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Research 781–810 of 1000+
- Secondary Cicatricial and other Permanent Alopecias
- ALOPECIA AREATA IN INFANTS: IS IT UNCOMMON?
- Untersuchungen zur Ursache des generalisierten Haarausfalls bei jungen Kälbern
- VIBRATIONAL SPECTROSCOPIC INVESTIGATION AND MOLECULAR STRUCTURE OF A 5α-REDUCTASE INHIBITOR: FINASTERIDE
- Pustular allergic contact dermatitis caused by fragrances
- Fibroblast bioelectric signaling drives hair growth
- Berardinelli–Seip syndrome
- Semaglutide-Induced Atypical Pustular Drug Eruption: A Case Report
- Iron Deficiency Anemia Pruritus: A Review with Proposed Mechanisms of Action
- Change in dermatology practice during crisis and normalization periods after the COVID-19 pandemic and potential problems awaiting us
- Etoricoxib
- Registrars’ Symposium: Summaries of Papers
- 1377 Exploring the factors to regulate sweating by transcriptome analysis for anhidrosis: Novel role of olfactory receptors on sweating via exposing to β-ionone
- Acquired and inheritedhair disorders
- Case 6
- The analysis of genetics and associated autoimmune diseases in Chinese vitiligo patients
- 미녹시딜 도포후 전신에 발생한 다모증 1 례
- Leflunomide for the treatment of trichodysplasia spinulosa in a liver transplant recipient
- Piggyback‐Acquired Hypertrichosis
- A case report on the effective management of canine demodicosis
- Canine Sertoli cell tumor: anti-Müllerian hormone, inhibin B, and estrone sulphate
- Minoxidil induced hypertrichosis in a 2 year-old child
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Post-Finasteride Adverse Effects in Male Androgenic Alopecia: A Case Report of Vitiligo
- Omeprazole-induced hypertrichosis in two children
- Platelet-Rich Plasma Resultant Cutaneous Nodules on Scalp
- The role of candidate pharmacogenetic variants in determining valproic acid efficacy, toxicity and concentrations in patients with epilepsy
- The scope and use of valproate in epilepsy.
- Extensive Ichthyosiform Sarcoidosis in a Patient With Juvenile Rheumatoid Arthritis
- Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China