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Research 451–480 of 1000+
- A REVIEW ON PREVALENCE, CAUSES, AND TREATMENT STRATEGIES OF HAIR FALL AMONG MEN AND WOMEN
- A REVIEW ON PREVALENCE, CAUSES, AND TREATMENT STRATEGIES OF HAIR FALL AMONG MEN AND WOMEN
- Cholecalciferol-grafted hollow mesoporous silica nanoparticles for targeted and sustained caffeine delivery in alopecia therapy
- Gray Patch Tinea Capitis in Two Siblings
- Telogen Effluvium: Potential causes in Iraq
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- All sites but skin cancer incidences analyzed worldwide by sex, age, and skin type over time (1955-2007), advancing age, and UVB dose reveals important carcinogenic drivers
- Effects of calcitriol combined with metformin in the treatment of polycystic ovary syndrome and its influence on serum monocyte chemotactic factor -1
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome
- Receptors in trichology: Hot spots for hair regeneration
- Corrigendum
- 9. Immunology and Genetics
- Las presunciones jurídicas en el ordenamiento jurídico laboral
- Research Snippets
- Murgi: un antiguo puerto romano: un antiguo puerto romano
- Psoriasis del cuero cabelludo etiología, diagnóstico y tratamiento
- Medical Therapies
- Assessment of Serum Vit D and Serum Ferritin in Female Pattern Androgenic Alopecia
- Extrarenal Expression of 25-Hydroxyvitamin D<sub>3</sub>-1α-Hydroxylase<sup>1</sup>
- The skin as an endocrine organ
- Role of -catenin in Epidermal Stem Cell Expansion, Lineage Selection, and Cancer
- Efficacy and safety of topical calcipotriol in management of alopecia areata: A pilot study
- Cardiometabolic Risk Factors in Atorvastatin-Treated Women with Euthyroid Autoimmune Thyroiditis
- Impact of Reducing Obesity in PCOS: Methods and Treatment Outcomes
- The “Bald Mill Hill” Mutation in the Mouse Is Associated with an Abnormal, Mislocalized HR bmh Protein
- Effects of age and sex on the comorbidities of alopecia areata: A cross‐sectional hospital‐based study
- Viva questions from the IJDVL
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- A unique insertion/duplication in the VDR gene that truncates the VDR causing hereditary 1,25-dihydroxyvitamin D-resistant rickets without alopecia
- Cells to Surgery Quiz: December 2017