Search
for
Sort by
Research 31–60 of 1000+
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Supplementary Material for: Coexistence of Monilethrix and Androgenetic Alopecia: A Case Report and Review of the Literature
- Monilethrix – Case report of a rare disease
- Masquerading of trichotillomania in a family with monilethrix
- Claves diagnósticas en displasias pilosas II
- Cómo hacer que dos más dos sumen cinco
- Marie-unna hereditary hypotrichosis
- A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance
- Trichorrhexis Invaginata and Netherton’s Syndrome
- Fibrosing alopecia in a pattern distribution in two brothers with pili multigemini
- Alopecia in children
- Hair shaft miniaturization causes stem cell depletion through mechanosensory signals mediated by a Piezo1-calcium-TNF-α axis
- Hair loss in children.
- Keratins: the hair shaft's backbone revealed
- Disorders of hair
- Morphological Approach to Hair Disorders
- Light microscopy of the hair: A simple tool to "untangle" hair disorders
- Hair and nail disorders of childhood
- Hair Disorders
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Congenital atrichia and hypotrichosis
- Improvement in Hair Loss and Better Hair Quality with Vitamin Therapy in Monilethrix
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Manifestations of Systemic Disease
- Informàtica i Dret penal: Els delictes relatius a la informàtica
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Björnstad Syndrome With Late‐Onset Alopecia Mimicking Androgenetic Alopecia: Histopathological and Genetic Findings
- <i>De novo</i> mutations in monilethrix
- Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report
- Trichoscopy in Unveiling the Triad of Netherton Syndrome