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Research 61–90 of 1000+
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Interplay between EDA-EDAR and WNT signalling pathways in the development of skin appendages in 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
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- WNT10A mutation causes ectodermal dysplasia by impairing progenitor cell proliferation and KLF4-mediated differentiation
- Alopecia areata in a patient with WNT10A heterozygous ectodermal dysplasia
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- Increased risk of chronic fatigue and hair loss following COVID-19 in individuals with hypohidrotic ectodermal dysplasia
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia
- Hypohidrotic Ectodermal Dysplasia with c.28delG Mutation in Ectodysplasin A Gene and Severe Atopic Dermatitis Treated Successfully with Tofacitinib
- X-linked Recessive Ectodysplasin A Mutations Induced Hypohidrotic Ectodermal Dysplasia and Severe Atopic Dermatitis Successfully Treated with Dupilumab
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Novel missense mutation in the EDA gene in a family affected by oligodontia
- Hair loss among a group of Egyptian children
- Hair and Nail Relationship
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Congenital Atrichia: A Case Report
- N02. Hair and Nails
- Novel splicing‐site mutation in <i>DCAF17</i> gene causing Woodhouse‐Sakati syndrome in a large consanguineous family
- Keratin disorders: from gene to therapy
- The role of P-cadherin in skin biology and skin pathology: lessons from the hair follicle
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Dysfunction of keratinocyte adhesion
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder