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Research 361–390 of 1000+
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- 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
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Clinical relevance of hair microscopy in alopecia
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Alternative uses of dermoscopy in daily clinical practice: An update
- Hair Loss in Children
- Secondary cicatricial and other permanent alopecias
- A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome
- British Hair and Nail Society
- Hair loss in infancy and childhood
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Hair Loss in Children
- Adams–Oliver syndrome: new evidence in variable expressivity?
- Cutaneous manifestations of systemic infection in children
- 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
- Generalized trichoepitheliomas with alopecia and myasthenia gravis: Clinicopathologic and immunohistochemical study and comparison with classic and desmoplastic trichoepithelioma
- Pioneers in Dermatology and Venereology: An Interview with Professor Danilo V. Stevanovic
- Painful thickened skin on the soles of the feet
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Ptosis in childhood
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Trichoscopy in hair disorders in darker skin: An approach to diagnosis
- A new heterozygous frameshift variant in keratin 10 resulting in ichthyosis hystrix in a father and daughter
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Hair and Nail Relationship