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Research 151–180 of 1000+
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Dermatological Maifestations of Obesity
- Ichthyosis
- Oral Retinoids in Dermatology
- Ichthyosis with confetti: clinics, molecular genetics and management
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Trichothiodystrophy with Dysmyelination and Central Osteosclerosis
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Uso actual de la vitamina D en dermatología
- PHILADELPHIA DERMATOLOGICAL SOCIETY
- Prevalence and associated factors of skin diseases in aged nursing home residents: a multicentre prevalence study
- Controversies in off‐label prescriptions in dermatology: the perspective of the patient, the physician, and the pharmaceutical companies
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis
- Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs
- Analysis of the abnormal human hair keratins by two-dimensional polyacrylamide gel electrophoresis
- Identification of Novel Mutations in Basic Hair Keratins hHb1 and hHb6 in Monilethrix: Implications for Protein Structure and Clinical Phenotype
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Novel association of trichothiodystrophy with autoimmune thyroiditis and autoimmune hemolytic anemia: A case report
- Commentary: Darier-White Disease
- The epidermis: rising to the surface
- Keratin gene mutations in disorders of human skin and its appendages
- Ulerythema ophryogenes with multiple congenital anomalies
- Genetic disorders of keratin: are scarring alopecias a sub-set?
- Large Intragenic KRT1 Deletion Underlying Atypical Autosomal Dominant Keratinopathic Ichthyosis
- Contribution of Environmental Constituents in the Genomic Disruption of Cytokeratins