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Research 961–990 of 1000+
- Metabolic syndrome in Greek women with polycystic ovary syndrome: prevalence, characteristics and associations with body mass index. A prospective controlled study
- Microimaging of hairless rat skin by magnetic resonance at 900 MHz
- An Update on Drug-Induced Pigmentation
- Neuropsychological Assessment in Elderly Men with Benign Prostatic Hyperplasia Treated with Dutasteride
- Drug reaction with eosinophilia and systemic symptoms and severe involvement of digestive tract: description of two cases
- Medical Treatment of Hepatocellular Carcinoma: Any Progress?
- A regulatory perspective on pharmacokinetic/pharmacodynamic modelling
- Adverse cutaneous reactions to chemotherapeutic agents and cytokine therapy
- From gene to therapy in spinal and bulbar muscular atrophy: Are we there yet?
- Kawasaki disease: an update
- What′s new in cicatricial alopecia?
- Characterization and causal investigations of an alopecia syndrome in Australian fur seals (<i>Arctocephalus pusillus doriferus</i>)
- The expression of the gene <i>asebia</i> in the laboratory mouse: 3. Sebaceous glands
- Isoallopregnanolone reduces tic‐like behaviours in the D1 CT ‐7 mouse model of Tourette syndrome
- Lupus erythematosus: considerations about clinical, cutaneous and therapeutic aspects
- Nanoemulsion Vehicles as Carriers for Follicular Delivery of Luteolin
- Prostate-Sparing Effects in Primates of the Potent Androgen 7α-Methyl-19-Nortestosterone: A Potential Alternative to Testosterone for Androgen Replacement and Male Contraception1
- New treatments for rheumatoid arthritis
- Hirsutism in the Adolescent Female
- Levodopa-induced skin disorders in patients with Parkinson disease: a systematic literature review approach
- Isolation and Characterization of a Fetal-Maternal Microchimeric Stem Cell Population in Maternal Hair Follicles Long after Parturition
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Congenital atrichia and hypotrichosis
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Fatal Toxic Epidermal Necrolysis Associated with Minoxidil
- CUTANEOUS T-CELL LYMPHOMA
- Immunomodulators in the treatment of cutaneous lymphoma
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Prevention of Alopecia in Medical and Interventional Chemotherapy Patients
- Clinical Development of Topoisomerase-Interactive Drugs