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Research 811–840 of 1000+
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Combined activity of selenite-resistant bacteria and Pisum sativum sprout extract against Malassezia furfur: A preliminary qualitative evaluation
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Ayurvedic Approach in Management of Vata-Kaphaja Artavdushti (PCOS)
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- An Atypical Female Case of Ichthyosis Follicularis, Alopecia, and Photophobia (IFAP) Syndrome with Severe Lower Limb Contractures Requiring Orthopedic Surgery
- Prevalence of MMP-1 rs1799750 Polymorphism in Androgenetic Alopecia: A Cross-Sectional Study in an Indonesia Population
- Netherton Syndrome in a 9-Month-Old Child: Unraveling a Complex Dermatologic Disorder
- Atrichia congenita with papular lesions: A rare cause of pediatric alopecia
- Multi-ancestry tandem repeat association study of hair colour using exome-wide sequencing
- The necessity of investigations to clarify sex and racial disparities in pathophysiology of Long COVID
- Pictorial Essay on Hair Loss; the Result of Head Bones Displacement
- Clinical Findings, Response to Steroid Treatment, and Recurrence Rate in Alopecia Areata Patients with or without a Nonsynonymous Variant of Coiled-Coil Alpha-Helical Rod Protein 1
- A rare cause of irrevocable childhood alopecia feigning alopecia universalis: Atrichia congenita with papular lesions
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Study on Changes of 19 Steroids in Plasma From 9 Diagnosed Patients With P450 Oxidoreductase Deficiency
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Inherited Epidermolysis Bullosa: A Clinical Case
- Alopecia Areata in 12 years old female treated with Oral Azathioprine: A case report and review
- WNT10B (wingless-type MMTV integration site family)
- Study of Skin Expression of MicroRNA-146a in Patients with Alopacia Areata
- A study of cutaneous manifestations of systemic lupus erythematosus in Malwa region of India
- Natural Killer Group 2 Type D (NKG2D) Gene Polymorphism in Systemic Lupus Erythematosus-Suez Canal Region - Egypt
- Androgen effects on the skin
- Kennedy's disease and partial androgen insensitivity syndrome. Report of 4 cases and literature review
- Comparative study of efficacy of excimer light therapy vs intralesional triamcinolone vs topical 5% minoxidil: an observational study
- Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I
- Why are men with premature alopecia at higher risk of benign prostatic hyperplasia? And what about prostate cancer?
- BJD Editor's Choice
- Nonclassic Congenital Adrenal Hyperplasia: An Overview