Search
for
Sort by
Research 121–150 of 1000+
- Acne Syndromes and Mosaicism
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Skin Development and Disease: A Molecular Perspective
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Trichoscopy in Hair Shaft Disorders
- Hair shaft structures in EDAR induced ectodermal dysplasia
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Comparison of comedolytic effect of benzoyl peroxide and adapalene in rhino mice
- Molecular Genetics of Alopecias
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- The clinicopathological spectrum of trichoepitheliomas: a retrospective descriptive study
- Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle
- Oral Manifestations of Hematologic and Nutritional Diseases
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- 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
- Oral Presentations
- Skin Manifestations in Primary Immunodeficient Children
- Morphological Approach to Hair Disorders
- Disease causing homozygous variants in the human hairless gene
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Normal Hair Growth in Children
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Treatment of Hair Loss