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Research 421–450 of 1000+
- Successful Management of Folliculitis Decalvans
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Polycystic Ovary Syndrome
- Transforming growth factor-β in stem cells and tissue homeostasis
- Quoi de neuf en recherche dermatologique ?
- National scientific medical meeting 1996 abstracts
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Disorders of Keratinization
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Exploring the Complexities of Atopic Dermatitis: Pathophysiological Mechanisms and Therapeutic Approaches
- A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Werner′s syndrome
- Polymorphisms of the genes ABCG2, SLC22A12 and XDH and their relation with hyperuricemia and hypercholesterolemia in Mexican young adults
- Male androgenetic alopecia
- Keratins and skin disease
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Female Androgenetic (?) Alopecia
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Female pattern alopecia: current perspectives
- Frontal Fibrosing Alopecia in Men: A Review of the Literature
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Severe metabolic disorders coexisting with Werner syndrome: a case report
- Congenital atrichia associated with situs inversus and mesocardia
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome