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Research 61–90 of 1000+
- Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder
- Pili Annulati: A case series and proposal for classification
- Moniletherix
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Keratosis follicularis spinulosa decalvans in a family
- Mutations in KLHL24 Add to the Molecular Heterogeneity of Epidermolysis Bullosa Simplex
- <i>De novo</i> mutations in monilethrix
- Treatment of monilethrix with oral minoxidil
- Hair Anomalies in a 6-Year-Old Girl
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Monilethrix: Beaded hair and hypotrichosis in a child
- 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
- Buschke-Ollendorff syndrome
- Clouston’s Syndrome-A Case Report
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- A missense mutation in the type II hair keratin hHb3 is associated with monilethrix
- A newborn presenting with congenital blistering
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- 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
- Hair That Is Difficult to Manage in a Hispanic Girl
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Loose anagen syndrome in one identical twin girl.
- <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
- Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association
- Polycystic ovarian disease in adult and perimenopausal women