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Research 61–90 of 1000+
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Acquired Uncombable Hair
- Dermatopathology of Common Hair Problems
- Inherited Disorders of the Hair
- Hereditary, Congenital, and Acquired Alopecias
- An Autosomal Recessive Woolly Hair/Hypotrichosis Case with LIPH Mutation in a Turkish Patient
- Significant Hair Regrowth With 5% Topical Minoxidil in a Child With Marie Unna Hereditary Hypotrichosis Caused by a Recurrent <i>HRURF</i> Variant
- Hypotrichosis 14: novel variants of the LSS gene in five Chinese families and insights from literature review
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Drug Reactions Affecting Hair: Diagnosis
- Minoxidil induced hypertrichosis in a 2 year-old child
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Nutrition and Hair
- Dermatologic manifestations of endocrine disorders
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Understanding and Management of Female Pattern Alopecia
- Dermatologic Reactions to Targeted Therapy
- Efficacy and safety of oral minoxidil in female androgenetic alopecia
- The effects of topical diazoxide on hair follicular growth and physiology of the stumptailed macaque
- Female pattern hair loss in men: A distinct clinical variant of androgenetic alopecia
- An unusual pattern of alopecia areatas
- Skin Ageing in Women: Pathophysiology and Treatment
- Toward Optimal Health: The Experts Respond to Hair Loss in Women
- Eyelash Trichomegaly: Unusual Feature Associated with Systemic Lupus Erythematosus Patient
- General Characteristics of Hair in Eating Disorders
- Biology and Genetics of Hair
- HAIR AND SYSTEMATIC DISEASE
- Hair disorders in patients with cancer