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Research 151–180 of 1000+
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Disease causing homozygous variants in the human hairless gene
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- Androgenetic alopecia: pathogenesis and potential for therapy
- Oral Manifestations of Hematologic and Nutritional Diseases
- Premature graying of hair
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- Trichoscopy in Hair Shaft Disorders
- <i>WNT10A</i> , dermatology and dentistry
- The clinical spectrum of parathyroid disease
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- EMQN best practice guidelines for molecular genetic testing and reporting of 21-hydroxylase deficiency
- Roles of tumor suppressors in regulating tumor-associated inflammation
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- HAIR REGROWTH
- Androgens and hair loss
- Physiology and Medical Treatments for Alopecia
- Male Pattern Baldness
- Comparative Study Between 2% Minoxidil Topical Spray vs. Intradermal Injection (Mesotherapy) for Treatment of Androgenetic Alopecia in Female Patients: A Controlled, 4-month Randomized Trial
- Alopecia and its medical management
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Breakdown of Immune Tolerance in AIRE-Deficient Rats Induces a Severe Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy–like Autoimmune Disease
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- 46,XY DSD due to impaired androgen production
- Molecular basis of hypohidrotic ectodermal dysplasia: an update
- Alopecia areata: An update
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Genetics of Structural Hair Disorders