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Research 271–300 of 1000+
- Electrophoretic variability in human hair: Comparative sodium dodecyl sulfate‐polyacrylamide gel electrophoresis of body and head hair proteins
- Hair Whorls in the Dog (<i>Canis familiaris</i>). I. Distribution
- A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome
- Pili Annulati: A case series and proposal for classification
- Microneedling radiofrequency in cosmetic dermatology and aesthetics
- Graham–Little–Piccardi–Lassueur syndrome: case report and systematic review of a rare LPP variant
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Cross-Sectional Study Of The Association Between Skin Tags And Vascular Risk Factors In A Bariatric Clinic-Based Cohort Of Irish Adults With Morbid Obesity
- Prematüre Pubarş Olgularının Değerlendirilmesi: Tek Merkez Deneyimi
- A case report of Graham-Little–Piccardi–Lassueur syndrome
- Expression of mRNA for androgen receptor, 5alpha-reductase and 17beta-hydroxysteroid dehydrogenase in human dermal papilla cells
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Radiofrequency Microneedling: A Comprehensive and Critical Review
- Mechanism of action of androgen in hair follicles
- Mucocutaneous manifestations of acquired hypoparathyroidism: An observational study
- DIAGNOSIS AND MANAGEMENT OF HIRSUTISM
- Frontal fibrosing alopecia: a review of eleven patients
- Viewpoint 6
- A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2
- Effectiveness of Radiofrequency Microneedling in the Treatment of Dermatological Conditions: A Systematic Review
- ALOPÉCIA CICATRICIAL E SÍNDROME RARA: DESAFIOS DIAGNÓSTICOS EM DERMATOLOGIA NA ATENÇÃO PRIMÁRIA À SAÚDE
- A Rare association of Mauriac syndrome and Van-Wyk Grumbach syndrome found in a young Saudi girl with poorly controlled type 1 Diabetes and Hypothyroidism: A Case Report and Brief literature review
- Diseases of the Hair
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- An Adult With Hair Loss! a Rare Case of Non-Classical 3β Hydroxysteroid Dehydrogenase (3β HSD) Deficiency
- SAT-134 Postmenopausal Virilization: Rare Case of an Ovarian Tumor Not Easily Identified on Imaging
- Autoimmune polyglandular syndrome type 4 – case report
- Long-lasting Antimicrobial Effect Achieved via Immobilization of Antimicrobial Agents on Hair Shaft
- Peer Review #2 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"
- Peer Review #1 of "Human hair shaft proteomic profiling: individual differences, site specificity and cuticle analysis (v0.1)"