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Research 211–240 of 1000+
- A Neonate with Unexplained Hair Loss
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- Approach to Investigation of Hyperandrogenism in a Postmenopausal Woman
- Hairless: A nuclear receptor corepressor essential for skin function
- N02. Hair and Nails
- Alopezien und Hypotrichosen im Kindesalter
- Clinical Snippets
- Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome
- Bachmann–Bupp syndrome and treatment
- Reply
- Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review
- An Assessment of Quality-of-Life Following Tissue Expansion in Pediatric Patients
- Acne Syndromes and Mosaicism
- Hair loss in infancy and childhood
- Acne and Systemic Diseases
- Polarized microscopy in genetic hair disorders: case series
- Clinical, Laboratory, and Radiological Diagnosis of Hyperandrogenism
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Shared Phenotypes Among Segmental Progeroid Syndromes Suggest Underlying Pathways of Aging
- Hair Disorders
- Index
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Clinical and trichoscopic characteristics of temporal triangular alopecia: A multicenter study
- Alopecia Triangular Temporal. Revisión de las manifestaciones clínicas y Dermatoscópicas.
- Hair and nail disorders of childhood
- Hair loss in infancy and childhood
- 8368 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- 9209 Functional Evaluation Of Novel CYP21A2 Variants: Expanding The Genetic Basis Of Non-classic CAH
- Reply
- A Scandinavian case of skin fragility, alopecia and cardiomyopathy caused by<i>DSP</i>mutations