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Research 841–870 of 1000+
- TREATMENT OF VALPROATE‐INDUCED HYPERAMMONEMIA
- Trichosporon asteroides: A novel ethiological agent of Kerion celsi in a child
- Proliferating Hybrid Follicular Tumor
- ANAIS DO I CONGRESSO MÉDICO DE FORMOSA- COMEF
- Book Reviews
- ABHRS Results Announced
- Skin shedding and tissue regeneration in African spiny mice (Acomys)
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Content of Citrulline and Other Amino-Acids in a Protein of Hair Follicles
- Spermidine Promotes Human Hair Growth and Is a Novel Modulator of Human Epithelial Stem Cell Functions
- Hepatotoxicity Complicating Flutamide Treatment of Hirsutism
- Complete Structure of an Epithelial Keratin Dimer: Implications for Intermediate Filament Assembly
- Woolly hair nevus
- Acute inflammatory demyelinating polyneuropathy associated with pegylated interferon α 2a therapy for chronic hepatitis C virus infection
- Syphilitic alopecia: uncommon trichoscopic findings
- Structure of human steroid 5α-reductase 2 with the anti-androgen drug finasteride
- Large-scale cultivation of transplantable dermal papilla cellular aggregates using microfabricated PDMS arrays
- <i>Malassezia slooffiae</i>‐associated dermatitis in a goat
- Alopecia neoplastica caused by desmoplastic melanoma
- Overdose of<i>Rogaine</i>®<i>Extra Strength for Men</i>Topical Minoxidil Preparation
- Cronkhite-Canada Syndrome Associated with Serrated Adenoma and Malignant Polyp: A Case Report and a Literature Review of 13 Cronkhite-Canada Syndrome Cases in Korea
- Cronkhite-Canada syndrome: Report of an unusual case
- Differential proteomics of lesional vs. non-lesional biopsies revealed non-immune mechanisms of alopecia areata
- Persistently curly hair phenotype with the use of nivolumab for squamous cell lung cancer
- Demonstration of Inherent Electromagnetic Energy Emanating from Isolated Human Hairs.
- Alopecia associated with quetiapine
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Pachyonychia Congenita-Associated Alopecia. A Microscopic Analysis Using Transverse Section Technique
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica