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Research 871–900 of 1000+
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Role of Trichoscopy in diagnosing Genotrichosis—A Report of Two Cases
- Tinea favosa: psoriasiform favus in bindi area of an adult
- Acrodermatitis enteropathica – diagnostic challenges
- SAT-358 Hypercalcemia-Induced Altered Mental Status as the Primary Manifestation of Classic Hodgkin Lymphoma
- SAT-LB82 Myxedema as Presenting Feature of Profound Primary Hypothyroidism in a Toddler
- The role of biologic treatment in special scenarios in hidradenitis suppurativa: Facial and nape phenotype, dissecting cellulitis of the scalp, and lymphedema
- Hyperadrenocorticism Associated with Sex Steroid Excess
- Comorbidities in Dermatology
- Clinicopathological features and expression of four keratins (K10, K14, K17 and K19) in six cases of eruptive vellus hair cysts
- Acneiform Rash Caused by an Unlikely Drug: Topiramate
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- A97 TACROLIMUS-ASSOCIATED HEMOLYTIC UREMIC SYNDROME IN A PEDIATRIC LIVER TRANSPLANT RECIPIENT
- Infliximab Induced Lupus in Crohnʼs Disease
- HIV infection mimicking autoimmune disorder
- Dupilumab Associated Progression of Alopecia Areata to Alopecia Universalis: A Case Report
- An Unusual Patchy Alopecia in a 15th Century Altarpiece From Colmar, France
- Evaluation of difficult alopecia areata cases requiring histopathological confirmation
- Unveiling the Effect of Age and IgE Level on Alopecia Areata: Insights from Comparative RNAseq Analysis
- A rare presentation of systemic lupus erythematosus associated with thymoma-induced multiorgan autoimmunity
- Ophiasis Pattern Alopecia Areata in an Infant
- Tinea capitis favosa misdiagnosed as tinea amiantacea
- The use of topical ruxolitinib 1.5% cream in frontal fibrosing alopecia: A case report
- Circumscribed Alopecia: An Unusual Manifestation of Pediculosis Capitis
- Unusual presentation with polymenorrhagia and markedly high 17-hydroxy progesterone levels in a lady with Non-Classic Congenital Adrenal Hyperplasia.
- Systemic Absorption and Pharmacokinetics of Five Novel Topical Dermatologic Agents: A Review
- Laboratory and clinical haemostatic aberrations in primary dermatologic disease: A review
- Case report: Novel p.Val306Met missense mutation in TRPV3 in a case of Olmsted syndrome accompanied by squamous cell carcinoma
- Comprehensive Evaluation of Neuropsychiatric and Mucocutaneous Manifestations in the Diagnosis of Systemic Lupus Erythematosus: A Complete Clinical Approach to a Case
- Multiple ulcerative plaques on the folds