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Research 91–120 of 822
- Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership
- Missense mutation Y449H of the K10 gene in a patient with severe epidermolytic ichthyosis
- Acquired ichthyosis, alopecia and loss of hair pigment associated with leiomyosarcoma.
- LAMELLAR ICHTHYOSIS: ONE CASE REPORT
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Collodion baby to bathing suit ichthyosis: A 6-year follow-up
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Surgical approach of ectropion in lamellar ichthyosis
- Acquired ichthyosis, alopecia and loss of hair pigment associated with leiomyosarcoma
- Role of cholesterol sulfate in epidermal structure and function: Lessons from X-linked ichthyosis
- Identification of a novel<i>PNPLA1</i>mutation in a Spanish family with autosomal recessive congenital ichthyosis
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Male-Pattern Baldness in Men with X-Linked Recessive Ichthyosis
- A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family
- Absence of Male-Pattern Baldness in Men with X-Linked Recessive Ichthyosis?
- Substrate specific sulfatase activity from hair follicles in recessive X-linked ichthyosis
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- Steroid-resistant nephrotic syndrome associated with steroid sulfatase deficiency—x-linked recessive ichthyosis: a case report and review of literature
- Male-Pattern Baldness Is Common in Men with X-Linked Recessive Ichthyosis
- Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study
- Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis
- NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis
- 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis
- 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
- Prenatal Screening for Bathing-suit Ichthyosis After Diagnosis in an Older Sibling
- Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants
- Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis
- Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection