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Research 31–60 of 793
- Keratosis follicularis spinulosa decalvans: a family study of seven male cases and six female carriers.
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- A Rare Case of Keratosis Follicularis Spinulosa Decalvans Affecting a Female Child
- Keratosis follicularis spinulosa decalvans in a family
- Topical tacalcitol ointment can be a good therapeutic choice in erythromelanosis follicularis faciei et colli
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Sjogren-Larsson syndrome
- Homoeopathic management of keratosis pilaris with Arsenic Album: A case report
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genetics of Inherited Ichthyoses and Related Diseases
- Primary cicatricial alopecia
- Keratosis follicularis spinulosa decalvans in a female
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Oral Retinoids in Dermatology
- Hair Follicular Expression and Function of Group X Secreted Phospholipase A2 in Mouse Skin
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Primary cicatricial alopecias
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Clinical report of a Holstein's calf with ichthyosis.
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Efficacy and Safety of Long-Pulsed 755-nm Alexandrite Laser for Keratosis Pilaris: A Split-Body Randomized Clinical Trial
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- A rare complication of follicular hair unit extraction: Kaposi’s varicelliform eruption