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Research 121–150 of 1000+
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Keratosis follicularis spinulosa decalvans in a family
- Olmsted Syndrome Caused by a Homozygous Recessive Mutation in TRPV3
- Molecular Genetics of Keratinization Disorders – What’s New About Ichthyosis
- Curly : a new hair defect mutation in the SELH/bc mouse strain
- Treatment of monilethrix with oral minoxidil
- Keratin 71 Mutations: From Water Dogs to Woolly Hair
- Familial Uncombable Hair Syndrome: Ultrastructural Hair Study and Response to Biotin
- Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects
- Pili Annulati: A case series and proposal for classification
- Moniletherix
- 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
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Buschke-Ollendorff syndrome
- Hutchinson-Gilford syndrome: History, causes, phenotype and research advances
- Recurrent missense mutations in the hair keratin gene hHb6 in monilethrix
- 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
- Clouston’s Syndrome-A Case Report
- 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
- <i>De novo</i> mutations in monilethrix
- <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