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Research 301–330 of 720
- Tufted Hair Folliculitis Decalvans as a Clinical Diagnostic Sign
- Clinico-Epidemiological Study of Scalp Dermatosis at Tertiary Care Centre in Central India
- Evaluation of neutrophil to lymphocyte ratio, platelet to lymphocyte ratio, mean platelet volume, CRP and ESR with disease severity in patients with alopecia areata
- Systemic lupus erythematosus presenting with bullous lesions, cutaneous vasculitis and laryngeal ulcerations-a rare association
- Description of skin lesions
- Aldesleukin
- Hypersensitivity Diseases
- Tufted Folikülit: Bir Olgu Sunumu
- Nonscarring Alopecias
- Main Plenary Sessions: Summaries of Papers
- Eye and skin disease
- Selected topics in pediatric hair loss
- Benefit-Risk Assessment of GLP-1 Receptor Agonists: Implications for Dermatologists and Plastic Surgeons
- Metabolic syndrome and dermatological diseases: association and treatment
- Glucocorticoid-Induced Side Effects Cause Oral Lesions in Systemic Lupus Erythematosus: A Case Report
- Emerging Topical and Systemic JAK Inhibitors in Dermatology
- Recurrent pruritic polymorphic lesions associated with weight loss
- Overexpression of hypoxia-inducible factor-1α in hidradenitis suppurativa: the link between deviated immunity and metabolism
- Madarosis: A marker of many Maladies
- Immunologic adverse reactions of β-blockers and the skin (Review)
- New Frontiers of Non‐Invasive Detection in Scalp and Hair Diseases: A Review of the Application of Novel Detection Techniques
- 1,314
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Sustaining treatment response in alopecia areata through tofacitinib dose tapering: A single-center retrospective study
- Suprabasal Desmoglein 3 Expression in the Epidermis of Transgenic Mice Results in Hyperproliferation and Abnormal Differentiation
- Patterns of desmocollin synthesis in human epithelia: immunolocalization of desmocollins 1 and 3 in special epithelia and in cultured cells.
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Outer root sheath (ORS) cells organize into epidermoid cyst-like spheroids when cultured inside Matrigel: a light-microscopic and immunohistological comparison between human ORS cells and interfollicular keratinocytes
- Identification of Differentially Expressed Genes During a Wool Follicle Growth Cycle Induced by Prolactin