Search
for
Sort by
Research 31–60 of 95
- Hair shaft disorders
- The human keratins: biology and pathology
- <i>Hoxc13</i> mutant mice lack external hair
- Keratin disorders: from gene to therapy
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Biology and Genetics of Hair
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair and Nail Relationship
- Clinical relevance of hair microscopy in alopecia
- Molecular Genetics of Alopecias
- Advances in Hair Diseases
- Woolly Antics between the Sheaths
- Common genetic hair shaft abnormalities may be visualized by light and electron microscope
- Hair Loss in Children
- Disorders of hair in children
- Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin?
- An Autosomal Recessive Form of Monilethrix Is Caused by Mutations in DSG4: Clinical Overlap with Localized Autosomal Recessive Hypotrichosis
- A Variable Monilethrix Phenotype Associated With a Novel Mutation, Glu402Lys, in the Helix Termination Motif of the Type II Hair Keratin hHb1
- Monilethrix Treated with Minoxidil
- Dermoscopy: A rapid bedside tool to assess monilethrix
- Androgen Regulation of the Human Hair Follicle: The Type I Hair Keratin hHa7 Is a Direct Target Gene in Trichocytes
- Hair Keratins and Hair Follicle–Specific Epithelial Keratins
- Hair keratin pattern in human hair follicles grown <i>in vitro</i>
- Monilethrix: A rare hereditary condition
- Monilethrix, a rare inherited hair shaft disorder in siblings
- Monilethrix
- [Studies on monilethrix].
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Hair Anomalies in a 6-Year-Old Girl