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Research 751–780 of 1000+
- Lesions in the Axilla After Hair Removal Using Intense Pulsed Light
- The Associations of Androgen-Related Genes CYP21A2 and CYP19A1 with Severe Acne Vulgaris in Patients from Southwest China
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Expression patterns of hair-related keratins and epithelial keratins in onychopapilloma: The significance of clarifying the origin of onychopapilloma
- Acute Hair Loss 3 Years after Bone Marrow Transplant
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- Carcinogenesis of the Human Scalp. An Immunometabolic Centered View
- Madarosis and facial keratinaceous spines
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- Resolution of Discoid Lupus Alopecia With Systemic Hydroxychloroquine and Topical Pimecrolimus Combination Therapy
- Frontal fibrosing alopecia
- Dissecting Cellulitis of the Scalp: Linking Pathogenesis to Therapy
- Ponatinib-induced pityriasis rubra pilaris-like adnexal dysmaturation: A case report
- British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology
- Lichen Planopilaris: Retrospective Study and Stepwise Therapeutic Approach
- Acne Keloidalis Nuchae
- Congenital atrichia associated with situs inversus and mesocardia
- The <i>Girl with a Pearl Earring</i> : A dermatological puzzle
- Manifestation of pityriasis amiantacea following initiation of minoxidil
- Fundamental research on the action mechanism of the 800 nm semiconductor laser on skin blackheads and coarse pores
- Comorbidities in primary cicatricial alopecia: a systematic review and meta-analysis
- Frequency of Types of Alopecia in a Single-centre Hair Referral Clinic Over a Ten Years Period
- Cutaneous manifestations of endocrine diseases in children
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Adnexotropic Variants of the Interface Dermatitides: A Review
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients