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Research 361–390 of 1000+
- Topical minoxidil and tretinoin combined with an oral vitamin D analog as a treatment for woolly hair
- Acquired progressive kinking of the hair in a Korean female adolescent
- Oral Presentations
- Poly(rC) binding protein 2 acts as a negative regulator of IRES-mediated translation of Hr mRNA
- Alopecia totalis in an infant
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Telogen Effluvium, Diagnosis and Management: A Narrative Review
- Finasteride and Dutasteride in the Treatment of Androgenetic Alopecia: Risk or Benefit?
- Treatment of hereditary hypotrichosis simplex of the scalp with oral minoxidil and growth factors
- Clinical and Molecular Diagnostic Criteria of Congenital Atrichia with Papular Lesions11This paper originally appeared in issue 117:1662–1665, 2001. Following publication the authors indicated that important corrections at page proof were not taken in. To ensure that the paper is published as intended, the editors have decided to reproduce the contents in full.
- A novel missense mutation (C622G) in the zinc‐finger domain of the human hairless gene associated with congenital atrichia with papular lesions
- Preoperative Botulinum Toxin Injection Does Not Improve Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- The Impact of Botulinum Toxin on Hair Transplantation Outcomes: A Split-scalp Randomized Controlled Trial
- Dermatological alterations induced by gynecological hormonal imbalances: Acne, hirsutism and alopecia
- Wanted, dead and alive: Why a multidisciplinary approach is needed to unlock hair treatment potential
- Hirsutism and virilization
- LB1672 Senescent melanocytes in nevus skin stimulate hair growth
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Inherited ichthyoses/generalized Mendelian disorders of cornification
- A clinical case of familial alopecia areata in combination with immune pathology
- Alopecia
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Epidemiological and Trichoscopic Study of Patchy Scalp Alopecia in Children in Delta Egypt
- Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex