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Research 841–870 of 1000+
- Diagnosis and Management of Polycystic Ovary Syndrome in Adolescent Girls
- Clinicoepidemiological Observational Study of Acquired Alopecias in Females Correlating with Anemia and Thyroid Function
- The Dermatology Life Quality Index (DLQI) used as the benchmark in validation of 101 quality‐of‐life instruments: A systematic review
- Platelet-rich plasma: The journey so far !
- A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report
- Telogen Effluvium
- A review of environmental and health effects of synthetic cosmetics
- Skin cancer: understanding the journey of transformation from conventional to advanced treatment approaches
- The role of dermocosmetics in the management of cancer-related skin toxicities: international expert consensus
- Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes
- The importance of basonuclin 2 in adult mice and its relation to basonuclin 1
- Exploring the reality of exosomes in dermatology
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Male and female pattern hair loss: Treatable and worth treating
- Protease activity, localization and inhibition in the human hair follicle
- A pair of transmembrane receptors essential for the retention and pigmentation of hair
- Training requirements and recommendation for the specialty of dermatology and venereology <i>European Standards of Postgraduate Medical Specialist Training</i>
- Recent advances in preparation and biomedical applications of keratin based biomaterials
- Medical aesthetics – Current trends and a review of its applications
- Time-course RNA-seq analysis reveals stage-specific and melatonin-triggered gene expression patterns during the hair follicle growth cycle in Capra hircus
- Tissue Mechanics in Haired Murine Skin: Potential Implications for Skin Aging
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Game Changers: Blockbuster Small-Molecule Drugs Approved by the FDA in 2024
- A Gender Hypothesis of sex disparities in adverse drug events
- Trichotillomania: What Do We Know So Far?
- Alopecia in a Viable Phospholipase C Delta 1 and Phospholipase C Delta 3 Double Mutant
- Evaluation of quality of life scores and family impact scales in pediatric patients with alopecia areata: a cross‐sectional cohort study
- ChatGPT in medicine: Evaluating psoriasis patient concerns
- Adverse Events in Isotretinoin Therapy: A Single-Arm Meta-Analysis