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Research 151–180 of 1000+
- Cicatricial Alopecia
- Primary cutaneous follicle center lymphoma presenting as frontal fibrosing alopecia
- Serum level of calprotectin as a new inflammatory marker in patients with alopacia areata
- Non-Invasive Techniques for Evaluating Alopecia Areata
- Dermatopathology Workshop Summary, Berlin 2004
- Lichen Planopilaris and Frontal Fibrosing Alopecia as Model Epithelial Stem Cell Diseases
- Approach to the adult female patient with diffuse nonscarring alopecia
- Regulatory roles of androgens in cutaneous wound healing
- Interventions for female pattern hair loss
- Testosterone target therapy: focus on immune response, controversies and clinical implications in patients with COVID-19 infection
- The clinical spectrum of parathyroid disease
- Advances in Hair Diseases
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Therapeutic Updates on Lichen planopilaris and Frontal Fibrosing Alopecia: A Systematic Review
- Folliculin, the Product of the Birt-Hogg-Dube Tumor Suppressor Gene, Interacts with the Adherens Junction Protein p0071 to Regulate Cell-Cell Adhesion
- Dermoscopic features of follicular mycosis fungoides of nonscalp areas: Report of 11 cases and literature review
- Folliculotropic CD8+ mycosis fungoides associated with diffuse mucosal involvement
- Acrodermatitis Enteropathica: A Case Report Involving a Delayed Diagnosis
- Focal perifollicular mucinosis of the eyelid presenting as a benign nevus
- Subject Index
- Extraction Videodermoscopy of Eruptive Vellus Hair Cyst
- Basal cell carcinoma — molecular biology and potential new therapies
- Zinc deficiency associated with hypothyroidism: An overlooked cause of severe alopecia
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hidradenitis secondary to nirogacestat, a recently approved desmoid tumor medication
- Pruritic Trichostasis Spinulosa: A Rare Variant
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Adnexotropic Variants of the Interface Dermatitides: A Review
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma