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Research 301–330 of 1000+
- Syphilis: A great imitator
- Clinical Case Notes. Lipoid proteinosis: a rare disorder with pathognomonic lid lesions
- Dermatoscopic findings of syphilitic alopecia
- Clinical Case Notes. Castleman's disease of the lacrimal gland
- Clinical Case Notes. Malignant melanoma in eviscerated eyeball
- Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome
- Unilateral Straight Hair—A Symptom of Acquired Horner's Syndrome in a Neonate
- Contaminants of emerging concern in the fetal environment
- Dermatopathology Workshop Summary, Berlin 2004
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome
- Polycystic ovary syndrome
- Familial aggregation of alopecia areata
- Polycystic Ovary Syndrome, Insulin Resistance, and Obesity: Navigating the Pathophysiologic Labyrinth
- Evaluation and treatment of male and female pattern hair loss
- Diabetes and cardiovascular events in women with polycystic ovary syndrome: a 20-year retrospective cohort study
- KLK5 and KLK7 Ablation Fully Rescues Lethality of Netherton Syndrome-Like Phenotype
- Genome-wide association study identifies a new locus JMJD1C at 10q21 that may influence serum androgen levels in men
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Polycystic Ovary Syndrome: Diagnosis and Treatment
- Telogen Effluvium: A Review
- Receiver operating characteristic analysis of the performance of basal serum hormone profiles for the diagnosis of polycystic ovary syndrome in epidemiological studies
- Ovarian Hypertension: Polycystic Ovary Syndrome
- Polycystic ovary syndrome and insulin-resistant hyperinsulinemia
- Erosive pustular dermatosis of the scalp: Clinical, trichoscopic, and histopathologic features of 20 cases
- Genetic Defects in Human Pericentrin Are Associated With Severe Insulin Resistance and Diabetes
- Diagnosis and Management of Alopecia in Children
- Idiopathic Hirsutism*
- Acquired scalp alopecia. Part I: A review
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family