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Research 31–60 of 1000+
- Harlequin ichthyosis (ichq): a juvenile lethal mouse mutation with ichthyosiform dermatitis.
- Erythroderma: clinical and etiological study of 88 cases seen in a tertiary hospital over 25 years
- <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy
- 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
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Hair and Nail Relationship
- Early Skin Biopsy in Conradi‐Hünermann‐Happle Syndrome (X‐Linked Dominant Chondrodysplasia Punctata)
- Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities
- Ichthyosis
- AN UPDATE OF HAIR SHAFT DISORDERS
- Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice
- A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome
- Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines
- Hair Shaft Dysplasias
- Diseases of Periocular Hair
- Immunological control of skin development: from homeostasis to developmental pathologies
- Madarosis
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- Keratitis-Ichthyosis-Deafness Syndrome Caused by Missense Mutation in GJB2 Encoding Connexin 26 in a Chinese Patient
- Rickets in association with skin diseases and conditions: A review with emphasis on screening and prevention
- Dupilumab in a 9-week-old with Netherton Syndrome Leads to Deep Symptom Control
- 075 Clinical investigation of JAK inhibitor Tofacitinib in scarring alopecias
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome