Disease: Keratoderma palmoplantaris transgrediens
- A Sporadic Case of Mal de Meleda Caused by Gene Mutation in SLURP-1 in Korea
- Clinical and genetic studies of 3 large, consanguineous, Algerian families with Mal de Meleda
- Cutaneous paraneoplasia
- Familial coexistence of erythrokeratodermia variabilis and keratosis palmoplantaris transgrediens et progrediens
- Identification of novel homozygous SLURP1 mutation in a Javanese family with Mal de Meleda
- Keratosis extremitatum (Greither's disease): clinical features, histology, ultrastructure
- Keratosis palmoplantaris varians of Wachters
- Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates
- Mal de Meleda: genetic haplotype analysis and clinicopathological findings in cases originating from the island of Mljet (Meleda), Croatia
- Mal de Meleda: recessive transgressive palmoplantar keratoderma with three unusual facultative features
- Nail changes in Meleda disease
- Neutral lipid storage disease with unusual presentation: report of three cases
- Palmoplantar keratoderma, oral involvement, and homozygous CTSC mutation in two brothers from Cambodia
- Patient with Mal de Meleda in whom a Novel Gene Mutation was Identified
- Recessive keratosis palmoplantaris progrediens (Meleda's disease)