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Research 661–690 of 1000+
- Loose anagen hair syndrome
- Diet in dermatology: Revisited
- Evaluation of the effects of COVID‐19 pandemic on hair diseases through a web‐based questionnaire
- 5-Alpha reductase deficiency
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Current evaluation of amenorrhea
- Surrogate end-points or primary outcomes in clinical trials in women with polycystic ovary syndrome?
- Epidemiology of hirsutism among women of reproductive age in the community: a simplified scoring system
- Prevalence of Polycystic Ovary Syndrome in Girls Aged 14–18 Years in Isfahan, Iran
- De novo single-nucleotide and copy number variation in discordant monozygotic twins reveals disease-related genes
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Pregnancy and the Skin
- Understanding the role of prostaglandin E2 in regulating human platelet activity in health and disease
- Differential Diagnosis of Hyperandrogenism in Women with Polycystic Ovary Syndrome
- Therapeutic potential of bimatoprost for the treatment of eyebrow hypotrichosis
- The risk of coronary heart disease in men with androgenetic alopecia
- The Clinical Presentation of Systemic Lupus Erythematosus
- Madarosis
- Dermatoses of pregnancy
- Guidelines of care for superficial mycotic infectionsof the skin: Tinea capitis and tinea barbae
- Acquired Progressive Kinking of Hair
- Organ Specificity in Autoimmune Diseases: Thyroid and Islet Autoimmunity in Alopecia Areata
- Patients with specific skin disorders who are affected by COVID ‐19: What do experiences say about management strategies? A systematic review
- Characterization of X-Linked SNP genotypic variation in globally distributed human populations
- The Effect of 5 -Reductase Inhibitors on Erectile Function
- Carriers of 21-Hydroxylase Deficiency Are Not at Increased Risk for Hyperandrogenism*
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Hair loss in elderly women
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern