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Research 121–150 of 1000+
- An updated review of the sebaceous gland and its role in health and diseases Part 2: Pathophysiological clinical disorders of sebaceous glands
- Breast Cancer-Related Neoplastic Alopecia: A Case Report and Review of the Literature
- Unusual Clinical Presentation of a Primary Cutaneous Follicle Center Lymphoma on the Scalp of a Middle-Aged Female: Case Report and Review of the Literature
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Virilization beyond menopause: an uncommon ovarian tumor in an elderly patient with multimodality imaging and pathologic correlation
- A rare case of chronic genian fistula with oral mucosal hair follicle inclusion: case report and review of the literature
- Histopathological Diagnosis of Alopecia Clinically Relevant to Alopecia Areata
- Cirmcumscribed juvenile pityriasis rubra pilaris in a 5-year-old-girl treated with topical keratolytic and steroid
- Circumferential acute limited exanthematous pustulosis
- Dermatopathology Workshop Summary, Berlin 2004
- A clinical and histopathological study of cicatricial alopecia
- Hair and Scalp Changes in Cutaneous and Systemic Lupus Erythematosus
- Perda pilosa por líquen plano pilar após transplante capilar: relato de dois casos e revisão da literatura
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Genetic Variants and Protective Immunity against SARS-CoV-2
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- Dermatological Manifestations of COVID-19: A Brief Review
- Traction alopecia: the root of the problem
- A case of antilaminin 332 mucous membrane pemphigoid showing a blister on the bulbar conjunctiva and a unique epitope on the α3 subunit
- rs4541843 G > A variant near miR-182 is associated with susceptibility, severity, and increased hsa-miR-182-5p expression in alopecia areata
- Alopecia por diluição da cor em uma cadela Staffordshire Bull Terrier azul: Relato de caso
- Cutaneous lupus erythematosus. Diagnostic and therapeutic recommendations of the Polish Dermatological Society
- Oral Presentations
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Nonalcoholic fatty liver disease and polycystic ovary syndrome
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- 461 Identification of a Novel Pathogenic XPC:c.2420+1G>C Variant in a Patient with Xeroderma Pigmentosum
- Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- GENOTYPE ? PHENOTYPE CORRELATIONS IN CUTANEOUS MELANOMA PATIENTS CARRIER OF THE MITF p.E318K PATHOGENIC VARIANT