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Research 151–180 of 1000+
- Folliculitis decalvans including tufted folliculitis: clinical, histological and therapeutic findings
- SWEET SYNDROME: AN UNUSUAL PRESENTATION OF CHRONIC GRANULOMATOUS DISEASE IN A CHILD
- [Artículo traducido] Características clínicas y sociodemográficas de la alopecia areata en 5 ciudades colombianas: un análisis del RENAAC
- Evaluation of clinical and lifestyle factors associated with disease severity in adult patients with scalp seborrheic dermatitis
- Protein-Losing Enteropathy as the First Presentation of Systemic Lupus Erythematosus in a Resource-Limited Setting in Sri Lanka: A Case Report
- The Role of Sex and Gender in Dermatology - From Pathogenesis to Clinical Implications
- Cutaneous manifestations of metabolic diseases: uncommon presentations
- Epidemiological, Clinical, and Trichoscopic Features of Syphilitic Alopecia: A Retrospective Analysis and Systematic Review
- Granuloma Annulare Mimicking Alopecia Mucinosa in a Child: An Atypical Presentation
- Isolated Body Hair Loss: An Unusual Presentation of Lichen Planopilaris
- Localized pemphigus vulgaris on scalp: an atypical presentation.
- Folliculitis Decalvans With Frontal Fibrosing Alopecia in a Dark Phototype: Presentation of Folliculitis Decalvans and Lichen Planopilaris Phenotypic Spectrum
- Pattern hair loss distribution: a novel presentation for alopecia areata
- Concurrent hepatitis B and autoimmune hepatitis a rare presentation of acute liver failure: a case report
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- Chinese SLE Treatment and Research group (CSTAR) registry 2009–2019: Major clinical characteristics of Chinese patients with systemic lupus erythematosus
- An Observational Study on Association between Alopecia Areata and Systemic Disorders —A Clinical Correlation
- SUN-376 Isolated DHEA-S Production by an Adrenal Neoplasm: Clinical, Biochemical, and Pathologic Findings
- Approaching fertility in congenital adrenal hyperplasia: exploring P30L mutation-induced 21-hydroxylase deficiency with a presentation between non-classical and simple virilizing phenotypes. A case report
- A rare case of complete Vogt-Koyanagi-Harada disease presenting to a tertiary care hospital in late stage: Clinical features, diagnosis, and management
- Proliferative, lymphocytic, infundibular mural folliculitis and dermatitis with prominent follicular apoptosis and parakeratotic casts in a Labrador retriever: Clinical, histopathological and dermoscopic features and co‐morbidities
- Management of alopecia areata
- Pseudofolliculitis barbae; current treatment options
- Lichen planopilaris epidemiology: a retrospective study of 80 cases
- Common Skin Disorders in Pediatric Skin of Color
- Zinc and the Skin
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- A STUDY OF MUCOCUTANEOUS MANIFESTATIONS IN AUTOIMMUNE CONNECTIVE TISSUE DISORDERS AT TERTIARY CARE CENTRE
- Feline immune-mediated skin disorders: Part 2
- Do There Need to Be Visible Lesions to Diagnose Tinea Capitis?