A5025055061- Hair Growth and Disorders
- Dermatologic Treatments and Research
- Genetic and rare skin diseases.
- Autoimmune Bullous Skin Diseases
- Autoimmune and Inflammatory Disorders
- Amyloidosis: Diagnosis, Treatment, Outcomes
- melanin and skin pigmentation
- Medicine and Dermatology Studies History
- RNA regulation and disease
- Body Contouring and Surgery
- Nail Diseases and Treatments
- Cancer and Skin Lesions
- Tracheal and airway disorders
- Parathyroid Disorders and Treatments
- Eosinophilic Disorders and Syndromes
- Skin Protection and Aging
- Esophageal and GI Pathology
- Skin and Cellular Biology Research
- Dermatological and Skeletal Disorders
- Acne and Rosacea Treatments and Effects
- Hypertrophic osteoarthropathy and related conditions
- Whipple's Disease and Interleukins
- Diphtheria, Corynebacterium, and Tetanus
- Intensive Care Unit Cognitive Disorders
- Neuroendocrine Tumor Research Advances
Wake Forest University
2022-2025
Clínica Alemana
2016-2025
Universidad del Desarrollo
2016-2025
Hospital del Salvador
2016-2024
Rutgers, The State University of New Jersey
2024
Capital Health Medical Center Hopewell
2024
Atrium Health Wake Forest Baptist
2022-2023
Hospital Clínico de la Universidad de Chile
2010
University of Chile
2008-2010
Pontificia Universidad Católica de Chile
2010
The frequency of different types alopecia is not clearly reported in recent studies.To analyze the patients consulting at specialist hair clinics (SHC) and to assess for global variations.Multicenter retrospective study including data from evaluated referral SHC Europe, America, Africa Australia.A total 2,835 (72.7% females 27.3% males) with 3,133 diagnoses were included (73% non-cicatricial 27% cicatricial alopecias). In all, 57 characterized. most frequent type was androgenetic (AGA)...
This Patient Page describes the symptoms, diagnosis, and treatment of traction alopecia.
Material and Methods: We conducted a retrospective, multicenter study. Public centers of the Chilean Monoclonal Gammopathies Cooperative Group were asked to search for patients with AL amyloidosis in their databases. Epidemiological, clinical laboratory characteristics evaluated.
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