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Research 31–60 of 1000+
- Hidradenitis Suppurativa/Acne Inversa/Dissecting Terminal Hair Folliculitis
- Hirsutism: diagnosis and treatment
- Hair follicles and their role in skin health
- Hair Loss in Children
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Biology and Genetics of Hair
- Genetics of Structural Hair Disorders
- Cantú syndrome with coexisting familial pituitary adenoma
- Female Adolescent Hair Disorders
- Hair Disorders
- Hair loss in infancy and childhood
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- HAIR AND SYSTEMATIC DISEASE
- Expanding the therapeutic landscape of minoxidil for androgenetic alopecia: topical, oral and sublingual formulations
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- The Genetics of Human Skin Disease
- Endocrine Influences on Hair Growth
- Thyroid hormone action on skin.
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Acquired Localized Hypertrichosis Induced by Rivastigmine
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Minoxidil-induced hypertrichosis: Pathophysiology, clinical implications, and therapeutic strategies
- Hypertrichosis Induced by Minoxidil: A Case of Systemic Absorption from Scalp Occlusion
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Novel mutations in the keratin-74 (KRT74) gene underlie autosomal dominant woolly hair/hypotrichosis in Pakistani families
- Madarosis
- Dermatologic manifestations of endocrine disorders