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Research 31–60 of 1000+
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness
- Hair Anomalies in a 6-Year-Old Girl
- Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome
- A review of genotrichoses and hair pathology associated with inherited skin diseases
- Trichoscopy in Hair Shaft Disorders
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Hair shaft disorders
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II
- When the algorithm fails and experience wins: An extraordinary trichoscopic case
- Prognosis and Management of Congenital Hair Shaft Disorders with Fragility—Part I
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Hair Shaft Dysplasias
- Keratin disorders: from gene to therapy
- Disorders of hair in children
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Clinical Features and Current Therapeutic Approaches to Monilethrix: A Systematic Review
- Monilethrix: a typical case report with microscopic and dermatoscopic findings
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Faculty Opinions recommendation of Autosomal-dominant woolly hair resulting from disruption of keratin 74 (KRT74), a potential determinant of human hair texture.
- Effect of Oral Minoxidil on Monilethrix
- Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture
- Value of dermoscopy for the diagnosis of monilethrix
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Discreet monilethrix: De novo mutation on the example of polish families
- A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle