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Research 901–930 of 1000+
- DERMATOLOGICAL CONDITIONS IN TRANSGENDER PATIENTS: A SYSTEMATIC REVIEW
- Evaluation of difficult alopecia areata cases requiring histopathological confirmation
- Dermatologic Manifestations in Patients with Metabolic Syndrome in Brazil
- After Math of COVID Through Eyes of Tricoscopy
- Nevus Sebaceus With Novel HRAS Sequence Variant Mutation Misdiagnosed as Alopecia Areata
- Topikal Retinoidler
- Hair Loss in Children
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- Clinical study on 88 cases of Korean 20-nail dystrophy
- Complex Regional Pain Syndrome Type I : measurements and treatment
- Adipose Tissue‐Derived Exosomes in the Treatment of Lichen Planopilaris: A Case Report
- Homozygous Nonsense Mutation in DSC3 Resulting in Skin Fragility and Hypotrichosis
- Dermoscopic features of follicular mycosis fungoides of nonscalp areas: Report of 11 cases and literature review
- Erosive Lichen Sclerosus—A Clinicopathologic Subtype
- Impaired Hair Follicle Morphogenesis and Cycling with Abnormal Epidermal Differentiation in nackt Mice, a Cathepsin L-Deficient Mutation
- EGFR inhibitor-induced folliculitis decalvans: a case series and management guidelines
- First Symposium of Ichthyosis Experts
- Overexpression of Bcl-2 Protects from Ultraviolet B-Induced Apoptosis but Promotes Hair Follicle Regression and Chemotherapy-Induced Alopecia
- A Spontaneous Deletion within the Desmoglein 3 Extracellular Domain of Mice Results in Hypomorphic Protein Expression, Immunodeficiency, and a Wasting Disease Phenotype
- Sweat Hypersensitivity‐Induced Urticaria and Sebaceous Adenitis in an American Saddlebred
- Efficacy and safety of non‐cross‐linked hyaluronic acid compound in the treatment of keratosis pilaris: A split‐body randomized clinical trial
- Manifestation of pityriasis amiantacea following initiation of minoxidil
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- The molecular basis of human keratin disorders
- A new mutation Rim3 resembling Re den is mapped close to retinoic acid receptor alpha (Rara) gene on mouse Chromosome 11
- Genetic hair and nail disorders
- Isolation and Characterization of a Putative Keratin-Associated Protein Gene Expressed in Embryonic Skin of Mice
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Acne Syndromes and Mosaicism
- Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance.