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Research 121–150 of 702
- When hair dig into the brain, JAKi , may help!
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Genome-wide association study of atopic and autoimmune comorbidities in alopecia areata
- Androgenetic Alopecia: An Update on Pathogenesis and Pharmacological Treatment
- Relationship between Serum 25-Hydroxyvitamin D Levels and Hormonal Status in Infertile Women: A Retrospective Study
- Mutations in γ-secretase subunit–encoding PSENEN underlie Dowling-Degos disease associated with acne inversa
- SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT
- <i>WNT10A</i> , dermatology and dentistry
- Diseases of Periocular Hair
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Beyond goosebumps: Does the arrector pili muscle have a role in hair loss?
- Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases
- Tissue resident and follicular Treg cell differentiation is regulated by CRAC channels
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- The Hirsute Woman: Challenges in Evaluation and Management
- Autoimmune polyglandular syndrome type 4 – case report
- Reduced serum brain-derived neurotrophic factor in patients with first onset vitiligo
- Evaluation of Sleep Quality, Restless Legs Syndrome, Anxiety and Depression in Polycystic Ovary Syndrome
- Plasma proteome–driven identification of druggable immune regulators of alopecia areata, validated by transcriptome and single-cell mapping
- Dermatological Manifestations of Celiac Disease: a Literature Review
- An overview of animal models induced by glucocorticoids
- Polycystic ovary syndrome
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome
- The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep
- Trichotillomania in a Male Patient With Depression: A Case Report
- European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity