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Research 691–720 of 1000+
- cDNA Cloning, Expression, and Assembly Characteristics of Mouse Keratin 16
- Skin Manifestations Associated with Autoimmune Liver Diseases: a Systematic Review
- Serum level of vitamin D in patients with alopecia areata
- P63 targeted deletion under the FOXN1 promoter disrupts pre-and post-natal thymus development, function and maintenance as well as induces severe hair loss
- Platelet-Rich Plasma (PRP) in Dermatology: Cellular and Molecular Mechanisms of Action
- Confluent and Reticulated Papillomatosis Associated with Polycystic Ovarian Syndrome
- Cyclin-Dependent Kinase 4/6 Inhibitors and Dermatologic Adverse Events: Results from the EADV Task Force “Dermatology for Cancer Patients” International Study
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Culprits of Medication-Induced Telogen Effluvium, Part 1
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Mutations in the helix termination motif of mouse type I IRS keratin genes impair the assembly of keratin intermediate filament
- Alopecia areata susceptibility variant in MHC region impacts expressions of genes contributing to hair keratinization and is involved in hair loss
- Using qualitative methods to establish the clinically meaningful threshold for treatment success in alopecia areata
- Clinical study of twenty-nail dystrophy in Korea
- Twenty-Nail Dystrophy of Alopecia Areata
- Twenty‐nail dystrophy and alopecia areata in an adult male with thymoma‐associated myasthenia gravis: A case report
- Upadacitinib: A New Weapon for the Treatment of Twenty-Nail Dystrophy
- T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy
- Twenty nail dystrophy with alopecia areata in an atopic child
- A generalized reticulate eruption with scarring alopecia, vulvovaginitis, keratoderma, and 20-nail dystrophy in a 70-year-old woman
- Analysis of Skin, Hair and Nail Diseases in the Adults with Beta Thalassemia Major
- Nail lichen planus in a patient with alopecia totalis
- Skin features in myotonic dystrophy type 1: An observational study
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Nail Matrix Pathology in Cronkhite–Canada Syndrome: The First Case Report
- Selenium poisoning from consumption of contaminated wheat: a case series from rural Maharashtra, India
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- [Two cases of the rare Cronkhite-Canada syndrome].
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report