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Research 541–570 of 1000+
- Evolution of long scalp hair in humans
- The Carcinogenesis of the Human Scalp: An Immunometabolic-Centered View
- Epidemiological and Trichoscopic Study of Patchy Scalp Alopecia in Children in Delta Egypt
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Racial and Gender Influences on Skin Disease
- May AMH levels distinguish LOCAH from PCOS among hirsute women?
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- SAT-210 When Acne, Hirsutism and Menstrual Irregularities Are More Than PCOS
- Isolated Linear Discoid Lupus Erythematosus of Scalp Following Lines of Blaschko
- 52993 Regulatory γδ T cells protect human scalp hair follicles from alopecia areata in vivo
- Beyond the Epidermal-Melanin-Unit: The Human Scalp Anagen Hair Bulb Is Home to Multiple Melanocyte Subpopulations of Variable Melanogenic Capacity
- Analysis of the expression pattern of the carrier protein transthyretin and its receptor megalin in the human scalp skin and hair follicles: hair cycle-associated changes
- Treatment of Alopecia in Children
- A Neonate with Unexplained Hair Loss
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- Analysis of hair loss in young adults- A clinical study
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Painful thickened skin on the soles of the feet
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Hair diseases: a big problem on a small surface
- Fibroblast bioelectric signaling drives hair growth