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Research 61–90 of 1000+
- Coexisting trichorrhexis nodosa and pili annulati: a case report of hair shaft abnormalities in a syrian family
- Monilethrix in three generations
- Central Centrifugal Cicatricial Alopecia (CCCA)
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases
- Hypotrichosis in a child with olmsted syndrome
- Woolly Hair in Two Siblings
- Acquired and inheritedhair disorders
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- HAIR AND SYSTEMATIC DISEASE
- Proteome Analysis of Human Hair Shaft
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Hair Shaft Dysplasias
- Bamboo Hair Syndrome or Netherton Syndrome - A Case Report
- Netherton Syndrome – Responding to Oral Retinoids
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Effect of Oral Minoxidil on Monilethrix
- Monilethrix with Acitretin
- Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Dermatoscopy of hair shaft disorders
- Genetics of Structural Hair Disorders
- Trichoscopy in Hair Shaft Disorders
- Discreet monilethrix: De novo mutation on the example of polish families
- [Monilethrix is a hereditary hair shaft disorder].
- Hair shaft disorders in children – An update
- Hair physiology and its disorders
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics