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Research 31–60 of 163
- Congenital hair loss disorders: Rare, but not too rare
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- New developments in the molecular treatment of ichthyosis: review of the literature
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Genetic Susceptibility to Alopecia
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Inherited Disorders of the Hair
- Genetics
- Skin, Genetic Defects, and Aging
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- Genetic Hair Disorders: A Review
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- A keratin scaffold regulates epidermal barrier formation, mitochondrial lipid composition, and activity
- Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome
- Abstracts Pt.30
- Successful induction of oral tolerance in Netherton syndrome
- Trichoscopy in Hair Shaft Disorders
- Hair shaft disorders
- Wnt signaling: the good and the bad
- Role of β-Catenin Activation Levels and Fluctuations in Controlling Cell Fate
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Management of congenital ichthyoses: European guidelines of care, part two