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Research 871–900 of 1000+
- Connexin mutations in human disease
- Value of dermoscopy for the diagnosis of monilethrix
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Refractory/relapse thrombocytopenia in a patient with Evans' syndrome successfully treated with zanubrutinib
- Deficient anterior pituitary with common variable immune deficiency (DAVID syndrome): a new case and literature reports
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- A frameshift mutation in the TRPS1 gene showing a mild phenotype of trichorhinophalangeal syndrome type 1
- Steroid Responsive Mononeuritis Multiplex in the Cronkhite–Canada Syndrome
- Introduction to JID Symposium Proceedings 52nd Annual Montagna Symposium on the Biology of Skin “Stem Cells in Skin” Held at Snowmass, Colorado, USA, June 13–17, 2003
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Poster presentationsDP11 Bright, eosinophilic intracytoplasmic inclusion bodies: a rare presentation of acquired epidermodysplasia verruciformis with widespread human papillomavirus infection in a transplant recipient
- Poster presentationsSG11 KRT14 pathogenic or likely pathogenic variants beyond epidermolysis bullosa: dermatopathia pigmentosa reticularis
- Animals in Dermatology
- S2608 A Rare Case of Iron Deficiency Anemia: Cronkhite-Canada Syndrome
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1
- Painful thickened skin on the soles of the feet
- Clouston’s syndrome: a rare case report
- Miscellaneous Skin Diseases
- SkIndia Quiz 24: Itchy papules over face
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- 026 Altered Skin Wound Healing in Homeobox Gene Msx-2 Knockout Mice
- Female Androgenetic (?) Alopecia
- Cutaneous and Mucosal Lichen Planus: A Comprehensive Review of Clinical Subtypes, Risk Factors, Diagnosis, and Prognosis
- The Stem Cell Niche in Regenerative Medicine
- PandaOmics: An AI-Driven Platform for Therapeutic Target and Biomarker Discovery
- The Three-Dimensional Human Skin Reconstruct Model: a Tool to Study Normal Skin and Melanoma Progression
- Development of Heritable Melanoma in Transgenic Mice
- The keratin 19 promoter is potent for cell-specific targeting of genes in transgenic mice