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Research 61–90 of 1000+
- Pili Trianguli et Canaliculi Is a Defect of Inner Root Sheath Keratinization
- Central trichoptilosis with onycholysis
- Co-occurrence of monilethrix and Type 1 diabetes mellitus
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V
- Trichoscopy in alopecias: Diagnosis simplified
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Pili annulati with fragility: Electron microscopic findings of a case
- Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82
- Monilethrix in three generations
- Claves diagnósticas en displasias pilosas II
- Transglutaminase 3: The Involvement in Epithelial Differentiation and Cancer
- Overexpression of Sonic Hedgehog suppresses embryonic hair follicle morphogenesis
- Hair and Nail Relationship
- Contemporary Hair Transplantation
- Hair Loss in Children
- Atypical Protein Kinase C Isoform, aPKCλ, Is Essential for Maintaining Hair Follicle Stem Cell Quiescence
- Unruly hair
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR
- Understanding, recognizing, and managing toxicities of targeted anticancer therapies
- Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome
- Hair That Is Difficult to Manage in a Hispanic Girl
- Keratin 17 Expression in the Hard Epithelial Context of the Hair and Nail, and its Relevance for the Pachyonychia Congenita Phenotype
- Trichoscopy and Trichogram
- Acquired curved hair is caused by fusion of multiple hair matrix cells
- Hair in the Wrong Place
- Perspectives of Alopecia behind the Regulation of Foxn1 Gene Exposes the Human Nude Phenotype
- Gene Expression During Drosophila Wing Morphogenesis and Differentiation
- What may be the markers of the male equivalent of polycystic ovary syndrome?