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Research 301–330 of 1000+
- An early diagnosis of trichorhinophalangeal syndrome type 1: a case report and a review of literature
- Loose anagen syndrome in one identical twin girl
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Effect of Oral Minoxidil on Monilethrix
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Efficacy of Dupilumab in Treating Atopic Dermatitis With Recurrent Eczema Herpeticum in a Patient With DOCK8-Deficiency Hyper-IgE Syndrome: A Case Report
- Discreet monilethrix: De novo mutation on the example of polish families
- A Mouse Model for the Basal Transcription/DNA Repair Syndrome Trichothiodystrophy
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman
- Collagen Involvement in Health, Disease, and Medicine
- Tricholemmoma and tricholemmal carcinoma and Cowden syndrome
- Off-label uses of retinoids in dermatology
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Clouston’s syndrome: a rare case report
- Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Annual Convention in the Time of COVID
- A Forty-Two-Year-Old Male with Multiple Gastrointestinal Polyps, Cutaneous Manifestations, and Nail Dystrophy
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Finasteride
- PTEN Mediates Activation of Core Clock Protein BMAL1 and Accumulation of Epidermal Stem Cells
- Lean Women with Polycystic Ovary Syndrome
- Utilization of Stem Cells in Medicine: A Narrative Review
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- The Non-Cosmetic Dermatological Use of Botulinum Neurotoxin