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Research 571–600 of 1000+
- Multiple Myeloma–Associated Amyloidosis Presenting With Acrolocalized Acquired Cutis Laxa
- Androgenetic Alopecia
- Immunoglobulin E and Serum Interleukin-13 and Bacteria in Patients with Alopecia Areata
- Skin manifestations of hyperandrogenism: an update
- Non-Invasive Techniques for Evaluating Alopecia Areata
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Trachyonychia with juvenile pityriasis rubra pilaris
- Acute Alopecia Associated With Albendazole Toxicosis
- Acute Alopecia Associated With Albendazole Toxicosis
- Resolution of Discoid Lupus Alopecia With Systemic Hydroxychloroquine and Topical Pimecrolimus Combination Therapy
- Hair Repigmentation as a Melanoma Warning Sign
- Trichothiodystrophy without associated neuroectodermal features in two siblings
- Imaging Tools for Noninvasive Hair Assessment
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- New clinico‐genetic classification of trichothiodystrophy
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Differentiation of frontal fibrosing alopecia and Lichen planopilaris on trichoscopy: A comprehensive review
- Dermoscopy and Trichoscopy in Dermatomyositis—A Cross-Sectional Study
- Utility of trichoscopy in comparison to the standard methods for assessing the disease activity, severity, and therapeutic response in alopecia areata
- A review of cutaneous lupus erythematosus: improving outcomes with a multidisciplinary approach
- Case report of novel combination of anthralin and calcipotriene leading to trichologic response in alopecia areata
- Management of acne
- A clinical and histopathological study of cicatricial alopecia
- Cutaneous manifestations of endocrine diseases in children
- The Roles of Keratinocytes in the Initiation, Progression and Maintenance of Hidradenitis Suppurativa
- A systematic review of neutrophilic alopecias of the scalp in the pediatric population
- Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Notch signaling is significantly suppressed in basal cell carcinomas and activation induces basal cell carcinoma cell apoptosis