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Research 31–60 of 679
- Clouston’s Syndrome-A Case Report
- KRT16 wt Allele
- Cirmcumscribed juvenile pityriasis rubra pilaris in a 5-year-old-girl treated with topical keratolytic and steroid
- STUDY OF CUTANEOUS MANIFESTATIONS IN THYROID DISORDERS
- Disorders of Keratinization
- Woolly Hair in Two Siblings
- Olmsted syndrome
- Dysfunction of keratinocyte adhesion
- P029 A case of atypical bullous pemphigoid
- Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
- Olmsted Syndrome Caused by a Heterozygous p.Gly568Val Missense Mutation in <i>TRPV3</i> Gene
- PA05 A rare case of cardiocutaneous syndrome in a young child
- Two‐Year Follow‐Up of Ectodermal Dysplasia‐Syndactyly Syndrome 1 in a Palestinian Child Successfully Treated With Topical Minoxidil and Tretinoin: A Case Report
- [Acitretine].
- Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b
- Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa
- Spiny Keratoderma
- Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i>
- Regulation of Keratin 9 in Nonpalmoplantar Keratinocytes by Palmoplantar Fibroblasts Through Epithelial–Mesenchymal Interactions
- Botulinum Toxin Off-Label Use in Dermatology: A Review
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma
- Editorial: Exploring innovative therapies for rare inflammatory skin diseases
- Nagashima-Type Palmoplantar Keratosis: A Common Asian Type Caused by SERPINB7 Protease Inhibitor Deficiency
- REVIEW OF SO-CALLED ASEPTIC NEUTROPHILIC DERMATOSES
- <i>GJB6</i> missense variant in a Labrador Retriever with paw pad hyperkeratosis
- Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation
- Clouston’s syndrome: a rare case report
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Oral retinoids-present status