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Research 781–810 of 1000+
- Lichen planus pigmentosus and its variants: review and update
- Repigmentation of hair following adalimumab therapy
- Segmented heterochromia in scalp hair
- Becker's Nevus Syndrome
- Multi-dermatomal unilateral nevus comedonicus along the lines of Blaschko: a rare presentation
- Genetics of blond hair
- "Curly" Wood and Tiger Tails
- Hair repigmentation associated with the use of brentuximab
- Evaluation of hair humidity resistance/moisturization from hair elasticity.
- Topically applied tretinoin in the treatment of trichostasis spinulosa
- Overnight loss of pigmented hair in autoimmune autonomic neuropathy treated with IVIg
- Sudden onset hair loss and colour change
- Pili Annulati: A case series and proposal for classification
- Generalized Asymptomatic Cutaneous Pits and Comedones in a Young Woman
- MELATONIN
- Melatonin: functions and ligands
- A randomized double-blind placebo-controlled pilot study to assess the efficacy of a 24-week topical treatment by latanoprost 0.1% on hair growth and pigmentation in healthy volunteers with androgenetic alopecia
- Vitiligo
- Asian Hair: A Review of Structures, Properties, and Distinctive Disorders
- K31 as a novel marker for clear secretory cells in human eccrine sweat glands
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Hair removal using a long-pulsed alexandrite laser.
- A case of severe autoimmune hemolytic anemia after a receipt of a first dose of SARS‐CoV‐2 vaccine
- Lectin‐binding profiles for normal skin appendages and their tumors
- Atrichia and Papular Lesions: Report of a Case
- Segmented Heterochromia in Black Scalp Hair Associated With Iron-Deficiency Anemia
- The role of the adrenal glands in regulating onset of winter fur growth in mink (<i>Mustela vison</i>)
- Melanosis Coli After Long-Term Ingestion of Cape Aloe
- Coexistence of acquired localized hypertrichosis and lipoatrophy after lupus panniculitis
- Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria.