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Research 391–420 of 1000+
- ATYPICAL KAWASAKI DISEASE PRESENTING AS TELOGEN EFFLUVIUM IN AN 11 YEAR OLD FEMALE
- Ptosis in childhood
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- Histopathology of non-scarring alopecia
- Neonatal Occipito-Lınear and Temporo-Fronto-Parıetal Alopecıa: Can Non-Marginal and Marginal forms of the Transient Neonatal Hair Loss be Found Together?
- Congenital atrichia and hypotrichosis
- “Case Report : Early Congenital Syphilis”
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Hair Loss in Children
- Interactions of the Vitamin D Receptor with the Corepressor Hairless
- Hair loss in infancy and childhood
- Hair Transplantation Update
- Histopathology of Scarring and Nonscarring Hair Loss
- Platelet-Rich Plasma in the Management of Alopecia: A Systematic Review and Meta-Analysis of Clinical Evidence
- Evaluation of Atherogenic Indexes in Patients With Lichen Planopilaris: A Case-Control Study
- Keratin disorders: from gene to therapy
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Alternative uses of dermoscopy in daily clinical practice: An update
- Hair Loss in Children
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- British Hair and Nail Society
- Cutaneous manifestations of systemic infection in children
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Non-viral delivery of the CRISPR/Cas system: DNA<i>versus</i>RNA<i>versus</i>RNP
- Hair Shafts in Trichoscopy
- 834 Effectiveness of Hemostatic Net in Non-meshed Partial-thickness Skin Grafts
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Unique Dermatological and Systemic Manifestations in a Classic Pediatric Case of Kindler Syndrome: A Case Report and Literature Review