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Research 271–300 of 1000+
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Neonatal Ichthyosis and Sclerosing Cholangitis Syndrome
- Hashimoto Thyroiditis - A Comprehensive Review
- Oral Retinoids in Dermatology
- Montagna Symposium 2017—Precision Dermatology: Next Generation Prevention, Diagnosis, and Treatment
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- Beyond the usual: a case of acrodermatitis enteropathica clinically resembling erythrokeratoderma variabilis
- Molecular studies of Hutchinson-Gilford progeria syndrome
- Cells to Surgery Quiz: April 2020
- Urticaria, Drug Hypersensitivity Rashes, Nodules and Tumors, and Atrophic Diseases
- AN OVERVIEW ON POLYCYSTIC OVARIAN SYNDROME
- GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Multiple pigmentierte Basaliome im Capillitium bei Myotonia dystrophia Curschmann-Steinert
- Contents
- Hairy tale of signaling in hair follicle development and cycling
- Loose Anagen Syndrome: A Retrospective Chart Review of 37 Cases
- Mutations in Homocysteine Metabolism Genes Increase Keratin <i>N</i>-Homocysteinylation and Damage in Mice
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Review of the Latest Methods of Epidermolysis Bullosa and Other Chronic Wounds Treatment Including BIOOPA Dressing
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Biotinidase Deficiency: Prevalence, Impact And Management Strategies.
- Long-term expansion and differentiation of adult murine epidermal stem cells in 3D organoid cultures
- Werner's syndrome: incidental finding during pregnancy
- A case of eruptive lichen spinulosus after toxic epidermal necrolysis