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Research 271–300 of 1000+
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- Hair growth promoting effects of adipose tissue-derived stem cells
- Six SNPs and a TTG indel in sheep desmoglein 4 gene are in complete linkage disequilibrium
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Decades of progressive red and yellow nodules
- Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype
- <i>WNT10A</i> , dermatology and dentistry
- White piedra caused by <i>Trichosporon inkin</i> : a report of two cases in a northern climate
- Disease causing homozygous variants in the human hairless gene
- Hairless controls hair fate decision via Wnt/β–catenin signaling
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings
- Hair and Nail Relationship
- Evaluation of Hair Loss
- Diseases of the Hair and Nails
- Abstracts
- Association of Trichorhinophalangeal Syndrome and Loose Anagen Syndrome: A Case Report
- CLINICAL UPDATES IN HAIR
- Abstracts Pt.30
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Hair Shaft Dysplasias
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Hirsutism: Diagnosis and management
- Pseudoacromegaly induced by the long-term use of minoxidil
- Alopecia and Hirsuties
- Hyperandrogenism in polycystic ovary syndrome and adrenal hyperplasia: finding differences to make a specific diagnosis