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Research 31–60 of 183
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Trichodystrophies: A hair-raising differential diagnosis
- Trichoscopy in Hair Shaft Disorders
- Role of Trichoscopy in Children's Scalp and Hair Disorders
- Inherited Disorders of the Hair
- Autosomal recessive woolly hair syndrome: a series of eight patients in an Indian population
- Hair Loss in Children
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Diagnosis and management of hair loss in children
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- [Black piedra in South Africa. 1st description in a child with bamboo hair, pili torti and congenital erythroderma ichthyosiforme].
- Genetic Susceptibility to Alopecia
- Trichoscopy in Unveiling the Triad of Netherton Syndrome
- Trichoscopy in genetic hair shaft abnormalities
- Hair microscopy: an easy adjunct to diagnosis of systemic diseases in children
- A polarizing light microscopy can be an easy and reliable diagnostic tool of congenital keratinizing disorders including Netherton syndrome
- Recent Approaches in the Treatment of Polycystic Ovary Syndrome: An Update
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Lamellar ichthyosis, dwarfism, mental retardation, and hair shaft abnormalities
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Genetic Hair Disorders: A Review
- Diseases of Periocular Hair
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- AN UPDATE OF HAIR SHAFT DISORDERS
- Hair shaft disorders in children – An update
- Current Genetics in Hair Diseases
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Trichorrhexis Invaginata in Tinea Capitis: A Rare Occurence
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control