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Research 361–390 of 1000+
- Acne Syndromes and Mosaicism
- Expanding the Cutaneous Spectrum of Nicolaides‑Baraitser Syndrome: Eczema and Generalized Hair Loss
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- Hidradenitis suppurativa: A practical review of possible medical treatments based on over 350 hidradenitis patients
- A kindred with mutant IKAROS and autoimmunity
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- Diagnosis and Management of Polycystic Ovary Syndrome (PCOS)
- An open-label prospective observational study of antiandrogen and non-antiandrogen early pharmacological approaches in females with mild-to-moderate COVID-19. The Pre-AndroCoV Female Trial
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Multiple skin tumours in a Doberman Pinscher with colour dilution alopecia
- Post-Acute COVID-19 Sequelae – ‘COVID Long Hauler’
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- LEKTI: Netherton Syndrome and Atopic Dermatitis
- Immunosenescence and inflammaging in Parkinson’s disease: mechanisms and therapeutic prospects
- Clinical Presentation of Polycystic Ovary Syndrome
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- EBS in Children with De Novo Pathogenic Variants Disturbing Krt14
- Pattern hair loss distribution: a novel presentation for alopecia areata
- Ischemic Vaso-occlusive Retinopathy as Initial Presentation in Pediatric Systemic Lupus Erythematosus: A Case Report
- 증례 : 모발의 황 농도 감소를 보인 모발유황이영양증
- Novel de novo pathogenic variant in the <i>ODC1</i> gene in a girl with developmental delay, alopecia, and dysmorphic features
- Congenital Adrenal Hyperplasia
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Autoimmune polyendocrine syndrome type 1: an Italian survey on 158 patients
- Triglycerides, independent of Ferriman Gallwey Score, is a main determinant of free testosterone index in PCOS
- Cutaneous, Cranial, and Skeletal Defects in Children and Adults with Focal Dermal Hypoplasia
- Hypoparathyroidism as the single major component for decades of autoimmune polyglandular syndrome type 1
- A Current Diagnostic and Therapeutic Challenge: Tinea Capitis