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Research 781–810 of 827
- Symptoms: Pruritic Skin Lesions
- Postzygotic Mutations in Beta-Actin Are Associated with Becker’s Nevus and Becker’s Nevus Syndrome
- Multiple eruptive dermatofibromas in patients with systemic lupus erythematosus treated with prednisone
- Clinical response of alopecia, trichorrhexis nodosa, and dry, scaly skin to zinc supplementation
- Two Clinically Unusual Cases of Folliculotropic Mycosis Fungoides: One with and the Other without Syringotropism
- Treatment of insulin resistance with tirzepatide leading to improvement of hair loss
- Monilethrix: A rare hereditary condition
- Hyperpigmentation following Treatment of Frontal Fibrosing Alopecia
- Rare clinical features of the Ellis van Creveld syndrome: A case report and literature review
- An exclusive review of melatonin effects on mammalian melanocytes and melanoma
- Skin changes during pregnancy: A study from Northeast India
- A Case of Alopecia Totalis with Lichen Planus Hypertrophicus Responded Excellently to Oral Tofacitinib-An Observation
- Eruptive vellus hair cysts: An underdiagnosed entity
- Alopecia areata-like presentations with mogamulizumab therapy
- Bilateral nevus comedonicus of the eyelids: An unusual cause of ptosis and ectropion
- Cosmeceuticals in Dermatology
- Multiple congenital smooth muscle hamartoma: A case report
- 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
- SUN-585 A Case of Atypical Myxedema in Hypothyroidism
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- An approach to disorders of pigmentation
- Unusual Cause of Chronic Diarrhea: Cronkhite-Canada Syndrome
- Cell death in the skin
- New clinico‐genetic classification of trichothiodystrophy
- A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Compound Heterozygous Mutations in the Hairless Gene in Atrichia with Papular Lesions
- Making the head: Caspases in life and death
- Assessment, reliability, and validity of trichoscopy in the evaluation of alopecia in women