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Research 30 of 819
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- 371 Hair follicles are critical modulators of skin barrier function
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Trichothiodystrophy
- British Society for Paediatric Dermatology Annual Meeting, Sheffield, 18-19 November 2016
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Netherton's syndrome and ichthyosis linearis circumflexa.
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- Exploring the Relationship Between Ichthyosis and Scalp Paresthesia: Potential Connection and Treatment Approach with Fluocinolone
- Ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome treated with acitretin
- Ichthyosis hystrix
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- MULTIPLE DEFECTS OF THE HAIR SHAFT IN NETHERTON'S DISEASE.
- Neonatal ichthyosis-sclerosing cholangitis syndrome caused by a novel CLDN1 mutation: a case report and literature review
- Netherton Syndrome – Responding to Oral Retinoids
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- Ichthyosis Follicularis With Alopecia and Photophobia
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Sjogren-Larsson Syndrome
- Ichthyosis fetalis in a cross‐bred lamb
- Clinical report of a Holstein's calf with ichthyosis.
- Miscellaneous Skin Diseases
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome