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Research 211–240 of 1000+
- Ectodermal Dysplasia: Otolaryngologic Manifestations and Management
- Genetic Mapping Of Hereditary Ectodermal Dysplasias And Hair Loss Genes
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Ectodermal Dysplasia: Variable Expressions
- Research Snippets
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- A new type of pachyonychia congenita.
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- 1426 Deletion of hoxc13 in frogs reveals key steps in the molecular evolution of cornified skin appendages
- Connexin mutations in human disease
- Bloch-Sulzberger Syndrome: A Rare X-Linked Dominant Genetic Disorder in a Newborn
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Next-generation Sequencing Identified a Novel EDA Mutation in a Chinese Pedigree of Hypohidrotic Ectodermal Dysplasia with Hyperplasia of the Sebaceous Glands
- Tissue expansion for correction of alopecia in a child with hypohidrotic ectodermal dysplasia
- Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin
- 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
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- Comparative genomics analyses of alpha-keratins reveal insights into evolutionary adaptation of marine mammals
- Unruly hair
- Sebaceous carcinoma arising at a chronic candidiasis skin lesion of a patient with keratitis-ichthyosis-deafness (KID) syndrome