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Research 211–240 of 1000+
- Follicular Unit Excision in Hair Restoration Surgery
- Hairdressing Practices and Alopecia among Women Aged 15 to 45 in Bamako
- Research Snippets
- Moniletherix
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Novel <i>KRT83</i> and <i>KRT86</i> mutations associated with monilethrix
- Biochemical features of primary cells from a pediatric patient with a gain-of-function <i>ODC1</i> genetic mutation
- Pili Annulati: A case series and proposal for classification
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Syndrome of Birt–Hogg–Dubé, a Histopathological Pitfall With Similarities to Tuberous Sclerosis
- Birt–Hogg–Dubé syndrome
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Buschke-Ollendorff syndrome
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- <i>Malassezia</i> and the Asian menopausal skin
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- Hereditary mucoepithelial dysplasia: unique histopathological findings in skin lesions
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Reversible Myopathy and Ophthalmoparesis After Low-Dose Finasteride Administration for Androgenic Alopecia
- Clouston’s Syndrome-A Case Report
- <i>De novo</i> mutations in monilethrix
- Economic Issues in the Treatment of BPH
- <i>TRPS1</i> mutation associated with trichorhinophalangeal syndrome type 1 with 15 supernumerary teeth, hypoplastic mandibular condyles with slender condylar necks and unique hair morphology
- Two mouse mutations mapped to chromosome 11 with differing morphologies but similar progressive inflammatory alopecia
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Pattern Baldness: Its Genetics Revisited