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Research 31–60 of 1000+
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- The Dark Side of 5α-Reductase Inhibitors' Therapy: Sexual Dysfunction, High Gleason Grade Prostate Cancer and Depression
- Prevalence of Depression and Anxiety in Women with Polycystic Ovary Syndrome (PCOS) and Associated Factors: A Cross-Sectional Study
- Endocrine disorders in Woodhouse-Sakati syndrome: a systematic review of the literature
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- KID Syndrome: Report of a Case and Support for Its Reclassification as an Ectodermal Dysplasia
- A Case of IFAP Syndrome with Severe Atopic Dermatitis
- Isochromosome Mosaic Turner Syndrome: A Case Report
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- The Use of High-Density SNP Array to Map Homozygosity in Consanguineous Families to Efficiently Identify Candidate Genes: Application to Woodhouse-Sakati Syndrome
- Cronkhite-Canada Syndrome: A Case Report and Literature Review of Gastrointestinal Polyposis Syndrome
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Effects of age and sex on the comorbidities of alopecia areata: A cross‐sectional hospital‐based study
- Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- The Genetics of Human Skin Disease
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Deletion of Deoxyribonucleic Acid Binding Domain of the Vitamin D Receptor Abrogates Genomic and Nongenomic Functions of Vitamin D
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Genetic Hair Disorders: A Review
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- P142 – 3046: Encephalocraniocutaneous lipomatosis, a rare neurocutaneous disorder: Report of additional three cases
- AN UPDATE OF HAIR SHAFT DISORDERS
- Depressive Disorder and Dermatological Autoimmune Diseases
- Congenital atrichia with papular lesions
- WNT Signaling in Disease
- Zinc and Zinc Transporters in Dermatology