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Research 30 of 66
- Monilethrix: an ultrastructural study
- What Syndrome Is This?
- NEW YORK DERMATOLOGICAL SOCIETY
- Monilethrix: the use of tricoscopy in clinical diagnosis
- Mutation analysis of the typeIIhair keratin gene in a family of Han nationality with monilethrix
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Congenital hair loss disorders: Rare, but not too rare
- Hair Loss in Children
- Hair Shaft Dysplasias
- Advances in Hair Diseases
- Inherited Disorders of the Hair
- Biology and Genetics of Hair
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- AN UPDATE OF HAIR SHAFT DISORDERS
- Monilethrix: A Novel Mutation (Glu402Lys) in the Helix Termination Motif and the First Causative Mutation (Asn114Asp) in the Helix Initiation Motif of the Type II Hair Keratin hHb6
- Genetic Hair Disorders: A Review
- Current Genetics in Hair Diseases
- A mutation in the type II hair keratin KRT86 gene in a Han family with monilethrix
- Telocytes in human skin – are they involved in skin regeneration?
- Diseases of Hair
- Diseases of Hair
- Dermatological Manifestations of COVID-19: A Brief Review
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- Monilethrix in pattern distribution in siblings: Diagnosis by trichoscopy
- Monilethrix in three generations
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players
- Gene detection in a family with monilethrix and treatment with 5% topical minoxidil