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Research 481–510 of 1000+
- A Case Report and a Review of TRAPPC4‐Related TRAPPopathy
- Psoriasis del cuero cabelludo etiología, diagnóstico y tratamiento
- Alopecia Areata - Current and Emerging Therapies
- Clinical and molecular features in a cohort of Middle Eastern patients with epidermolysis bullosa
- An updated review on acne
- Congenital adrenal hyperplasia
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Alopecia Areata Update
- Central centrifugal cicatricial alopecia
- Epidemiological study of prostate cancer (EPICAP): a population-based case–control study in France
- High Frequency of Symptomatic Zinc Deficiency in Infants in Northern Ethiopia
- Acne vulgaris
- The Evaluation and Management of Hirsutism
- Clinical Presentations and Comorbidities of Pediatric Alopecia Areata
- Acquired 11β-hydroxylase Deficiency by Inhaled Etomidate and its Analogues: A Mimic of Congenital Adrenal Hyperplasia
- Vitiligo: A White Patch that Affects the Soul
- A Survey of Women Polycystic Ovarian Disease (PCOD)
- Different Patterns of Lichen Planus in Three Members of One Family
- SILENT PATCHES, LOUD SCIENCE: REVISITING ALOPECIA AREATA
- Chemotherapy-Induced Alopecia by Docetaxel: Prevalence, Treatment and Prevention
- Fractal Pattern in the Premature Graying of Hair: A Case Report
- Risk factors for the development of and outcomes after diagnosis of autoimmune alopecia areata in patients with inflammatory bowel diseases
- Cancer risk in polycystic ovary syndrome patients: Common treatments and future perspectives
- Gene polymorphisms and serum levels of BDNF and CRH in vitiligo patients
- Cells to Surgery Quiz: April 2020
- Taiwanese Dermatological Association consensus on the diagnosis and management of alopecia areata
- Interplay between fibroblast growth factor 9 (FGF9) and CD44 underlies 46,XY disorders of sex development in Kruppel‐like factor 1 (KLF‐1)‐E325K‐associated congenital dyserythropoietic anaemia (CDA‐IV)
- AORTOCAVAL PARAGANGLIOMA IN VON HIPPEL-LINDAU DISEASE
- Clinical, Biochemical and Molecular Characteristics of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review