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Research 31–60 of 788
- TONGUE, RED
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Subject Index
- Medical aesthetics – Current trends and a review of its applications
- Folliculotropic Mycosis Fungoides: Update on Diagnosis, Clinicopathological Stage, and Management
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Autosomal Ichthyosis with Hypotrichosis Syndrome Displays Low Matriptase Proteolytic Activity and Is Phenocopied in ST14 Hypomorphic Mice
- Autosomal recessive ichthyosis with hypotrichosis syndrome: further delineation of the phenotype
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i>
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Congenital and Hereditary Skin Diseases
- Congenital and Hereditary Skin Diseases
- Dermatological diseases from a genetic perspective
- Clinical report of a Holstein's calf with ichthyosis.
- Acquired hypertrichosis lanuginosa: Case report and review of the literature
- Management of congenital ichthyoses: European guidelines of care, part two
- Congenital atrichia and hypotrichosis
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Inherited Disorders of the Hair
- Skin barrier, phenotypic and genotypic characterisation of autosomal recessive ichthyosis in TGM1‐deficient Jack Russell Terriers and response to topical ceramide
- Bi-allelic Mutations in LSS, Encoding Lanosterol Synthase, Cause Autosomal-Recessive Hypotrichosis Simplex
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- The urine as a diagnostic key for a homozygous EGFR mutation
- First Symposium of Ichthyosis Experts
- Uso actual de la vitamina D en dermatología
- Disorders of hair in children