Disease: Epidermolysis bullosa simplex with mottled pigmentation
- A mutation in the V1 domain of keratin 5 causes epidermolysis bullosa simplex with mottled pigmentation
- A novel mutation and large size polymorphism affecting the V2 domain of keratin 1 in an African-American family with severe, diffuse palmoplantar keratoderma of the ichthyosis hystrix Curth-Macklin type
- A prospective, split-face, double-blinded, randomized study of the efficacy and safety of a fractional 1064-nm Q-switched Nd:YAG laser for photoaging-associated mottled pigmentation in Asian skin
- A transient epidermolysis bullosa simplex-like phenotype associated with bexarotene treatment in a G138E KRT5 heterozygote
- An additional case of epidermolysis bullosa simplex herpetiformis of Dowling-Meara with mottled pigmentation
- Analysis of <em>KRT5</em> and <em>KRT14</em> gene mutations and mode of inheritance in Iranian patients with clinical suspicion of Epidermolysis bullosa simplex
- Assessment of melanin distribution in epidermolysis bullosa simplex with mottled pigmentation: A case report
- Association of Epidermolysis Bullosa Simplex With Mottled Pigmentation and EXPH5 Mutations
- Clinical heterogeneity of 1649delG mutation in the tail domain of keratin 5: a Japanese family with epidermolysis bullosa simplex with mottled pigmentation
- Diffuse partial woolly hair in a patient with epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis Bullosa Simplex
- Epidermolysis bullosa simplex and mottled pigmentation: a new dominant syndrome. I. Clinical and histological features
- Epidermolysis bullosa simplex clearance after nasopharyngeal carcinoma treatment
- Epidermolysis bullosa simplex herpetiformis of Dowling-Meara with mottled pigmentation: the relationship between EBS herpetiformis and EBS with mottled pigmentation
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex with mottled pigmentation
- Epidermolysis bullosa simplex with mottled pigmentation - mutation analysis proved the diagnosis in a four-generation pedigree
- Epidermolysis bullosa simplex with mottled pigmentation due to a rare keratin 5 mutation: cutaneous findings in infancy
- Epidermolysis bullosa simplex with mottled pigmentation due to de novo P25L mutation in keratin 5 in an Italian patient
- Epidermolysis bullosa simplex with mottled pigmentation resulting from a recurrent mutation in KRT14
- Epidermolysis bullosa simplex with mottled pigmentation with noncicatricial alopecia: identification of a recurrent p.P25L mutation in KRT5 in four affected family members
- Epidermolysis bullosa simplex with mottled pigmentation: a case report
- Epidermolysis bullosa simplex with mottled pigmentation: a family report and review
- Epidermolysis bullosa simplex with mottled pigmentation: a novel KRT14 mutation
- Epidermolysis bullosa simplex with mottled pigmentation: clinical aspects and confirmation of the P24L mutation in the KRT5 gene in further patients
- Epidermolysis Bullosa Simplex with mottled pigmentation: mutation analysis in the first reported Hispanic pedigree with the largest single generation of affected individuals to date
- Epidermolysis bullosa simplex with mottled pigmentation: the first Slovenian case
- Epidermolysis bullosa simplex with mottled pigmentation. Case report and review of the literature
- Epidermolysis bullosa simplex: expression of gelatinase activity in cultured human skin fibroblasts
- Exon 8 deletion of KRT5 in epidermolysis bullosa simplex with mottled pigmentation: A case report
- Gene expression analysis of epidermolysis bullosa simplex with mottled pigmentation
- Human keratin diseases: hereditary fragility of specific epithelial tissues
- Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype
- Keratotic lesions in epidermolysis bullosa simplex with mottled pigmentation
- Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation
- Mutation analysis in the family of a Taiwanese boy with with epidermolysis bullosa simplex dowling-meara
- Mutation analysis of keratin 5 and keratin 14 genes in a family with epidermolysis bullosa simplex with mottled pigmentation
- Mutational analysis on 16 Japanese population cases with epidermolysis bullosa simplex
- Natural course of epidermolysis bullosa simplex with mottled pigmentation in a Japanese family with the p.P25L mutation in KRT5
- Novel keratin 5 and 14 gene mutations in patients with epidermolysis bullosa simplex from Poland
- One novel and two recurrent mutations in the keratin 5 gene identified in Chinese patients with epidermolysis bullosa simplex
- Recurrent p.N767S mutation in the ATP2A2 gene in a Japanese family with haemorrhagic Darier disease clinically mimicking epidermolysis bullosa simplex with mottled pigmentation
- Sporadic form of epidermolysis bullosa simplex with mottled pigmentation
- The genetic basis of epidermolysis bullosa simplex with mottled pigmentation
- The P25L mutation in the KRT5 gene in a Japanese family with epidermolysis bullosa simplex with mottled pigmentation
- Two novel recessive mutations in KRT14 identified in a cohort of 21 Spanish families with epidermolysis bullosa simplex