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Research 331–360 of 1000+
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Zinc Spray for Treatment of Acrodermatitis Enteropathica: A Case Report
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- PA15 Becker naevus syndrome associated with a mosaic pathogenic variant in <i>ACTB</i>
- 143 Retrospective Look at Cow-Calf Performance in Spring-Calving Dexter Cattle Scored for Winter Hair Shedding Level
- Professor Han Shirong's Dialectical Analysis of the Experience of Treating Spot Baldness
- Ayurvedic Approach to PCOS-A Critical Review
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Quantification of biotin in plasma samples by column switching liquid chromatography – tandem mass spectrometry
- Clinical report of a Holstein's calf with ichthyosis.
- An Investigation Into the Frequency of Use of Traditional and Complementary Medicine in Patients Presenting to the Dermatology Clinic: A Survey Study
- 773 Generation of human hair follicle organoids in vitro and ex vivo by co-culture of primary human hair matrix keratinocytes and dermal papilla fibroblasts
- LB1077 Cutaneous responses to systemic iron: A potential role for epidermal turnover in mammalian iron excretion
- LB1081 Three-dimensional imaging of tight junction-network across multiple layers of human epidermis by array tomography using backscattered electron-mode scanning electron microscopy
- LB1076 Using the frog embryonic epidermis as a model to study desmosome function during development
- 876 Imaging nanoscale changes in desmosome protein organization
- 875 A novel animal model of Desmoglein 1 (Dsg1) deficiency reveals an essential role for Dsg1 in epidermal barrier formation
- 874 Elevated expression of osteopontin splice variants in nonmelanoma skin cancer compared to normal skin and adult keratinocytes
- Effects of an online educational curriculum on knowledge and competence in managing onychomycosis
- Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2
- Hair loss in a 16-year-old girl
- Hypersensitivity Diseases
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- SUMMARIES OF PAPERS
- Pilosebaceous Unit (PSU)
- Hair Today
- Festschrift in honor of the 65th birthday of Dr. Howard I. Maibach
- Scanning Electron Microscopic Study on Collagen Fibrils in the Mink Dermis during the Hair Cycle and Growth