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Research 361–390 of 1000+
- PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene
- Whitaker syndrome: A case report of autoimmune polyendocrine syndrome type 1 with dilated cardiomyopathy
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients
- Novel <i>RNF113A</i> Variant Underlying X‐Linked Trichothiodystrophy With Presumed Mosaicism in an Unaffected Mother
- Ectodermal Dysplasia: Variable Expressions
- Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates
- Prostaglandin E2 prevents radiotherapy-induced alopecia by attenuating transit amplifying cell apoptosis through promoting G1 arrest
- Bioengineering the Hair Follicle
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Industry updates in advanced therapy medicinal products and regenerative medicine – March 2026
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Hair Shaft Dysplasias
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Pathogenesis and treatment options for chemotherapy‐induced alopecia: a systematic review
- Phototherapy of androgenetic alopecia with low level narrow band 655-nm red light and 780-nm infrared light
- Enhanced Insights into Frontal Fibrosing Alopecia: Advancements in Pathogenesis Understanding and Management Strategies
- Topical sodium valproate-loaded nanospanlastics versus conventional topical steroid therapy in alopecia areata: a randomized controlled study
- Correction of Diffuse Alopecia in Iron Deficiency Anemia
- US clinics marketing unproven and unlicensed adipose-derived autologous stem cell interventions
- Alopecia
- Congenital hair loss disorders: Rare, but not too rare
- Trichoscopy in Hair Shaft Disorders
- Hair loss in children.
- Alopecia Areata
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders