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Research 211–240 of 685
- Author Index
- The Rotterdam Study: objectives and design update
- Overexpression of the calcium sensing receptor accelerates epidermal differentiation and permeability barrier formation in vivo
- Madarosis: A marker of many Maladies
- Chilblains in Turkey: a case-control study
- Applications of Plasma-Activated Liquid in the Medical Field
- Semifluorinated Alkanes as New Drug Carriers—An Overview of Potential Medical and Clinical Applications
- Low-Molecular-Weight Synthetic Antioxidants: Classification, Pharmacological Profile, Effectiveness and Trends
- Ocular and Mucocutaneous Sequelae among Survivors of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Togo
- Novel potential therapeutic targets of alopecia areata
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Adaptive Balance in Posterior Cerebellum
- Molecular basis of hypotrichosis with juvenile macular dystrophy in two siblings
- Characterization of<i>CDH3</i>-Related Congenital Hypotrichosis With Juvenile Macular Dystrophy
- Atypical clinical presentation of primary and secondary cutaneous follicle center lymphoma (FCL) on the head characterized by macular lesions
- Homozygous Deletion in CDH3 and Hypotrichosis With Juvenile Macular Dystrophy
- Macular Abnormalities Associated With 5α-Reductase Inhibitor
- Síndrome dos cabelos anágenos frouxos associada à distrofia macular: descrição de uma família
- Hypotrichosis with juvenile macular dystrophy
- An Australian family with macular dystrophy linked to autosomal recessive alopecia universalis
- Macular Alopecia: A Single‐Center Retrospective Cohort Study to Describe an Underrecognized Pattern of Alopecia
- Macular burn secondary to diode laser epilation
- Macular Amyloidosis
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- CDH3 gene related hypotrichosis and juvenile macular dystrophy – A case with a novel mutation
- Hypotrichosis with Juvenile Macular Dystrophy in Saudi Arabia: 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
- Hypotrichosis with juvenile macular dystrophy: a case report with molecular study