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5. Epidermolysis bullosa simplex with mottled pigmentation due to a rare keratin 5 mutation: cutaneous findings in infancy. Geller L, Kristal L, Morel KD. Pediatr Dermatol; 2013 Aug; 30(5):631-2. PubMed ID: 23889190 [Abstract] [Full Text] [Related]
6. Epidermolysis bullosa simplex with mottled pigmentation. Case report and review of the literature. Combemale P, Kanitakis J. Dermatology; 1994 Aug; 189(2):173-8. PubMed ID: 8075449 [Abstract] [Full Text] [Related]
7. Lethal epidermolytic epidermolysis bullosa: a new autosomal recessive type of epidermolysis bullosa. Salih MA, Lake BD, el Hag MA, Atherton DJ. Br J Dermatol; 1985 Aug; 113(2):135-43. PubMed ID: 4027181 [Abstract] [Full Text] [Related]
8. Autosomal dominant epidermolysis bullosa dystrophica: are the Cockayne-Touraine, the Pasini and the Bart-types different expressions of the same mutant gene? Bouwes Bavinck JN, van Haeringen A, Ruiter D, van der Schroeff JG. Clin Genet; 1987 Jun; 31(6):416-24. PubMed ID: 3621647 [Abstract] [Full Text] [Related]
9. Epidermolysis Bullosa Simplex with mottled pigmentation: mutation analysis in the first reported Hispanic pedigree with the largest single generation of affected individuals to date. Shurman D, Losi-Sasaki J, Grimwood R, Kivirikko S, Tichy E, Uitto J, Richard G. Eur J Dermatol; 2006 Jun; 16(2):132-5. PubMed ID: 16581562 [Abstract] [Full Text] [Related]
10. Molecular confirmation of the unique phenotype of epidermolysis bullosa simplex with mottled pigmentation. Irvine AD, Rugg EL, Lane EB, Hoare S, Peret C, Hughes AE, Heagerty AH. Br J Dermatol; 2001 Jan; 144(1):40-5. PubMed ID: 11167681 [Abstract] [Full Text] [Related]
11. Epidermolysis bullosa simplex superficialis. A new variant of epidermolysis bullosa characterized by subcorneal skin cleavage mimicking peeling skin syndrome. Fine JD, Johnson L, Wright T. Arch Dermatol; 1989 May; 125(5):633-8. PubMed ID: 2653224 [Abstract] [Full Text] [Related]
12. Pretibial epidermolysis bullosa: report of two families and review of the literature. García-Pérez A, Carapeto FJ. Dermatologica; 1975 May; 150(2):122-8. PubMed ID: 1158004 [Abstract] [Full Text] [Related]
15. Epidermolysis bullosa simplex with mottled pigmentation due to de novo P25L mutation in keratin 5 in an Italian patient. Pascucci M, Posteraro P, Pedicelli C, Provini A, Auricchio L, Paradisi M, Castiglia D. Eur J Dermatol; 2006 Jul; 16(6):620-2. PubMed ID: 17229601 [Abstract] [Full Text] [Related]