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Research 781–810 of 1000+
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- Disorders of Keratinization
- Alopecia in Belgian Blue crossbred calves: a case series
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Off-label dermatologic uses of IL-23 inhibitors
- Zebrafish Model of Hereditary Pigmentary Disorders
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Stem-cell therapy in dermatology – Challenges and opportunities
- Hirsutism
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Isolated Linear Discoid Lupus Erythematosus of Scalp Following Lines of Blaschko
- Epidermal mammalian target of rapamycin complex 2 controls lipid synthesis and filaggrin processing in epidermal barrier formation
- Gene-knockout mice with abnormal epidermal and hair follicular development
- 860 Understanding cellular & molecular responses in the treatment of pediatric lymphatic anomalies
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Laminin 332 Is Indispensable for Homeostatic Epidermal Differentiation Programs
- An Approach to Hair Loss in Pediatric Primary Care
- Childhood‐onset systemic lupus erythematosus with trisomy X and the increased risk for bone complications: a case report
- Increased risk of alopecia areata in patients with autism spectrum disorders: A Korean nationwide population-based study
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- The Hair Erector Muscle: Order and Disorder of this Often Forgotten Structure
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- p53 Is a Direct Transcriptional Repressor of Keratin 17: Lessons from a Rat Model of Radiation Dermatitis
- Third International Research Workshop on Alopecia Areata
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
- Tertiary hypothyroidism in a dog
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- RISK FACTORS, PREVALENCE AND DIAGNOSIS OF HUTCHISON GILFORD SYNDROME WITH SPECIAL REFERENCE TO CASE REPORTS