Search
for
Sort by
Research 991–1000 of 1000+
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Construction of the coexpression network involved in the pathogenesis of thyroid eye disease via bioinformatics analysis
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- The Silent Syndrome of Long COVID and Gaps in Scientific Knowledge: A Narrative Review
- Evolution, classification, structure, and functional diversification of steroid 5α-reductase family in eukaryotes
- Polycystic Ovary Syndrome and Oxidative Stress—From Bench to Bedside
- Treatment options and emotional well-being in patients with rosacea: An unsupervised machine learning analysis of over 200,000 posts
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis