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Research 601–630 of 1000+
- KRT16 wt Allele
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Genomic Organization and Amplification of the Human Keratin 15 and Keratin 19 Genes
- Localized variant of junctional epidermolysis bullosa with R795X mutation
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- The fundamentals of WNT10A
- Acrodermatitis enteropathica – a diagnostic challenge: case report of late-onset, genetically proven disease with normal zinc serum levels
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Symposium Proceedings of the 4th Intercontinental Meeting of Hair Research Societies: “The World of Hair 2004”
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Ocular manifestation in progeria: A case report
- Epilepsy and Neurodegeneration: Clues in the Hair and Blood Vessels!
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Advances in regenerative medicine-based approaches for skin regeneration and rejuvenation
- Clinical features, with video documentation, of the original familial lewy body parkinsonism caused by α‐synuclein triplication (Iowa kindred)
- Pathogenesis and management of TRPV3-related Olmsted syndrome
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Netherton Syndrome With Trichorrhexis Invaginata “Bamboo Hair” Under Dermoscopy: Case Images
- Netherton Syndrome: A Case-Based Review of Diagnosis, Management, and Emerging Treatments.
- The Glucocorticoid Resistance Syndrome. Two Cases of a Novel Pathogenic Variant in the Glucocorticoid Receptor Gene
- Etiopathogenesis of acne
- The L412F variant of Toll-like receptor 3 (TLR3) is associated with cutaneous candidiasis, increased susceptibility to cytomegalovirus, and autoimmunity
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- Red Blood Cells Folate Level in Patients with Alopecia Areata