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Research 30 of 332
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Desmoglein 4 is regulated by transcription factors implicated in hair shaft differentiation
- Monilethrix: Beaded hair and hypotrichosis in a child
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Diseases of the hair and scalp
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Monilethrix
- Monilethrix in three generations
- Monilethrix
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil
- Alopecia in a 19-Month-Old Boy
- Monilethrix: A case report imaged by trichoscopy, reflectance confocal microscopy and histopathology
- Moniletherix
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- Hair Shaft Disorders
- Keratins: the hair shaft's backbone revealed
- Office Diagnosis of Hair Shaft Defects
- Monilethrix – Case report of a rare disease
- [Monilethrix--rare syndrome of structural hair abnormalities].
- Monilethrix unveiled by initial androgenetic alopecia.
- Hair Loss in Children
- Hair Anomalies in a 6-Year-Old Girl
- Discreet monilethrix: De novo mutation on the example of polish families
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Monilethrix
- Effect of Oral Minoxidil on Monilethrix
- Masquerading of trichotillomania in a family with monilethrix
- 570 DNA dioxygenases Tet1/2/3 control cell differentiation in the hair follicle keratinocytes via modulating the activity of BMP signaling pathway
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- Monilethrix: A rare hereditary condition