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Research 991–1000 of 1000+
- Erworbene Alopezien im Kindesalter
- Retinoids Putting the “A” in Alopecia
- A Case Report of Cronkhite-Canada Syndrome Complicated by Membranous Nephropathy
- Syndromic epidermolysis bullosa simplex subtype due to mutations in the KLHL24 gene: series of case reports in Russian families
- [Two cases of the rare Cronkhite-Canada syndrome].
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing
- Therapeutic Response of Alopecia Areata‐Associated Nail Changes to Baricitinib
- Identification of a novel homozygous LAMB3 mutation in a Chinese male with junctional epidermolysis bullosa and severe urethra stenosis: A case report