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Research 271–300 of 1000+
- Hair loss and its management in children
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- Ectodysplasin-A2 induces dickkopf 1 expression in human balding dermal papilla cells overexpressing the ectodysplasin A2 receptor
- 1310 Anti-aging effects of retinoid hydroxypinacolone retinoate on skin models
- Detection of a Novel Missense Mutations in Atrichia with Papular Lesions
- Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- The urine as a diagnostic key for a homozygous EGFR mutation
- Telogen effluvium: a review
- Biotin
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- ALOPECIA AREATA-A CLINICAL ANALYSIS
- People’s experiences of eyebrow transplantation: A qualitative study
- Alopecia and Its homoeopathic treatment
- Hoxc13 polyglycine repeat gain-of-function drives mammalian integument evolution by altering targeted genes and interactions
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- The rising burden of alopecia: A review on aetiology, prevalence and role of homoeopathy
- Use of genetics in the prediction of success in male pattern hair loss therapy and mechanistic studies
- Hair shaft disorders
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Facial skin aging: an integrative analysis of genetics, epigenetics, and lifestyle factors
- Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Hair Shaft Fracture in a Young Athlete: A Rare Case Report of Acquired Trichorrhexis Nodosa
- Evaluating the Role of Thyroid Stimulating Hormone and Ferritin Levels with Hair Loss among Patients with COVID-19: Case-Control Study
- Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles
- Distinct tooth regeneration systems deploy a conserved battery of genes
- Uso actual de la vitamina D en dermatología
- Neuroendocrine Controls of Keratin Expression in Human Skin