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Research 811–840 of 845
- AB023. An atypical clinical presentation of alopecia in two patients with systemic lupus erythematosus
- Histopathology of Scarring and Nonscarring Hair Loss
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Trichoscopy in alopecia areata and trichotillomania
- 41248 The Impact of Obesity on Confluent and Reticulated Papillomatosis Treatment Outcomes in a Pediatric Cohort
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- A case of familial trichomegaly with synophrys in association with loose anagen syndrome
- Multiple eruptive dermatofibromas in patients with systemic lupus erythematosus treated with prednisone
- Treatment of insulin resistance with tirzepatide leading to improvement of hair loss
- Monilethrix: A rare hereditary condition
- Discreet monilethrix: De novo mutation on the example of polish families
- Dermoscopy of Graham–Little–Piccardi–Lassueur Syndrome
- A retrospective case series: Unique clinical presentation and treatment outcomes of Trichophyton violaceum and soudanense tinea in a pediatric population
- Valproic acid monotherapy induced longitudinal melanonychia
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Unusual Cause of Chronic Diarrhea: Cronkhite-Canada Syndrome
- Monilethrix
- Lipedematous alopecia: an uncommon clinicopathologic variant of nonscarring but permanent alopecia
- Congenital atrichia associated with nevus flammeus: A rare association
- Successful Treatment of Canities Subita with Baricitinib
- “Downy hair sign”—A clue to autoimmune disease in curly hair
- Isolated hair loss on the eyebrow: five cases with trichoscopic features
- Aldosterone- and cortisol-cosecreting adrenal adenoma, ovarian hyperthecosis and breast cancer
- Histopathological change of age-related hearing loss in female advance-aged CBA/CaJ mice
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Diphencyprone Induced Vitiligo: A Case Report
- Novel Androgen Receptor Gene Variant Containing a Premature Termination Codon in a Patient with Androgen Insensitivity Syndrome
- Hair Number per Follicular Unit as a Marker of Treatment Response to Combined Autologous Scalp‐Derived Micrografts and Allogeneic SHED ‐ CM in Male Androgenetic Alopecia