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Research 991–1000 of 1000+
- Autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) due to AIRET16M mutation in a consanguineous Greek girl
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: A Case Report
- Twenty-Nail Dystrophy Treated with Hydroxychloroquine in a Patient with Alopecia Areata
- Twenty‐nail dystrophy and alopecia areata in an adult male with thymoma‐associated myasthenia gravis: A case report
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Upadacitinib: A New Weapon for the Treatment of Twenty-Nail Dystrophy
- Overcoming genetic drivers in alopecia areata: hair regrowth in a patient with <i>AIRE</i> gene mutation (autoimmune polyendocrinopathy–candidiasis–ectodermal dystrophy, APECED syndrome) treated with ruxolitinib
- Characterisation of Myotonic Dystrophy type I cell models and drug evaluation by a cell- based quantification platform.