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Research 361–390 of 1000+
- Myotonic Dystrophy—A Progeroid Disease?
- The Wound Reporting in Animal and Human Preclinical Studies (WRAHPS) Guidelines
- Sebaceous gland diseases: clinical picture risk factors and treatment
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Hair follicle-specific keratins and their diseases
- Vitamin D and skin diseases: A review
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Loose Anagen Hair Associated with Wooly Hair Caused by a Heterozygous, Intronic KRT71 Variant
- Oral minoxidil in trichology: A review
- Comparative Study of Some Potential Paracrine Factors Produced by Normal and Androgenetic Alopecia Hair Follicles
- Zinc and Zinc Transporters in Dermatology
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- JAK-Inhibitors Beyond the Label: Emerging Applications in Dermatology
- Development of Woolly Hair and Hairlessness in a CRISPR−Engineered Mutant Mouse Model with KRT71 Mutations
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Gene-knockout mice with abnormal epidermal and hair follicular development
- Key Factors in the Complex and Coordinated Network of Skin Keratinization: Their Significance and Involvement in Common Skin Conditions
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- A rare hair loss in children: Monilethrix
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity