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- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- 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
- The Roles of EDA2R in Ageing and Disease
- Ectodermal Dysplasia: Variable Expressions
- Research Snippets
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- The Tabby (Ta), Tabby-c (Tac), and Tabby-J (TaJ) Mutations, Chromosome X
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Biology and Genetics of Hair
- Current Genetics in Hair Diseases
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in hypohidrotic ectodermal dysplasia
- Edar Signaling in the Control of Hair Follicle Development
- 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
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Skin Development and Disease: A Molecular Perspective
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses