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Research 511–540 of 1000+
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- The clinical evaluation of hirsutism
- The Use of Micrografts and Minigrafts in the Aesthetic Reconstruction of the Face and Scalp
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Adverse Reactions to Oral Retinoids An Update
- Diagnostic Criteria for Polycystic Ovarian Syndrome
- ‘Black dots’ seen under trichoscopy are not specific for alopecia areata
- Hirsutism: Diagnosis and management
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice
- Genetic hair and nail disorders
- Alternative uses of dermoscopy in daily clinical practice: An update
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Office Diagnosis of Hair Shaft Defects
- FOXN1 deficient nude severe combined immunodeficiency
- Premature Adrenarche
- Cardiovascular risk factors and events in women with androgen excess
- Expanding the Nude SCID/CID Phenotype Associated with FOXN1 Homozygous, Compound Heterozygous, or Heterozygous Mutations
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- What does acne genetics teach us about disease pathogenesis?
- Management of CAH during pregnancy
- A new case of Ambras syndrome associated with a paracentric inversion (8) (q12; q22)
- Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles
- Cholesterol homeostasis: Links to hair follicle biology and hair disorders
- Hair Loss in Children
- Hormone therapy in acne
- Hirsutism in the United Arab Emirates: a hospital study
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses