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Research 21
- Characterization of X‐linked hypohidrotic ectodermal dysplasia (XL‐HED) hair and sweat gland phenotypes using phototrichogram analysis and live confocal imaging
- Significant Correction of Disease after Postnatal Administration of Recombinant Ectodysplasin A in Canine X-Linked Ectodermal Dysplasia
- Genotype-phenotype correlation in boys with X-linked hypohidrotic ectodermal dysplasia
- Ectodysplasin research—Where to next?
- A novel EDA variant that causes X-linked hypohidrotic ectodermal dysplasia in a Chinese family
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Unraveling the Link Between Ectodermal Disorders and Primary Immunodeficiencies
- Darier Sign: A Historical Note
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- An Interesting Case of X-linked Hypohidrotic Ectodermal Dysplasia
- The role of hair follicles and Edar signalling in cutaneous wound healing
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Coordinating the Sculptors: Ectodysplasin-A (EDA) Signaling Cross-Talk with Skeletogenic Pathways
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- Genetic Hair Disorders: A Review
- Skin Development and Disease: A Molecular Perspective
- Transcriptome Profiling and Differential Gene Expression in Canine Microdissected Anagen and Telogen Hair Follicles and Interfollicular Epidermis
- Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
- Patients' Illness Perception as a Tool to Improve Individual Disease Management in Primary Cutaneous Lymphomas
- Ectodysplasin A (EDA) Signaling: From Skin Appendage to Multiple Diseases
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia