... | Download Scientific Diagram
Inherited ichthyoses/generalized Mendelian disorders of cornification | European Journal of Human Genetics
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