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Research 331–360 of 1000+
- Research Snippets
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
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- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Dissection of genetic variation and evidence for pleiotropy in male pattern baldness
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- Commonly associated disorders with complete scalp alopecia in early childhood: A review
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Complex X chromosome rearrangement associated with multiorgan autoimmunity
- Early Diffuse Alopecia in a Neonate with Congenital Syphilis
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Hormone therapy in acne
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- Genetics of Inherited Ichthyoses and Related Diseases
- Keratins and disease at a glance
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- Teratogenic effect of isotretinoin in both fertile females and males (Review)
- Hair loss in children.
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Hemiagenesis of the thyroid gland detected by coincidence—what is the clinical relevance?
- Skin Manifestations in Primary Immunodeficient Children
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases