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Research 361–390 of 1000+
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins
- CPC14 Blaschko-linear trichoepitheliomas: unveiling type 1 segmental mosaicism
- Hypotrichosis and Hair Loss on the Occipital Scalp
- Hypotrichosis in a child with olmsted syndrome
- Ductal breast cancer in a male patient
- Nonclassic Congenital Adrenal Hyperplasia: An Overview
- Main Plenary Sessions: Summaries of Papers
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Molecular Mechanisms Regulating Hair Follicle Development
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- HRT for women with premature ovarian insufficiency: a comprehensive review
- Ectodysplasin research—Where to next?
- Homozygous Dominant Missense Mutation in Keratin 17 Leads to Alopecia in Addition to Severe Pachyonychia Congenita
- The G60S Connexin43 Mutant Regulates Hair Growth and Hair Fiber Morphology in a Mouse Model of Human Oculodentodigital Dysplasia
- Molecular Analysis of a Series of Israeli Families with Comèl-Netherton Syndrome
- Clinical and Genetic Characterization of Tunisian Children with Hereditary 1,25-Dihydroxyvitamin D-Resistant Rickets
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Vitiligo – Study In view of familial occurence
- Successful Management of Netherton Syndrome Using IVIG and Dupilumab: A Case Report
- Multiple facial atrophic scars in childhood
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- Two females with hair loss
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Letter from Brisbane [Letters to editor]
- Clinical Snippets
- Molecular epidemiology of hypospadias: Review of genetic and environmental risk factors
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study