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Research 481–510 of 1000+
- Cutaneous signals of immune system disease
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Aesthetic medicine treatments for oncology patients — a narrative literature review
- INVESTIGATING THE MECHANISMS UNDERLYING THE PATHOGENESIS OF ALOPECIA AREATA
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Decision‐Making Regarding the Administration of Live Vaccines to Patients With a <i>FOXN1</i> Heterozygous Missense Variant
- Diseases of Hair and Nails
- Case Report of Wound Treatment with Hyiodine Gel in an Occasional KID Syndrome Patient
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- PRIDE syndrome with lumbosacral hypertrichosis
- Utility of dermoscopy in alopecia areata
- British Association of Dermatologists living guideline for managing people with alopecia areata 2024
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Alopecia universalis during treatment with leflunomide and adalimumab - Case report
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- British Association of Dermatologists living guideline for managing people with alopecia areata 2025
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Dramatic and persistent loss of eyelashes
- Recombinant Thrombomodulin Used to Successfully Treat Cronkhite-Canada Syndrome with Disseminated Intravascular Coagulation due to Sepsis in a Compromised Patient
- Lymphocytes, neuropeptides, and genes involved in alopecia areata
- The Role of Interferon-γ in Autoimmune Polyendocrine Syndrome Type 1
- Recently Identified Forms of Epidermolysis Bullosa
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Keratins: the hair shaft's backbone revealed
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2