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Research 661–690 of 1000+
- A Case Report of Werner’s Syndrome With a Novel Mutation From India
- Clinical experience on follicular unit extraction megasession for severe androgenetic alopecia
- 1310 Anti-aging effects of retinoid hydroxypinacolone retinoate on skin models
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Glycolytic Dysfunction in Granulosa Cells and Its Contribution to Metabolic Dysfunction in Polycystic Ovary Syndrome
- Microneedles as a perspective for transdermal therapeutic systems
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Hypothyroidism in Dogs
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- THE PEDIATRICIAN AND THE SEXUALLY ACTIVE ADOLESCENT
- The urine as a diagnostic key for a homozygous EGFR mutation
- Complementary evolution of coding and noncoding sequence underlies mammalian hairlessness
- Telogen effluvium: a review
- Inconsolable Crying in Infants: Differential Diagnosis in the Pediatric Emergency Department
- The Relationship between Lichen Planus and Carotid Intima Media Thickness.
- Spatial variation and associated genes of total hair follicle density in goats
- Diagnosis and treatment of polycystic ovarian syndrome: an update
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- 1313 Fzd2 controls multiple aspects of epidermal development through distinct signaling mechanisms
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- People’s experiences of eyebrow transplantation: A qualitative study
- Alopecia and Its homoeopathic treatment
- Dendrobium officinale polysaccharide improves hair regrowth in androgenetic alopecia mice and is associated with coordinated changes in local steroid metabolism, ESR1 activation, and keratin-related follicular responses
- <i>Ashtanindita</i> <i>Purusha</i> – The Clinical Revelation : A Review
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Long-Term Efficacy and Safety of Ritlecitinib in Adults and Adolescents with Alopecia Areata: 3-Year Results from the ALLEGRO Phase 2b/3 and ALLEGRO-LT Phase 3 Clinical Studies