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Research 91–120 of 1000+
- Dermatologic Reactions to Targeted Therapy
- Niosomes as Carrier in Dermal Drug Delivery
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Scalp, Skull, Orbit, and Maxilla Reconstruction and Hair Transplantation
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Darier Sign: A Historical Note
- Conceptual Basis for Use of Chemotherapeutic Agents and Their Pharmacology
- Clinical pathology in equine dermatology
- Long-term consequences of critical illness
- Drugs that affect autonomic functions or the extrapyramidal system
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- New Insight for Enhanced Topical Targeting of Caffeine for Effective Cellulite Treatment: In Vitro Characterization, Permeation Studies, and Histological Evaluation in Rats
- SUSPECTED CUTANEOUS DRUG TOXICITY IN RHEUMATOID ARTHRITIS—AN EVALUATION
- Skin Diseases in Horses
- Significance of iron status in hair loss in women
- Hypertrichosis of the pinnae in a patient using panitumumab
- Abstracts Pt.30
- Interrelation of immunity and tissue repair or regeneration
- Niosomes as a propitious carrier for topical drug delivery
- HAIR AND SYSTEMATIC DISEASE
- Platelet-rich plasma, the ultimate secret for youthful skin elixir and hair growth triggering
- Recent studies on the delivery of hydrophilic drugs in nanoparticulate systems
- Kin‐cohort analysis of <i>LRRK2</i>‐G2019S penetrance in Parkinson's disease
- A preliminary study of finasteride in Tourette syndrome
- Desferrioxamine treatment of aceruloplasminemia: Long‐term follow‐up
- Therapeutic Applications of Nanoemulsion Based Drug Delivery Systems: A Review of Patents in Last Two Decades
- The Clinical Presentation of Systemic Lupus Erythematosus
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements