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Research 211–240 of 1000+
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Congenital atrichia and hypotrichosis
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Hair Shaft Dysplasias
- <i>De novo</i> filament formation by human hair keratins K85 and K35 follows a filament development pattern distinct from cytokeratin filament networks
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Male fertility and skin diseases
- Unruly hair
- A Mutational Hotspot in the 2B Domain of Human Hair Basic Keratin 6 (hHb6) in Monilethrix Patients
- Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Hair loss in children.
- Progeroide Syndrome
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Defining the identity of mouse embryonic dermal fibroblasts
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Secondary cicatricial and other permanent alopecias
- DERMATOLOGIC DISEASES AND PROBLEMS OF WOMEN THROUGHOUT THE LIFE CYCLE
- The Spectrum of Skin Disease Among Indian Children
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Hypotrichosis with juvenile macular dystrophy