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Research 391–420 of 1000+
- Alopecia Areata Update
- Hair loss and its management in children
- The urine as a diagnostic key for a homozygous EGFR mutation
- Hair loss in infancy and childhood
- Diagnostic challenges in determining alopecia areata
- Diagnosis of hyperandrogenism: clinical criteria
- Androgens in women
- Idiopathic Hirsutism*
- Acquired scalp alopecia. Part II: A review
- Hair Biology
- The Evaluation and Management of Hirsutism
- Chapter 20. Pathogenesis and Treatment of Alopecias
- Acne in Dark Skin
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- The genetically programmed hair growth cycle and alopecia: what is there to know?
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Alopecia Areata
- Melanocytes and Vitiligo (and Hair Graying)
- Pathogenesis and causes of hirsutism
- Subject Index
- Ethnopharmacology and hair: Indian perspectives
- The impact of obesity on the folliculosebaceous unit
- Disruption of P2RY5, an orphan G protein–coupled receptor, underlies autosomal recessive woolly hair
- A conditional multi-trait sequence GWAS discovers pleiotropic candidate genes and variants for sheep wool, skin wrinkle and breech cover traits
- Independent DSG4 frameshift variants in cats with hair shaft dystrophy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A Homozygous Frameshift Mutation in the<i>HOXC13</i>Gene Underlies Pure Hair and Nail Ectodermal Dysplasia in a Syrian Family
- Integrated miRNA-mRNA analysis reveals regulatory pathways underlying the curly fleece trait in Chinese tan sheep
- Altered hair root gene expression profiles highlight calcium signaling and lipid metabolism pathways to be associated with curly hair initiation and maintenance in Mangalitza pigs
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia