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Research 841–870 of 1000+
- A Combination Flap for Repair of Eclabium
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Autoimmunity: Alopecia Areata
- RASopathic Skin Eruptions during Vemurafenib Therapy
- The mouse keratin 6 isoforms are differentially expressed in the hair follicle, footpad, tongue and activated epidermis
- The burden of alopecia areata: A scoping review focusing on quality of life, mental health and work productivity
- How Biotin Induces Misleading Results in Thyroid Bioassays: Case Series
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- 27th Meeting of the Society of Hair Testing (SoHT)
- Clinicopathologic Case 2: Multiple Intraoral White Lesions in a 55-year-old Female
- K6irs1, K6irs2, K6irs3, and K6irs4 Represent the Inner-Root-Sheath-Specific Type II Epithelial Keratins of the Human Hair Follicle1
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Apoptosis resistance in peripheral blood lymphocytes of alopecia areata patients
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Krt6a-Cre Transgenic Mice Direct LoxP-Mediated Recombination to the Companion Cell Layer of the Hair Follicle and Following Induction by Retinoic Acid to the Interfollicular Epidermis
- Preparing the hair follicle canal for hair shaft emergence
- [Loss of hair due to vitamin A].
- Toxic Side Effects of Targeted Therapies and Immunotherapies Affecting the Skin, Oral Mucosa, Hair, and Nails
- Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- A Novel Epithelial Keratin, hK6irs1, is Expressed Differentially in All Layers of the Inner Root Sheath, Including Specialized Huxley Cells (Flügelzellen) of the Human Hair Follicle
- Inducible deletion of epidermal <i>Dicer</i> and <i>Drosha</i> reveals multiple functions for miRNAs in postnatal skin
- Cutaneous Neuroimmune Interactions in Peripheral Neuropathic Pain States
- Keratins 6, 16, and 17 in Health and Disease: A Summary of Recent Findings
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Trichotillomania in Children
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Comparison of Zn, Cu, and Fe Content in Hair and Serum in Alopecia Areata Patients with Normal Group