Congenital Ichthyosiform Erythroderma (CIE, Non-bullous CIE)
PDF) Congenital lamellar ichthyosis in Tunisia is caused by a founder nonsense mutation in the TGM1 gene | Hamida Turki - Academia.edu
A, Venn diagram showing DEGs comparing ichthyosis subtypes: NS, LI,... | Download Scientific Diagram
Molecular epidemiology of non‐syndromic autosomal recessive congenital ichthyosis in a Middle‐Eastern population - Mohamad - 2021 - Experimental Dermatology - Wiley Online Library
Characteristics of the five ARCI patients with TGM1 mutations included... | Download Table
Ichthyosis score (IS) 0 1 2 3 4 Erythema score (ES)
Distinct skin microbiome community structures in congenital ichthyosis - Tham - 2022 - British Journal of Dermatology - Wiley Online Library
Ichthyosis molecular fingerprinting shows profound TH17 skewing and a unique barrier genomic signature. - Abstract - Europe PMC
Neha Singh Vandana Bansal* Tejaswini Patil Kaizad Damania ABSTRACT KEYWORDS INTERNATIONAL JOURNAL OF SCIENTIFIC RESEARCH
Lamellar Ichthyosis Caused by a Previously Unreported Homozygous ALOXE3Mutation in East Asia
ARCI pedigrees. (a) Pedigrees and construction of haplotypes in the... | Download Scientific Diagram
Autosomal Recessive Congenital Ichthyosis | Actas Dermo-Sifiliográficas
Lamellar Ichthyosis (autosomal recessive congenital ichthyosis, ARCI) - Neurology Advisor
Study design eligible subjects underwent computerized randomization for... | Download Scientific Diagram
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) Genotypic and Clinical Spectrum of Self-Improving Collodion Ichthyosis: ALOX12B, ALOXE3, and TGM1 Mutations in Scandinavian Patients | Gitte Strauss - Academia.edu
Autosomal recessive congenital ichthyosis - Altmeyers Encyclopedia - Department Dermatology
Novel CYP4F22 mutations associated with autosomal recessive congenital ichthyosis (ARCI). Study of the CYP4F22 c.1303C>T founder mutation | PLOS ONE
Autosomal Recessive Congenital Ichthyosis in American Bulldogs Is Associated With NIPAL4 (ICHTHYIN) Deficiency - E. A. Mauldin, P. Wang, E. Evans, C. A. Cantner, J. D. Ferracone, K. M. Credille, M. L. Casal, 2015
Targeted Sequence Capture and High-Throughput Sequencing in the Molecular Diagnosis of Ichthyosis and Other Skin Diseases
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
A multicenter study on quality of life of the “greater patient” in congenital ichthyoses | Orphanet Journal of Rare Diseases | Full Text
Inherited ichthyoses/generalized Mendelian disorders of cornification | European Journal of Human Genetics
