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Research 721–750 of 1000+
- Efficacy of topical sensitizers in the treatment of alopecia areata
- Characterization and Management of Hedgehog Pathway Inhibitor-Related Adverse Events in Patients With Advanced Basal Cell Carcinoma
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Dupilumab in Inflammatory Skin Diseases: A Systematic Review
- Novel Hairless Mutations in Two Kindreds with Autosomal Recessive Papular Atrichia
- Hirsutism, Normal Androgens and Diagnosis of PCOS
- Characteristics of Androgenetic Alopecia in Asian
- Pathomechanisms of immune-mediated alopecia
- Female pattern alopecia: current perspectives
- The nude gene and the skin
- Quality of life in children and adolescents with alopecia areata—A systematic review
- Evolution of Hair Treatment and Care: Prospects of Nanotube-Based Formulations
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Ichthyosis with confetti: clinics, molecular genetics and management
- Natural Sources of Therapeutic Agents Used in Skin Conditions
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Follicular unit extraction hair transplant.
- Prevention of chemotherapy-induced alopecia in rodent models
- SOCS1 and SOCS3 as key checkpoint molecules in the immune responses associated to skin inflammation and malignant transformation
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- The Role of the Slc39a Family of Zinc Transporters in Zinc Homeostasis in Skin
- Dermatological problems of the puberty
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Advanced Medical Therapies in the Management of Non-Scarring Alopecia: Areata and Androgenic Alopecia
- Anatomy and Physiology of Hair
- Fortnightly review: Cosmetic surgery
- Hair follicle characteristics as early marker of Type 2 Diabetes