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Research 571–600 of 1000+
- A Comprehensive Literature Review of JAK Inhibitors in Treatment of Alopecia Areata
- Sebaceous gland abnormalities in fatty acyl CoA reductase 2 (Far2) null mice result in primary cicatricial alopecia
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- First symposium on natural gene therapy of the skin
- 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
- Mesenchymal Stem Cells for the Treatment of Skin Diseases
- [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
- Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations
- 314 Molecular genetic dissection of ILVEN leads to successful targeted therapy
- Autoimmune polyendocrine syndrome type 1 a case report from Bangladesh
- A patient with diffuse hair loss
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- A randomized, double-blind, placebo- and active-controlled, half-head study to evaluate the effects of platelet-rich plasma on alopecia areata
- Trichothiodystrophy
- The psychology of hair loss and its implications for patient care
- Cutaneous toxicities of cancer therapy
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- A gene for pachyonychia congenita is closely linked to the keratin gene cluster on 17q12-q21.
- Cutaneous Reactions to Chemotherapeutic Agents
- Acquired Zinc Deficiency Dermatosis in Man