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Research 181–210 of 184
- Acrodermatitis Enteropathica in an adult: a case report
- Oral Presentations
- TONGUE, RED
- Raising awareness of Demodex mites: a neglected cause of skin disease
- Ichthyosis Follicularis With Alopecia and Photophobia
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Ichthyosis follicularis, alopecia and photophobia (IFAP) syndrome treated with acitretin
- Ichthyosis follicularis with alopecia and photophobia in a mother and daughter
- A Japanese case of ichthyosis follicularis with atrichia and photophobia syndrome with an MBTPS2 mutation
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Ichthyosis follicularis with alopecia and photophobia (IFAP): late diagnosis in 18‐year‐old man
- Ichthyosis follicularis with alopecia and photophobia syndrome with coexisting palmoplantar keratoderma treated with acitretin
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome (IFAP): A Case Report and Review of the Literature
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Inherited ichthyosis: Syndromic forms
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Séquelles cutanéomuqueuses et oculaires des SJS et de Lyell
- Photosensitization Outbreak in Shorthorn Calves in Missouri
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Hypotrichosis with juvenile macular dystrophy
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Letter from Brisbane [Letters to editor]
- Ocular Manifestations in Avitaminosis