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Research 301–330 of 1000+
- Structural abnormalities of the hair shaft
- Hypertrichosis
- Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings
- RBPJ Mutations Identified in Two Families Affected by Adams-Oliver Syndrome
- Female Pseudohermaphroditism Caused by a Novel Homozygous Missense Mutation of the GR Gene
- Critical Developmental Periods for Effects on Male Rat Genitalia Induced by Finasteride, a 5α-Reductase Inhibitor
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Acne as a chronic systemic disease
- 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
- Hairless is a nuclear receptor corepressor essential for skin function
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- What does acne genetics teach us about disease pathogenesis?