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Research 61–90 of 826
- Ichthyosis fetalis in a cross‐bred lamb
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Syndromic or non-syndromic congenital ichthyosis? A case report of two brothers with ichthyosis but microphthalmia and blindness in only one brother
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Clinical report of a Holstein's calf with ichthyosis.
- 155 Exploring perceived quality of life in middle- to old-aged patients with inherited ichthyosis: a qualitative study
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- 305 Overlaps between inflammatory dermatoses and ichthyoses: need for novel therapeutic approaches
- Dental Management in a 7-year-old Child with Ichthyosis Vulgaris: A Rare Case Report
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Ichthyosis, atopic dermatitis, and alopecia
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Ichthyoses
- Ichthyosis vulgaris involving the scalp area affected by androgenetic alopecia.
- The Ichthyoses: A Guide to Clinical Diagnosis, Genetic Counseling and Therapy
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Management of congenital ichthyoses: European guidelines of care, part two
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) Syndrome
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Connexin 26 (<i>GJB2</i>) mutations in keratitis–ichthyosis–deafness syndrome presenting with squamous cell carcinoma
- Lamellar ichthyosis with pseudoexon activation in the transglutaminase 1 gene
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Autosomal recessive congenital ichthyosis due to <i>PNPLA1</i> mutation in a golden retriever–poodle cross‐bred dog and the effect of topical therapy
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome