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Research 271–300 of 1000+
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- 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
- 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
- When Diet Trends Go Viral: Cutaneous Manifestations of Social Media-Driven Fad Diets and Supplements
- RASopathic Skin Eruptions during Vemurafenib Therapy
- Cronkhite-Canada Syndrome (CCS)—A Rare Case Report
- Erythroderma, Alopecia, Anhidrosis, and Vitiligo as Complications of a Red Ink Tattoo—A Case Report
- Diagnosis and management of tinea infections.
- Utility of dermoscopy in alopecia areata
- Recently Identified Forms of Epidermolysis Bullosa
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- Read-Through for Nonsense Mutations in Type XVII Collagen‒Deficient Junctional Epidermolysis Bullosa
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review
- Linear Alopecia Areata in a 4-year-old Patient: A Rare Clinical Variant
- Alopecia areata during the convalescent phase of kawasaki disease
- A Rare Case of Cronkhite-Canada Syndrome
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development
- Investigating the Genetic Association of Selected Candidate Loci with Alopecia Areata Susceptibility in Jordanian Patients
- Alopecia Universalis Associated with Ulcerative Colitis and The Role of Azathioprine
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Alopecia and Associated Toxic Agents: A Systematic Review
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Alopecia Areata: A Review of the Role of Oxidative Stress, Possible Biomarkers, and Potential Novel Therapeutic Approaches
- Paradise Nut Paradox: Alopecia Due to Selenosis from a Nutritional Therapy
- Skin manifestations associated with systemic diseases – Part I
- Immune therapies for alopecia areata: evidence and new perspectives
- Therapeutic Effect of Superficial Scalp Hypothermia on Chemotherapy-Induced Alopecia in Breast Cancer Survivors
- Dermoscopy and Trichoscopy in Dermatomyositis—A Cross-Sectional Study